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<![CDATA[Are you an EPA Certified Lead-Based Paint Inspector or Risk Assessor? A NYSDOL-Certified Asbestos Inspector, Investigator, Project Monitor or Air Sampling Technician? We are seeking individuals with current environmental certifications to join our team as environmental field inspectors. Our ideal candidate: EPA Certified Lead-Based Paint Inspector or Risk Assessor NYSDOL-Certified Asbestos Inspector 1-3+ years of experience performing environmental field inspections Knowledge and finesse of the NYC mass transit system A proven track record showing responsibility and excellent references Great handwriting and no fear of paperwork Dedicated, able to follow instructions and possessing strong decision-making and communication skills High Energy Job Description: Conducting environmental field inspections within the 5 boroughs of New York City. Inspectors coordinate with building supers to obtain access to testing areas, collect environmental samples, record observations and fill out paperwork. Samples and forms are then returned to our offices at the close of the day. We are currently interviewing candidates with valid certifications and some field experience, but if your experience, education and interests are related we may consider your credentials. Please email resumes and cover letters (in-email cover letters are OK). Emails should reference "CL-Inspector" in the subject line. Any mislabeled or unlabeled emails will be deleted immediately. This is a full-time position and we want you to start immediately! We are a close-knit team and our best inspectors enjoy unparalleled job security and a strong family atmosphere.]]>

<![CDATA[Our small, busy and bustling New York City environmental consulting firm is seeking a self-motivated, highly dedicated individual with an outstanding and proven work ethic to assist us! We are currently seeking an experienced Environmental Professional to perform and prepare ASTM Phase I Environmental Site Assessments (Phase 1 ESAs). Duties required with this position include; frequent communication with clients, customer service, managing multiple project duties, billing, managing large, high volume, high profile clients. The ideal candidate should be well organized, proficient in all Microsoft Office applications, capable of handling multiple duties and projects, be a good written and verbal communications, detail oriented, capable of completing tasks on a tight time schedule, and be comfortable working independently. Qualifications as an "Environmental Professional" in accordance with the ASTM Phase I standard is a big plus. We have full time and part time (project by project basis) work and we want you to start immediately! We are a close-knit team and our best employees enjoy unparalleled job security and a strong family atmosphere. We are currently seeking candidates with 3-5 years experience preparing Phase I ESA reports as an EP but will interview candidates with 1-3 years preparation experience as an EP. Resumes and Cover Letters should be sent via email with the text "CL-ESA" in the subject line.]]>

<![CDATA[ZEBRAFISH AQUACULTURE RESEARCH TECHNICIAN (NEW YORK CITY) The Zebrafish Aquaculture Facility at New York University School of Medicine has a position available for a Zebrafish Aquaculture Research Technician starting October 2010 (the starting date is flexible but no later than November 15/2010). This technician will join a team of two technicians to support research in zebrafish in the laboratories of Drs. Holger Knaut and Jesús Torres-Vázquez at the Skirball Institute of Biomolecular Medicine. Responsibilities include: oversight of our 1000 sq. ft. 3500-tank zebrafish aquaculture facility, breeding and rearing zebrafish, maintenance/repair of the water system and assistance with experiments investigating the genetic regulation of zebrafish development. ELIGIBILITY (please apply only if you meet all of the criteria below): 1. B.S. or M.S. in Biology, Fisheries or related fields (obtained in the last five years) 2. Availability to start this position between October 1 and November 15/2010 3. Commitment to the job for at least two years 4. Highly desired attributes include: a) Aquaculture experience b) Plumbing and/or electrical hands on knowledge c) Research experience 5.Excellent time management, leadership, verbal and written communications skills are essential as the position includes both teamwork and independent tasks, and involves communicating with members of the two zebrafish laboratories and with the NYU Facilities/Maintenance staff. NYU School of Medicine offers an excellent salary and benefits package including four weeks paid vacation and tuition remission at NYU. Therefore, this position is ideal for someone who would like to pursue a Master in Biology or a related field. TO APPLY Send e-mail using the subject line: “2010 Zebrafish technician: your name", sending your CV as a single WORD document or PDF file that starts with the following information: 1. Name, current living address (city and country) and telephone number. 2. Expected date of availability. 3. Degree, date awarded and GPA. 4. Name, title, e-mail and phone number of three references (state in what capacity these references know you).]]>

<![CDATA[The Department of Psychiatry is seeking a Senior Project Manager to oversee several research studies including: Prospective Study of Posttraumatic Stress in Police Officers, a longitudinal study of police officers recruited from New York and three Bay Area police departments; Biomarkers Study of PTSD in OEF/OIF Veterans, a 2 year multi-site biological study to identify markers of PTSD; and Anxiety Reduction Treatment for Acute Trauma, a pilot brief intervention study of acute trauma administered at the Bellevue ER following an accident or physical assault. The incumbent will oversee the design and implementation of the study methods, as well as oversee and monitor the daily operations of study implementation. The incumbent will recruit, train and supervise a staff of research assistants, diagnostic evaluators and other support staff. Essential Functions: Recruit, train and supervise research assistants, diagnostic evaluators and research psychotherapists; Develop recruitment and project materials including modification of treatment manuals, participant hand-outs, subject recruitment materials and self-report questionnaire booklets; Develop manualized procedures for studies; Prepare and submit all IRB materials; Develop project infrastructure in close coordination with NYUMC and multi-sites involved in the research studies; Oversee and review data management and transmission; Participate in grant and manuscript preparation; Participate in executive meetings concerned with program-wide administration; Other duties as assigned. Job Requirements: PhD in Clinical Psychology preferred and MA in Clinical Psychology or project management considered with a minimum of 2 years postdoctoral research experience; Prior experience in coordinating multi-site clinical research studies; Applicants require extensive experience with IRB protocols, human subject compliance, data safety and monitoring, supervision of research assistants, recruitment and retention of research participants, subject tracking databases, manualization of biological and behavioral procedures in translational clinical research, data acquisition and data transfer protocols, data entry and validation, preparation of progress reports for funding agencies, storage and retrieval of complex data sets, generation of figures and tables, basic skills in pre-award and post-award budgeting, ensuring that project milestones are achieved, assistance with conference presentation software, grant and manuscript preparation, and related skills. ]]>

<![CDATA[Immediate, Part-time, Virtual: Use your interest, knowledge, and research skills to earn between $5,000 and $50,000 per research project. Earn potential rewards for uncovering scientific technical documents and develop valuable research experience. Article One Partners is the world’s largest patent research community. Article One posts requests for articles, patents, research papers, product literature, or any publicly available document in any language from anywhere in the world that describes particular technologies as of a specific date. These research postings are called Patent Studies, and the requested information is known formally as prior art. Article One’s global research community submits prior art in response to the posted Studies. By researching and submitting prior art, Article One’s registered members or Researchers become eligible to receive the stated reward. Rewards are distributed when Article One determines that a Researcher’s submission best matches the requirements of the Study as stated in the Study description. Anyone can join Article One’s global research community. Register as a Researcher at <a href="http://www.articleonepartners.com" rel="nofollow">http://www.articleonepartners.com</a> and begin working on these and other Studies: • Two-Sided Printable Media ($5,000) • Method of Manufacturing: Semiconductor Devices ($5,000) • Data Processing Device: Semiconductor Chip ($5,000) • Adding Function to a Web Page ($10,000) • Communication of Selected Information ($20,000) • Hydraulic Gear Pump Having Sound Absorption Cavities ($15,000) • Dynamic Power Management Device ($10,000) • Wireless Device: Multi-Function Communicator ($5,000) Article One will review all submissions and inform you if you have earned the stated reward. Your active participation on Article One will earn points for profit-sharing, as described on our website. For more information or to register as a Researcher, visit <a href="http://www.articleonepartners.com" rel="nofollow">http://www.articleonepartners.com</a> When registering, please enter the referral code “craig.”]]>

<![CDATA[“Patients First” isn’t just our tagline; it’s the way we live —every day. We’re Dendreon, and we’re fighting cancer, cell by activated cell, using a radical new approach: Active Cellular Immunotherapy, which empowers the body’s defenses by activating T-cells to battle this pernicious foe in an entirely new way. And when you join our team, you’ll have opportunity to build a career using advanced scientific techniques, new to our industry. In our QA - Quality Systems (sometimes referred to as Compliance) department you’ll participate in a fast-paced high volume production environment with high quality and regulatory standards. By driving thorough investigations, ensuring robust corrective and preventative actions, and real-time trending analysis you’ll further our efforts to ensure the patients we serve receive the highest standards of safety and quality. We’re developing a product that is first-in-kind; it’s like no other. We’re like no other. So you can expect to work with teams of colleagues who are passionate and driven to deliver their best work. And if you’re someone who prefers to work unique hours and four day work weeks, even three day work weeks, this could be a good fit. We also offer shift differentials! Here are some of the things you’ll do: • Participate in thorough investigations into producut failures using standard industry investigation tools (e.g., Root Cause Analysis, DMAIC, 5 Whys). • Provide site support for the following: - Change Control management and coordination with Corporate Quality Systems - Product Recalls - Biological Product Deviation Reports - Material Review Board and coordination with Corporate QA • Quarterly and Annual Management Review Reports and Annual Product Review • Perform tracking and trending of Quality metrics as part of Site Quality Committee and participate in Quality Council as requested. • Participate in Quality-on-the-Floor by developing strong working relationships with partners in Operations and providing real-time input to developing issues. More experienced individuals may also: • Participate in internal audits and regulatory inspections. • Provide leadership and mentorship to lesser-seasoned associates. Driven to make a difference in the lives of cancer patients? Looking for a career that will challenge and reward you in entirely new ways? Join us, and you’ll help shape this company’s future. And at the end of every day, you’ll know that you gave your best to help our cancers patient’s lives. Sound good? Let’s meet. Requirements: For Associate levels I/II -Bachelor’s degree in a scientific discipline or equivalent. -Typically 1 year related experience in cGMP/FDA regulated industry. -Prior experience working in recombinant protein, vaccine or bio-pharmaceutical manufacturing preferred. -Experience with investigations in cGMP/FDA regulated industry -Proficiency in MS Office applications. -Experience with ERP and/or MRP systems preferred. -Parental and/or cellular therapies preferred. Knowledge of cGMP/QSR and FDA device/drug/biologics regulations Additional for more senior level: -Typically 5 years experience in quality assurance, quality control, compliance, or manufacturing of commercial bio/pharmaceutical. Candidates will be placed based on experience, education, relevant skill set, and business need. Quality Assurance Associate I/II and Sr. Quality Assurance Associate I/II Working Conditions & Physical Requirements: -Ability to gown and work in a clean room environment -Travel 5 - 10% of the time -Lift up to 25 lbs. -May be required to work alternate shifts. The preceding job description has been designated to indicate the general nature and level of work performed by employees within this classification. Additional and incidental duties related to the primary duties may be required for company business needs from time to time. For more information and to apply for this position please visit <a href="http://www.dendreonjobs.com/" rel="nofollow">http://www.dendreonjobs.com/</a> Dendreon is an equal opportunity employer promoting diversity in the workplace. ]]>

<![CDATA[“Patients First” isn’t just our tagline; it’s the way we live —every day. We’re Dendreon, and we’re fighting cancer, cell by activated cell, using a radical new approach: Active Cellular Immunotherapy, which empowers the body’s defenses by activating T-cells to battle this pernicious foe in an entirely new way. And when you join our team, you’ll have opportunity to build a career using advanced scientific techniques, new to our industry. In our Quality Control Microbiology department you’ll assist with a variety of process from product testing, environmental monitoring, raw material testing and general laboratory maintenance. This is a fast-paced, highly technical environment with very high standards. We’re developing a product that is first-in-kind; it’s like no other. We’re like no other. So you can expect to work with teams of colleagues who are passionate about ensuring the patients we serve receive the highest standards of safety and quality. And if you’re someone who prefers to work unique hours and four day work weeks, this could be a good fit. We also offer shift differentials! Here are some of the things you’ll do. • Perform in-process and final product testing of Dendreon products using some of the following techniques: endotoxin, gram stain, and sterility by BacT/Alert. • Perform air viable monitoring (SAS), particulate monitoring (Met One), viable surface sampling and growth promotion testing of raw materials. • Receive and maintain test samples, reagents and reference standards used in the laboratory ensuring a well documented and approved process is followed. • Collaborate with Corporate Quality Control team members and contribute to the implementation of harmonized laboratory control systems in our Microbiology Laboratories. More experienced individuals may: • Act as Subject Matter Expert; leading, mentoring and training other associates in clean room behavior, aseptic process techniques, GMP documentation, quality systems and safety, etc. • May be responsible for direct QC oversight in the absence of the shift supervisor. • Actively monitor, coordinate, and execute timely completion of process documentation • Assist supervisors and Quality Assurance with identifying and documenting process deviations, change controls, and corrective actions (CAPA’s). • Assist supervisors with document revisions (SOP’s and batch records). • Assist supervisors and Manufacturing colleagues with corrective actions. • Develop innovative ideas for process improvement. • Collaborate with department in cross-functional teams, projects and GMP-related problem resolution and troubleshooting. • Track, trend, and report out on department specific metrics as requested Requirements: • Associate’s, Medical Technical, or life sciences degree or equivalent level of education and/or experience. • For entry level, experience with any of the above referenced lab techniques. GMP/FDA regulated industry preferred, but not required. • For more senior level, typically 4-6 years related experience in GMP/FDA regulated industry • Experience with computerized systems, like LIMS and knowledge of cGMP/ICH/FDA regulations are very desirable for these roles. • Proficiency in MS Office applications. • Candidates will be placed based experience, education, relevant skill set, and business need. Quality Control I/II and Sr. Quality Control Associate I/II Working Conditions & Physical Requirements: • Extensive use of laboratory equipment, chemicals and biological materials. • May require ability to gown aseptically for work in Clean Room environments. • May be required to work alternate shifts. Driven to make a difference in the lives of cancer patients? Looking for a career that will challenge and reward you in entirely new ways? Join us, and you’ll help shape this company’s future. And at the end of every day, you’ll know that you gave your best to help our cancers patient’s lives. Sound good? Let’s meet. For more information and to apply for this position please visit <a href="http://www.dendreonjobs.com/" rel="nofollow">http://www.dendreonjobs.com/</a> Dendreon is an equal opportunity employer promoting diversity in the workplace. ]]>

<![CDATA[“Patients First” isn’t just our tagline; it’s the way we live —every day. We’re Dendreon, and we’re fighting cancer, cell by activated cell, using a radical new approach: Active Cellular Immunotherapy, which empowers the body’s defenses by activating T-cells to battle this pernicious foe in an entirely new way. And when you join our team, you’ll have opportunity to build a career using advanced scientific techniques, new to our industry. In our aseptic manufacturing department you’ll produce products to the highest standards. So you can expect to work with teams of colleagues who are passionate about ensuring the patients we serve receive the highest standards of safety and quality. And if you’re someone who prefers to work unique hours and four day work weeks, this could be a good fit. We also offer shift differentials! Here are some of the things you’ll do. • Aseptic GMP manufacturing of clinical and commercial human blood therapeutics in a clean-room environment with biological safety cabinets Clean rooms are considered class ISO 5 or class 100 • Weigh, measure, and check raw materials to ensure batches manufactured contain proper ingredients and quantities. • Maintain standard operating procedures (SOP’s), batch records, and other applicable documentation to comply with regulatory requirements and good manufacturing practices (GMP’s). • Assist the validation department in executing applicable protocols effecting the manufacturing equipment or environment. More experienced individuals may: • Act as Subject Matter Expert; leading, mentoring and training other associates in clean room behavior, aseptic process techniques GMP documentation , quality systems and safety safety, etc. • May be responsible for direct manufacturing oversight in the absence of the shift supervisor. • Actively monitor, coordinate, and execute timely completion of process documentation • Assist supervisors and Quality Assurance with identifying and documenting process deviations, change controls, and corrective actions (CAPA’s). • Assist supervisors with document revisions (SOP’s and batch records). • Execute corrective actions and develops innovative ideas for process improvement. • Collaborate with department in cross-functional teams, projects and GMP-related problem resolution and troubleshooting. • Track, trend, and report out on department specific metrics as requested Requirements: • Associate’s, Medical Technical degree, life sciences degree or equivalent level of education and/or experience. • For entry level, experience with aseptic processing and / or in a GMP/FDA regulated industry preferred, but not required. • For more senior level, typically 4-6 years related experience in GMP/FDA regulated industry • Proficiency in MS Office applications. • Candidates will be placed based experience, education, relevant skill set, and business need. Cell Associate Positions: Manufacturing Associate I / II, Sr. Manufacturing Associate I / II (Lead) Working Conditions & Physical Requirements: Driven to make a difference in the lives of cancer patients? Looking for a career that will challenge and reward you in entirely new ways? Join us, and you’ll help shape this company’s future. And at the end of every day, you’ll know that you gave your best to help our cancers patient’s lives. Sound good? Let’s meet. For more information and to apply for this position please visit <a href="http://www.dendreonjobs.com/" rel="nofollow">http://www.dendreonjobs.com/</a> Dendreon is an equal opportunity employer promoting diversity in the workplace. ]]>

<![CDATA[“Patients First” isn’t just our tagline; it’s the way we live —every day. We’re Dendreon, and we’re fighting cancer, cell by activated cell, using a radical new approach: Active Cellular Immunotherapy, which empowers the body’s defenses by activating T-cells to battle this pernicious foe in an entirely new way. And when you join our team, you’ll have opportunity to build a career using advanced scientific techniques, new to our industry. In our Quality Control Bioassay department you’ll assist with a variety of process from product testing, raw material testing and general laboratory maintenance. This is a fast-paced, highly technical environment with very high standards. We’re developing a product that is first-in-kind; it’s like no other. We’re like no other. So you can expect to work with teams of colleagues who are passionate about ensuring the patients we serve receive the highest standards of safety and quality. And if you’re someone who prefers to work unique hours and four day work weeks, this could be a good fit. We also offer shift differentials! Here are some of the things you’ll do. • Perform in-process and final product testing of Dendreon products using some of the following techniques: flow cytometry, ELISA, endotoxin, gram stain, complete blood count, and viability. • Receive and maintain test samples, reagents and reference standards used in the laboratory ensuring a well documented and approved process is followed. • Collaborate with Corporate Quality Control team members and contribute to the implementation of harmonized laboratory control systems in our Bioassay Laboratories. More experienced individuals may: • Act as Subject Matter Expert; leading, mentoring and training other associates in GMP documentation, quality systems and safety, etc. • May be responsible for direct QC oversight in the absence of the shift supervisor. • Actively monitor, coordinate, and execute timely completion of process documentation • Assist supervisors and Quality Assurance with identifying and documenting process deviations, change controls, and corrective actions (CAPA’s). • Assist supervisors with document revisions (SOP’s and batch records). • Assist supervisors and Manufacturing colleagues with corrective actions. • Develop innovative ideas for process improvement. • Collaborate with department in cross-functional teams, projects and GMP-related problem resolution and troubleshooting. • Track, trend, and report out on department specific metrics as requested Requirements: • Associate’s, Medical Technical, or life sciences degree or equivalent level of education and/or experience. • For entry level, experience with any of the above referenced lab techniques. GMP/FDA regulated industry preferred, but not required. • For more senior level, typically 4-6 years related experience in GMP/FDA regulated industry • Experience with computerized systems, like LIMS and knowledge of cGMP/ICH/FDA regulations are very desirable for these roles. • Proficiency in MS Office applications. • Candidates will be placed based experience, education, relevant skill set, and business need. Quality Control I/II and Sr. Quality Control Associate I/II Working Conditions & Physical Requirements: • Extensive use of laboratory equipment, chemicals and biological materials. • May require ability to gown aseptically for work in Clean Room environments. • May be required to work alternate shifts. Driven to make a difference in the lives of cancer patients? Looking for a career that will challenge and reward you in entirely new ways? Join us, and you’ll help shape this company’s future. And at the end of every day, you’ll know that you gave your best to help our cancers patient’s lives. Sound good? Let’s meet. For more information and to apply for this position please visit <a href="http://www.dendreonjobs.com/" rel="nofollow">http://www.dendreonjobs.com/</a> Dendreon is an equal opportunity employer promoting diversity in the workplace. ]]>

<![CDATA[<h2> Project Engineer ‘15’ (New York) – Job # 28096</h2> Position Description Primary responsibility to complete combo ESA/PCA field assignments to augment/benefit anticipated growth of real estate services department (HUD, Green M2M, special servicing, FDIC, agency lending, etc.); based, in part, on ~20% national sales budget increase in 2010 (approx. $2.5 million). Though the primary focus of the employment position is detailed above, EBI also looks to consider applicants with a diversified skill set that will benefit the future development of EBI as a whole; serving real estate, telecommunications, and institutional & industrial service clientele nationwide. Beneficial skill sets include, but not limited to: construction loan monitoring, Phase II subsurface investigation, remedial action planning, asbestos/lead inspection and abatement, Brownfield assessment, certified hazardous materials management (CHMM), emergency response, professional training provider, regulatory permitting, industrial hygiene, compliance audits, energy audits, and sustainability services. Staff and client management experience will also be evaluated. Registration Requirements Engineering consulting experience preferred; however specific registration credentials not required. Education/Experience Requirements 5 – 10 years experience in engineering consulting and/or B.S. in Engineering, Architecture, or Construction. Knowledge of HUD and/or other government-related work product preferred as well. Company History EBI Consulting, founded in 1989 to provide management consulting due diligence based on best technology and practices in Environmental Health & Safety. EBI has grown to $40 million in revenues in 2007 and is expected to exceed this in 2010. EBI has built three distinct and diversified businesses working for Real Estate (EB-RE), Telecom (EB-TC), Industrial & Institutional (EB-IIS) clients including the top names in these fields, such as Bank of America, JP Morgan, Morgan Stanley, Prudential, John Hancock, AT&T, Verizon, Sprint Nextel, Bechtel, General Dynamics, EMDSerono, Genzyme, Harvard University, Cambridge Hospital and hundreds more. One key to achieving this growth is to continue to recruit and retain people with exceptional technical and business management experience. We must then capitalize on their expertise by providing improved operating results for EBI's growing and diversified client base and business relationships. EBI Today Business Segments: <ul> <li>Real Estate- Engineering and environmental due diligence services including site assessments and engineering evaluations for real estate investors, mortgage bankers, and investment bankers. Clients include hundreds of most important commercial and investment banking companies and real estate owners and operators nationally. </li> <li>Telecommunications- Engineering and environmental due diligence for wireless carriers and tower companies for collocation and site development. EBI utilizes our diverse team resources, to provide full range of Architecture & Engineering, Radio-Frequency Electromagnetic Energy, and Environmental Health & Safety services. EBI delivers flexible, cost-efficient solutions. Clients include dozens of most important wireless companies and their general contractors such as Bechtel and General Dynamics. </li> <li>Institutional & Industrial Services- Full-service Environmental, Health & Safety and management consulting services assisting Healthcare, Life Sciences, and Manufacturing and Educational clients create business value through best-practices with compliance and permitting, risk management, and enterprise-wise sustainability programs. Clients include dozens of the most important companies and institutions in these growing areas. </li> </ul> The Opportunity EBI Consulting has grown by 30% to 50% in nine of the last twelve years, always profitable and cash positive. This includes two years of $10 million growth (50% & 33%) and one year of $5 million (35%). Similar growth is planned for 2010 and beyond bringing revenues to $50 million by 2013 and $100 million in this decade. Based on the diversity and quality of its client relationships and of its existing and planned management and technical capabilities, EBI Consulting is positioned better than ever to achieve this growth. Plans and Expectations for Future Growth for EBI EBI has implemented an aggressive plan to develop new business lines, acquire new clients, as well as invest in existing lines of business that have potential for significant growth. We work with and for our clients to provide Business Management Consulting to enable them to improve their profitability and marketability by implementing Environmental Health & Safety as well as other improvements. For more information about EBI and open positions please visit our website at www.ebiconsulting.com. What the Successful Candidate Should Anticipate We expect the successful candidate would work with our team to help EBI realize our goals while at the same time, the successful candidate will realize personal, professional and financial growth. Benefits EBI offers competitive compensation, bonus opportunities, group medical & dental insurance, 401k plan with employer contribution, tuition reimbursement, paid vacation, and progressive career opportunities. EOE M/W/D/V Submittal Please submit a resume and cover letter in Word or PDF format via email to <a href="mailto:jobs@ebiconsulting.com" rel="nofollow">jobs@ebiconsulting.com</a>. You must include the following information: <ul> <li>Reference job #, job title and resource </li> <li>Brief summary of past related experience (highlight your experience as it relates to our need & industry) </li> <li>List of your education credentials and professional registrations </li> <li>Salary history </li> </ul> We look forward to hearing from you!  ]]>

<![CDATA[Sovereign Consulting Inc., a rapidly growing environmental consulting and remediation firm headquartered in Robbinsville, NJ, is seeking Project Managers (10+ years experience) for its Farmingdale, NY location. Responsibilities will include: <ul><li>supervision and guidance of staff level positions & responsibilities;</li> <li>drilling, soil sampling and monitoring well installation supervision;</li> <li>collection of additional site characterization data and information;</li> <li>aquifer characterization and groundwater modeling;</li> <li>other contaminant fate & transport modeling;</li> <li>indoor air-quality evaluations and other exposure pathway and risk evaluations;</li> <li>evaluation, summary and comparison of site-specific characterization data to cleanup standards;</li> <li>preparation of Site Characterization Reports, Remedial Action Plans, other technical reports;</li> <li>adherence to Sovereign and Client Health & Safety Standards in all field-related activities. </li> <li>Client and Regulatory interaction to develop SCRs, RAPs and Closure Plans</li></ul> Prior experience with petroleum and non petroleum remediation sites, NYSDEC Regulations and Guidance are required. Qualified Environmental Professional a plus. Applicants with prior 40-Hour OSHA (29 CFR 1910.120) HAZWOPER health and safety training and current 8-hour refresher are preferred. Assigned position responsibilities will be commensurate with experience and include a variety of the responsibilities listed above as workload or client demands dictate. Successful candidates will be responsible, self-motivated individuals who are eager to take advantage of an excellent opportunity to work with one of the most highly regarded firms in the environmental consulting and site assessment / remediation business. Organizational skills and prior experience using Microsoft Office products is required. All applicants must have a clean driving record and High School diploma. An earth sciences related degree (geology, geophysics, geotechnical, or environmental) or a degree in a related major such as Mathematics/Physics, Civil or Mechanical Engineering, Construction Management, or Environmental and Occupational Safety, will be considered. A New York Professional license (PG or PE) may be required for certain position responsibilities. Prior experience working with soil/groundwater remediation systems would be helpful, but not required. Experience working with portable field instruments, including interface probes, water quality instrumentation, air/gas monitoring instruments, and portable GPS systems are helpful, but not required. Good mechanical skills and experience communicating with the general public, general contractors or construction managers is helpful. Task specific training will be provided for all job functions. Employment at Sovereign is contingent upon the results of a Drug & Alcohol screening test and a pre-placement medical evaluation that determines candidate’s ability to capably and safely perform the proposed job duties. Candidates must present documentation that confirms identity and eligibility for employment in the United States. Salary will be commensurate with experience. These full-time positions offer an excellent benefits package including: group healthcare program, vision and dental coverage plan, life and AD&D insurance plans, short & long-term disability programs, other supplemental insurance programs, 401(k) retirement plan, tuition reimbursement program, paid holidays and paid vacation. A relocation package will not be offered for these positions. Send resumes to hr@sovcon.com. EOE ]]>

<![CDATA[Seeking masters or postdoctoral level research scientist with a long term interest in developing strategies for recovery from brain injury or hemorrhage. Preferably this individual will have a neuroscience/developmental neurobiology background (Ph.D. or M.S.) and familiarity with cellular and molecular mechanisms of neurologic injury. A grant will fund this position for two years, but the person hired will be expected to pursue obtaining additional funding. Interested candidates should forward their cv and a one paragraph statement detailing their long term career interests to tbisearchnyu@yahoo.com. ]]>

<![CDATA[Independent retail pharmacy in the Bronx is seeking to hire a FULL TIME pharmacist. -We offer top salary and benefits that include 4 weeks vacation! Requirements include: -Must be able to work 5 times a week -At least 2 years of experience required -License & Registration in NYS is required -OPUS knowledge a plus -Business and Retail background is a plus -Bilingual: English and Spanish Dependability and punctuality required Feel free to fax your resumes to: 212-575-4625 ]]>

<![CDATA[CME Agency in midtown searching for Scientific Directors and Medical Writers Requirements: Advanced degree (PhD, MD, PharmD) 2-5yrs+ Medical Education agency experience Entrepreneurial sprit – willingness to assist in building the business High level of scientific & medical marketing knowledge that will generate credibility with KOLs and pharmaceutical clients Communication skills – ability to present difficult concepts clearly to sales team and clients Teamworking – desire to work in a team based culture with freelance medical writers, sales and project managers Ability to multi-task, work in a client service environment and manage projects within an allotted budget Responsibilities: Develops and manages of scientific program(s) that fall under his/her responsibility. Supervises the work of freelance medical writers ensuring that work is of acceptable quality and generated to time and budget Uses in-depth therapeutic knowledge to writes content where necessary Understands client marketing needs and develops scientific work that supports the client strategy and messaging platform Develops publication strategies and works with key opinion leaders on creating innovative symposia Travels (up to 25%) of time with sales team to develop new business and meet with clients Works with project managers and other company staff to ensure that client is satisfied with the quality of the product Depending on job level may have staff/budget management responsibility Please send resume or contact info to above email link. Keywords: CME - Medical Director - Medical Writer - Scientific Director - Program Director - Medical Editor - Medical Education - Medical Communications - Healthcare Communications - Continuing Medical Education - C.M.E. - Scientific Writer - Scientific Associate]]>

<![CDATA[Environmental Sampling Technician – Start Immediately! Leighton Associates, Inc. (LAI) is an established environmental consulting firm, founded in 1992 and operating throughout the greater New York City metropolitan area. We have an immediate need for an Environmental Sampling Technician. This is an excellent position for a new graduate, providing you training and hands-on experience in the environmental industry. Duties - Collection of air, soil, water, and similar samples - Worker exposure air monitoring for lead and other heavy metals - Compliance with OSHA and EPA regulations Requirements - Must reside within commutable distance from New York City. We do not relocate. - A Bachelors degree in Environmental Science or a related field is preferred. We will also consider students working toward their degree and highly motivated high school graduates with related work experience. - Must have a reliable vehicle and driver’s license in good standing - Comfortable working outdoors To Apply Please email your resume with desired compensation to the craigslist.org address or fax to 718-268-6317. We are an Equal Opportunity Employer. ]]>

<![CDATA[Now Hiring Weekend Warriors! Cell Processing Associate Alternate Shifts (all levels, I/II/Sr.) If activating T-cells activates your passion, we should talk. We’re Dendreon, and we’re fighting cancer, cell by activated cell, using a radical new approach: Active Cellular Immunotherapy, which empowers the body’s defenses to battle this pernicious foe in an entirely new way. We’re not just another biotech company; we actually live our purpose: putting patients first, every day. And when you join our team, you’ll see that we’re also building careers unlike any in the industry today. In our aseptic Manufacturing department, you’ll put your experience with cell-based development to work on a process that is revolutionary among biotech companies. You’ll help produce sterile, pyrogen-free products to the highest standards of purity and quality. These products will be infused in to our very important patients, so compliance will never be more critical. So you can expect to work with teams of colleagues who are fanatical (in a good way!) about preserving a sterile and efficient environment. Right now, we’re looking for motivated Alternate Shift Cell Processing Associates at every level to help us produce the highest standard of product for patients being treated with our immunotherapy prostate cancer vaccine. In this role, you’ll work as a weekend warrior, fighting cancer from 4 p.m. to 2 a.m. or 1:30am to 12:00pm, Friday through Monday, and be eligible for a great differential pay. You’ll keep to standard operating procedures and ensure error-free data entry to enable our Quality and other support groups to accurately assess, approve, and deliver final product to patients in a timely fashion. Some of the things you’ll be doing include: • Aseptically manufacture and assemble clinical and commercial human blood––derived components in a clean-room environment (Class 10,000/ISO7 and Class 100,000/ISO8). • Weigh, measure, and check raw materials to ensure proper ingredients and quantities. • Maintain records and clean-room environment to comply with regulatory requirements. • Assist in validating equipment and environments directly related to aseptic processing. • Provide general upkeep of gowning and supplies for the clean room in manufacturing areas. • Represent department in cross-functional teams, projects, and GXP-related problem resolution. Job Requirements: • Associate’s or medical technical degree or equivalent. • Typically one year of related experience in CGMP/FDA regulated industry. • Extensive use of laboratory equipment, chemicals, and biological materials. • Ability to gown aseptically. • Ability to lift 50 lbs. unassisted. Driven to make a difference in the lives of cancer patients? Looking for a career that will challenge and reward you in entirely new ways? Join us, and you’ll help shape this company’s future. And at the end of every day, you’ll know that you gave your best to help our cancers patient’s lives. Sound good? Let’s meet. Apply at: <a href="http://www.dendreonjobs.com/" rel="nofollow">http://www.dendreonjobs.com/</a> Fight Cancer. Make a Difference. Join Us.]]>

<![CDATA[SOFT Inc. is seeking a Laboratory Coordinator for its client in New York City on a contract basis. Duties: 1. Batching and picking up the specimen from Accessioning department. 2. Printing of TRFs and previous results if any and prepare folders a/c to the test type. Sending cases to other locations if needed. 3. Sort out specimens based on the Extraction types and prepare Extraction list for DNA and RNA. Also prepare Extraction worksheets that include entering reagent information and saving them in Molecular system. 4. Prepare Assay lists if applicable. 5. Prepare paraffin blocks for cutting (prepare label and sheet and decide the number of sections to be cut). 6. Return paraffin-blocks to shipping every week after the case is reported out. 7. Help finding the specimens that are scheduled for Molecular tests but not received on time (from Fresh Prep and Histology). 8. Keep previously tested specimen rotated in freezer, discard when necessary. 9. Help in Accessioning when needed. Skills: Microsoft Office, strong work ethic, works well within a team environment Education: Bachelor's Degree preferred but not required. At least 1 year of experience. ]]>

<![CDATA[The Quality Assurance Team of a specialty food importer and manufacturer of Mediterranean olives, antipasti and ingredients has an opening for an entry level position to assist with product testing, research, and documentation. Candidates responsibilities to include but not limited to: gathering product information, maintenance of detailed files of in-house (pH, salinity, and organoleptic) testing, research nutritional benefits and health claims, conduct nutritional comparisons, and ensure that all required certificates are up to date and organized. Additionally individual may be required to perform warehouse visits for gather samples and inspect damaged products. The candidate must be detailed oriented, highly organized, self motivated with an ability to work both independently and in a group setting. A clear and concise telephone manner is required and the candidate must be proficient with all aspects of Microsoft Office and Outlook and have the ability to learn new computer programs. A 4 year degree in Nutrition or Food Science is preferred and a passion for food is a must. Please forward your resume and a cover letter with your salary requirements. No telephone calls will be accepted. ]]>

<![CDATA[We are a small company that focuses on custom aquarium set up and maintenance. We are looking for ONE intern with a strong possibility of integrating into our business after 3 months of training. What we're looking for : MUST HAVE A COLLEGE DEGREE IN BIOLOGY OR RELATED FIELDS Knowledge of aquatic life and biology A passionate drive to learn about aquatic life Personal experience with fish tanks or aquariums are a plus Strong organizational skills Please forward your resume along with a cover letter ]]>

<![CDATA[Are you interested in part time consulting that allows you to set your own schedule? Do you have experience in Food Safety and Product Quality? Would you enjoy teaching and coaching in high energy atmospheres to improve the safety of restaurant kitchens? EcoSure, a division of Ecolab is seeking Field Specialists in New York . In our primary service, Food Safety Inspections, EcoSure partners with some of the largest restaurant, hotel and other foodservice chains in North America to enhance performance in food safety through evaluation, coaching and reporting. Field Specialists perform a wide variety of objective 3rd party quality assurance services, contributing to a safer environment for consumers, employees and children. In addition to Food Safety Evaluations, we also perform: • Product Quality Evaluations • Workplace Safety Evaluations • Playground Safety Audits • Food safety training classes to management and staff EcoSure will provide paid training to give you the skills needed for these opportunities. Field Specialists work as independent contractors and manage their own part time schedules. Candidates must not be currently working for a health department or regulatory body. Candidates living in the following areas will be considered: Manhattan Queens Jersey City/Newark/Staten Island Requirements: Bachelor’s Degree in Environmental Health, Food Science, Nutrition or related field Please email your resume or fax to the attention of Dana Rasof at (847) 597-9890 . ]]>

<![CDATA[PCI is growing! We are seeking a Technician for Electronic and Analytical Laboratory Instruments in support of our client. This position is full time with benefits, non-exempt, and up to 20% overnight travel is required. To Apply: <a href="http://pcijobs.iapplicants.com/ViewJob-100779.html" rel="nofollow">http://pcijobs.iapplicants.com/ViewJob-100779.html</a> DUTIES Expectations: The Staff Technician is charged with providing PCI clients with calibration, repair, and troubleshooting of analytical equipment and other instrumentation related services. The Staff Technician is expected to display working knowledge of company policies and procedures. Responsibilities/ Assignments: • Complete calibrations, qualifications, PM’s and repairs with accurate GxP documentation • Process calibration/qualification documentation in an accurate and timely manner. • Emergent repairs and troubleshooting • Locating and verifying equipment for PM • Ensure special client requests are conveyed to the appropriate PCI management resource and met in accordance with management direction. • Identify needs for additional supplies, equipment, etc. and convey to the appropriate management resource. • Must work to understand customer’s needs and requirements. QUALIFICATIONS Special Skills Required: • Understand basic concepts of calibration and calibration requirements including accuracy testing requirements • Understanding of electronics, instrumentation and controls, mechanical and electrical troubleshooting and repair skills • Understanding of chemistry, microbiology, separation methods, chromatography, spectroscopy and commonly used laboratory equipment • Operation of complex laboratory instruments such as HPLC, GC, Mass Spec, Dissolution, etc. • Operation of laboratory equipment such as balances, centrifuges, timers, micrometers, GE Akta equipment, incubators, etc. • Working knowledge of USP and EOP standards. • Understanding of safety requirements • General electrical panel knowledge and safety practices. • Working knowledge of MS Office products. • Experience with chromatography data gathering systems software (i.e. Millenium, TurboChrom, etc.) • Must have a valid driver’s license and good driving record. • Must be reliable, confident, eager to learn, and enjoy working with people. • Must be self-driven and demonstrate ability to work independantly and with little direction. Experience & Education Required: A four-year degree or higher in Chemistry, Life Sciences, or other related technical field such as Electronics or Engineering (or equivalent military training) and two years of instrumentation experience or the equivalent combination of the two. For more information, or to apply now, you must go to the website below. Please do not email your resume to us as we only accept applications through our website. <a href="http://pcijobs.iapplicants.com/ViewJob-100779.html" rel="nofollow">http://pcijobs.iapplicants.com/ViewJob-100779.html</a> ]]>

<![CDATA[ Obtains blood and non-blood specimens from Cancer Center and Infusion Center outpatients by venipuncture from the arm and/or microcollections from fingers in a variety of collection tubes or capillaries, some of which contain preservatives or anticoagulants. Assumes responsibility for actively contributing to section productivity and cost effectiveness. Assumes responsibility for recognizing situations that require referral to Laboratory Supervisor. Performs additional tasks as requested by Department Head or his/her designee. REQUIREMENTS: High school graduate with one year of training in a medical assisting program. EEO Since 1865, Saint Barnabas Medical Center (SBMC), located at 94 Old Short Hills Road in Livingston, is New Jersey’s oldest nonprofit, nonsectarian hospital. The 597-bed institution is one of the largest heath care providers in the state, treating more than 35,500 inpatients and over 84,000 Emergency Department patients each year. The Medical Center and the Saint Barnabas Ambulatory Care Center provide treatment and services for more than 300,000 outpatient visits annually. The Medical Staff is comprised of more than 1,600 physicians in 100 medical and surgical specialties and there are over 3,400 employees. As a teaching institution, we have nine residency programs and one fellowship in Mammography and a shared Nephrology fellowship with Newark Beth Israel. There are a total of 154 residents and fellows. Among Saint Barnabas’ nationally recognized facilities are The Burn Center, the only certified burn treatment facility in the state; the Saint Barnabas Health Care System Renal and Pancreas Transplant Division, one of the most active transplant programs in the country; The Saint Barnabas Heart Centers, a world-class cardiac surgery program in affiliation with Newark Beth Israel Medical Center; The Neurology and Neurosurgery Program which is the only program in New Jersey to be ranked by US News and World Report as a Top Hospital for Neurology and Neurosurgery.  It is lead by an unprecedented team of experts dedicated to diagnosing and treating disorders of the brain and nervous system; the Regional Perinatal Center, providing care for high-risk and critically ill infants in New Jersey’s leading Level III, a 56-bed Neonatal Intensive Care Unit; comprehensive Pediatric Services including a dedicated intensive care unit; The Bariatric Surgery Center of Excellence, designated by the American Society of Bariatric Surgery; a nationally accredited Chest Pain Center, The Center for Sleep Disorders; The Comprehensive Stroke Center at Saint Barnabas; extensive services in robotic and minimally-invasive surgery, The Institute for Reproductive Medicine and Science at Saint Barnabas, the widely recognized assisted reproductive technology program; and comprehensive cancer programs and services that includes one of the largest Radiation Oncology programs in northern New Jersey and a highly-specialized Gastrointestinal Cancer Center of Excellence.   To Apply for this position, please <a href="http://saintbarnabas.contacthr.com/16889376" rel="nofollow">CLICK HERE</a> ]]>

<![CDATA[ WEBSITE POSTINGS Standard Language to post along with IRB approved Poster or Flyer Graphic Birth Control Research Study- Put Away The Pills and Put On An Investigational Patch Eligible participants must: • be healthy women, 18-45 years of age; • have regular, consistent menstrual cycles between 25 and 35 days; • have no intention of becoming pregnant in the next 12 months; • be sexually active. We are seeking women who meet the above criteria for a research study. You will be paid for your time as well as receive free medical care and birth control. Please email simplify@nycwhr.com or call Kayee Yam, NP @ 646 290 9560]]>

<![CDATA[Individuals with extraordinary record of intellectual and professional achievement sought to work as Technical Operations and Project Management Lead within ambitious, well-funded scientific research group based in New York City. D. E. Shaw Research is pursuing long-term projects aimed at achieving major scientific advances in the fields of biochemistry and molecular biology. Among the group's current activities is the development of specialized supercomputers designed in part to fundamentally transform the process of drug discovery. The Technical Operations and Project Management Lead will perform in a high-impact, high-visibility capacity, and collaborate with technical team members to develop project plans and drive the group’s efforts forward. In addition to more traditional project management duties, this hire will work independently and with senior team members on a variety of strategic, risk-mitigation, and infrastructure projects. A technical background is desirable, but we also welcome non-technical candidates with exceptional intelligence and a willingness to quickly come up to speed in the hardware, computer science, and chemistry/biology spaces. Excellent communication skills and demonstrated leadership ability are critical. Three to five years experience managing technical projects and/or teams is a plus. We are prepared to reward exceptionally well-qualified individuals with above-market compensation. To submit an application, please use the link provided below: To submit an application, please use the link provided below: <a href="http://www.deshawresearch.com/recruit/jobs/Ads/Craigslist/TOL" rel="nofollow">http://www.deshawresearch.com/recruit/jobs/Ads/Craigslist/TOL</a> D. E. Shaw Research does not discriminate in employment matters on the basis of race, color, religion, gender, pregnancy, national origin, age, military service eligibility, veteran status, sexual orientation, marital status, disability, or any other protected class.]]>

<![CDATA[Position is available for a PLM ( Polarized Light Microscopy) analyst at an environmental laboratory ASAP. The position is available for some evenings and weekends. Interested candidates should have a college degree, experience in a laboratory setting, and MUST have knowledge of and experience with polarized light microscopy. Please do not respond if you do not meet these requirements. ]]>

<![CDATA[POSITION SUMMARY Reporting to the CEO, The VP CD will provide clinical leadership, strategic planning and scientific guidance and direct all clinical development efforts in collaboration with pharmaceutical industry partners to provide a cure for multiple myeloma. SUMMARY The ideal VP CD would be someone who is very knowledgeable about clinical trial design and management and who would feel comfortable collaborating at the highest levels with academic centers and thought leaders, the industry, the FDA, and other groups to use his or her influence and the resources of the Foundation to help choose suitable targets, guide the direction of myeloma research, drug development, and the approval process. The VP CD must also have the stature to be a candidate in the succession plan to become the company’s Chief Medical Officer. The person in this role will not only have the opportunity to influence the direction of future research efforts in myeloma, but also will be instrumental in directing the course of drug development to bring about dramatic improvements, and hopefully someday, a cure for multiple myeloma. JOB DESCRIPTION Annual Objectives Business: The VP CD will oversee the clinical aspects of the Personalized Medicine program in Multiple Myeloma, developing and implementing the operational plan. This plan consists of expanding the MMRC involvement additional academic as well as community-based centers The VP CD will identify and build relationships with thought leaders in the area of multiple myeloma including the FDA, NCI, ASH, ASCO, biotechnology and pharmaceutical clinical and research executives. The VP CD will work with executive management to demonstrate scientific credibility and business acumen to lead the efforts over the coming 5 years including but not limited to the development of 5 and 10-year business plans and the communication of clinical strategies within the company. The VP CD will work with the COO and CEO to ensure the alignment of current clinical efforts with overall company goals and strategies. The VP CD will guide the development of publications and presentations to communicate the achievements of the organization’s efforts to find a cure for multiple myeloma. The VP CD will oversee and work with the clinical development staff to ensure current research efforts are being performed efficiently and effectively, support the quality brand of the organization, are scientifically credible, meet enrollment and clinical research goals that are consistent with the long-term goals and strategies of the organization. People Through presence, confidence and mutual respect the VP CD will manage and provide guidance for all clinical research personnel to improve their personal credentials by initiating, supporting and assuring their efforts in the multiple myeloma community represent the organization’s brand. Personal Growth and Development The VP CD is responsible for identifying an optimal portfolio of clinical trials that speed drug development and maximize efficiencies. The VP CD will represent the organization at key scientific and non-profit meetings articulating the organization’s innovative business model, strategies and successes. Work directly with executive management to communicate priorities as they relate to the myeloma community, key opinion leaders, the Board of Directors and executive management of pharmaceutical and biotechnology companies. Quarterly Objectives Work with executive management to ensure cross-organizational communication of organizational objectives. Analyze clinical trial activities of pharmaceutical, biotechnology and academic institutions to ensure the organization’s clinical trial portfolio represents innovation and scientific value achieving the organization’s personalized medicine goals. Oversee global expansion efforts. Contribution to bottom line Establish priorities that have the greatest impact on myeloma patients to drive organizational success and subsequent investment revenue. Core customers and key relationships Pharmaceutical Executives FDA, NIH, NCI, ASH, ASCO Steering Committee and Project Review Committee Researchers Patients Staff Resources to Position People: Board of Directors, CEO, COO, CSO, Executive Director, Associate Director of Operations and staff, Staff Directors, and outsourced personnel. Manage the annual operating budget of $12 million. POSITION REQUIREMENTS · Medical degree (MD), or PharmD/PhD. · Oncology experience a plus. · Experience in pharmaceutical drug development. · Ability to build collaborations among key opinion leaders, national organizations, pharmaceutical and biotechnology organizations Contact: Bob Weinstein The Carolan Group Tel - 609-714-8947 Email RESUME/CV to LWEINST650@gmail.com]]>

<![CDATA[ POSITION SUMMARY Reporting to the CEO, The VP CD will provide clinical leadership, strategic planning and scientific guidance and direct all clinical development efforts in collaboration with pharmaceutical industry partners to provide a cure for multiple myeloma. SUMMARY The ideal VP CD would be someone who is very knowledgeable about clinical trial design and management and who would feel comfortable collaborating at the highest levels with academic centers and thought leaders, the industry, the FDA, and other groups to use his or her influence and the resources of the Foundation to help choose suitable targets, guide the direction of myeloma research, drug development, and the approval process. The VP CD must also have the stature to be a candidate in the succession plan to become the company’s Chief Medical Officer. The person in this role will not only have the opportunity to influence the direction of future research efforts in myeloma, but also will be instrumental in directing the course of drug development to bring about dramatic improvements, and hopefully someday, a cure for multiple myeloma. JOB DESCRIPTION Annual Objectives Business: The VP CD will oversee the clinical aspects of the Personalized Medicine program in Multiple Myeloma, developing and implementing the operational plan. This plan consists of expanding the MMRC involvement additional academic as well as community-based centers The VP CD will identify and build relationships with thought leaders in the area of multiple myeloma including the FDA, NCI, ASH, ASCO, biotechnology and pharmaceutical clinical and research executives. The VP CD will work with executive management to demonstrate scientific credibility and business acumen to lead the efforts over the coming 5 years including but not limited to the development of 5 and 10-year business plans and the communication of clinical strategies within the company. The VP CD will work with the COO and CEO to ensure the alignment of current clinical efforts with overall company goals and strategies. The VP CD will guide the development of publications and presentations to communicate the achievements of the organization’s efforts to find a cure for multiple myeloma. The VP CD will oversee and work with the clinical development staff to ensure current research efforts are being performed efficiently and effectively, support the quality brand of the organization, are scientifically credible, meet enrollment and clinical research goals that are consistent with the long-term goals and strategies of the organization. People Through presence, confidence and mutual respect the VP CD will manage and provide guidance for all clinical research personnel to improve their personal credentials by initiating, supporting and assuring their efforts in the multiple myeloma community represent the organization’s brand. Personal Growth and Development The VP CD is responsible for identifying an optimal portfolio of clinical trials that speed drug development and maximize efficiencies. The VP CD will represent the organization at key scientific and non-profit meetings articulating the organization’s innovative business model, strategies and successes. Work directly with executive management to communicate priorities as they relate to the myeloma community, key opinion leaders, the Board of Directors and executive management of pharmaceutical and biotechnology companies. Quarterly Objectives Work with executive management to ensure cross-organizational communication of organizational objectives. Analyze clinical trial activities of pharmaceutical, biotechnology and academic institutions to ensure the organization’s clinical trial portfolio represents innovation and scientific value achieving the organization’s personalized medicine goals. Oversee global expansion efforts. Contribution to bottom line Establish priorities that have the greatest impact on myeloma patients to drive organizational success and subsequent investment revenue. Core customers and key relationships Pharmaceutical Executives FDA, NIH, NCI, ASH, ASCO Steering Committee and Project Review Committee Researchers Patients Staff Resources to Position People: Board of Directors, CEO, COO, CSO, Executive Director, Associate Director of Operations and staff, Staff Directors, and outsourced personnel. Manage the annual operating budget of $12 million. POSITION REQUIREMENTS · Medical degree (MD), or PharmD/PhD. · Oncology experience a plus. · Experience in pharmaceutical drug development. · Ability to build collaborations among key opinion leaders, national organizations, pharmaceutical and biotechnology organizations Contact: Bob Weinstein The Carolan Group Email RESUME/CV to LWEINST650@gmail.com ]]>

<![CDATA[Job Title: EHS Specialist Job Description: Regeneron is a biopharmaceutical Company that discovers, develops, and commercializes therapeutic medicines for the treatment of serious medical conditions. Regeneron currently markets ARCALYST (rilonacept) Injection for subcutaneous use for the treatment of a rare, inherited, inflammatory condition. The company has therapeutic candidates in clinical trials for the potential treatment of cancer, eye diseases and inflammatory diseases, and has preclinical programs in other diseases and disorders. With a strong research base and product focus, Regeneron is able to understand thoroughly the biology of specific disease states, discover potential therapeutic candidates and evaluate product candidates in clinical trials. Regeneron has developed several proprietary platform technologies, which it has incorporated into a comprehensive system that allows it to accelerate the discovery and design of fully human antibodies and move these candidates rapidly into clinical development. Under the direction of the Sr. EHS Specialist assists in implementing various health and safety programs including Hazard Communication, Laboratory Safety, Radiation Safety and Infection Control Programs. Additional duties include waste disposal, safety equipment inspections, industrial hygiene surveys and assisting with environmental management. Excellent written and verbal communication skills are essential. This position requires 40 hours per week. Essential Functions of the Job: - Assists in implementing various environmental health and safety programs and initiatives under the direction of the Senior Environmental Health and Safety Specialist. - Assists in implementing environmental and safety management systems. - Implements emergency response programs. - Conducts routine surveys of laboratory and waste areas where low level radioactive materials are used. - Assists in developing EHS training content for online, on the job training and class room training sessions and performs training as necessary. - Responsible for inspection, collection, storage and disposal of biohazardous, chemical and radioactive waste. Waste minimization and assurance of proper disposal practices are one of the top priorities. - Performs ergonomic assessments and makes recommendations. - Performs Industrial Hygiene monitoring of laboratory and support personnel to interpret data and determine potential exposure to hazardous chemicals. - Performs EHS inspections of labs, support areas and offices. - Writes clear and concise safety related communications, including e-mails, letters, policies and procedures as required. Other Duties and Responsibilities: - Assist Facilities in projects as necessary. - Occasional requirement to work overtime. Experience: - Bachelors Degree - 1-3 Years of Experience - Excellent written and verbal communications skills. Computer literate. Ability to learn specialized software applications. Ability to develop and conduct EHS training sessions. EMT certification is a plus. Required Special Equipment and/or Programs: - Ability to use a PC, specialized safety and industrial hygiene equipment, various specialized applications such as Facilities Help Desk. We offer an extremely competitive compensation and benefits package including stock incentives, 401k with company match as well as the expected health and welfare benefits. Comprehensive relocation benefits are available, as required. EOE/M/F/D/V To apply, please submit your profile and resume at www.regeneron.jobs – Job Req # 2436 for immediate review and consideration.]]>

<![CDATA[If you are looking to Work Green and for Jobs in Green Industries, look no further than <a href="http://www.work-green.net" rel="nofollow">http://www.work-green.net</a>. At <a href="http://www.work-green.net" rel="nofollow">http://www.work-green.net</a> we see beyond simply "jobs" and offer the largest selection of filtered listings in the world as well as essential support, guidance and opportunities for your living, growing career at • Environmental and ecological non-profits • Laboratories • Alternative energy companies • Internships and fellowships • Educational institutions • Freelance assignments • Multi-disciplinary organizations as well as businesses related to green industries At only $9.95 a month, it is a great investment at any stage of a career in the Green, from entry level, mid-career, to senior/executive level. Check it out: <a href="http://www.work-green.net" rel="nofollow">http://www.work-green.net</a> ]]>

<![CDATA[A startup company needs a Chemist Consultant with experience in formulating lotions, scents, skincare and dermatology products. Please send resume. ]]>

<![CDATA[PharmaLegacy Laboratories Shanghai, China PharmaLegacy Laboratories is a preclinical Contract Research Organization (CRO) providing specialty services of pharmacology research in Bone/Orthopedics, Inflammation and Immune Diseases, Oncology, Liver Diseases and Hematological Diseases. With a vision to collaborate with our global clients for accelerating their mission to develop new therapies, PharmaLegacy provides quality services with productivity and timeline driven operations for drug R&D innovations. Located in Zhangjiang High Tech Industrial Park, Shanghai, PharmaLegacy seeks self-motivated Sales/Senior Sales Managers to join this exciting venture. In addition to a competitive compensation, the successful candidate will have the opportunity to thrive in the challenging and thrilling development of China’s biotech industry in the global setting. The primary responsibility of the selected candidates is to sell all the services of the company to a wide range of new and existing customers across the pharmaceutical and biotech industry in the USA. The role requires a strong emphasis on sales and organizational skills, as well as an overall technical proficiency in order to represent the company in all its service lines. The role will be responsible and accountable for meeting and, where possible, exceeding individual, team and company annual targets. The selected candidate will have to work well on their own as well as in a team environment. Specific Responsibilities • To develop business and relationships with new and existing customers, selling pharmacology research services applicable to the Pharmaceutical/biotech R&D organizations. • To identify, prioritize and qualify new customers and leads by developing business intelligence, understanding the customer base and exploring the market. • To keep in regular contact with prospect/client base; arranging appropriate face to face meetings or teleconferences and facilitating the use of scientific staff to gain business. • To ensure Sales Activity metrics are in line with set objectives. • To represent the company at conferences and trade exhibitions, ensuring timely and effective follow up to all leads generated and composing conference summary and feedback reports. • To develop strong relationships with external as well as internal customers. • To review all inquiries and follow up on all quotations, proposals and inquiries. • To promote customer service improvements and follow up on post sales feedback. • To participate in telephone campaigns and follow up on specific mailings targeted at new or existing product lines. Qualifications: • Successful track record selling services to the Life Sciences market, • Demonstrated ability to develop new market opportunities. • Bachelor’s Degree or above in a Life Science discipline. • Demonstrated influencing and negotiating ability. • Strong ethics and beliefs in the mission of developing new therapies. • Self-motivated starter with enthusiastic drive and ambition. • Possess outstanding communication skills, a strategic mindset, an ability to interface at an executive level and a polished presence in public presentation. ]]>

<![CDATA[A well-established tutoring group is looking for SAT tutors and Science tutors. Applicant must have a) a stellar educational background b) strong standardized test scores c) excellent communication skills d) amiability, maturity, patience, and a sense of humor Teaching/Tutoring experience is not required. Company will provide training. Please email resume with a cover letter. ]]>

<![CDATA[Envoy Medical Corporation Envoy Medical Corporation was founded in 1996 to design, develop and market implantable devices for the treatment of sensory hearing disorders. Envoy is a privately held organization with Corporate Headquarters in Minnesota. We have divisions established in Germany, France and Italy. Our mission is to improve the quality of life for millions of individuals suffering from sensorineural hearing loss. Over 21.5 million adults in the United States suffer from this condition. At Envoy, we’re changing the face of hearing loss by continuing to invent future generations of technology that restore hearing. Field Clinical Specialist – Position Summary: The Field Clinical Specialist is the “face of Envoy” with patients, surgeons, and clinicians. This career is multi-faceted in technical contribution paired with customer interaction. Responsibilities: • The Envoy Field Clinical Specialist works to enforce that the proper surgical technique is utilized for the implantation of Esteem® – The Hearing Implant. This prosthetic implantable device is the first medical solution for sensorineural hearing loss. • The FCE primary role is working with Esteem Implant Centers throughout the country to assure superior clinical outcome during surgical implantation. Working with surgeons can be challenging and rewarding on many levels, as anatomies and patients are unique. • Unyielding protocol enforcement is paramount with surgeons to ensure optimum results. • Managing recipient and clinician demands and expectations can be challenging, yet an important part of this role. • Ability to train small groups of surgeons. • Long-term growth opportunities are available for those who wish to participate. • Extensive domestic travel is required. Qualification Requirements: • Technical/Engineering/Science Degree required • Experience in medical devices can be beneficial • Desire to work in a surgical operating room • Driven to succeed and self-motivated • Excellent verbal and written communication skills • Results oriented with a desire to work on a team • Good organizations skills with the ability to pay attention to detail]]>

<![CDATA[About Oyster Oyster.com, the first and only hotel research and shopping website, is expanding and we are looking for a senior software engineer to join our team. Financed by Bain Capital Ventures and led by an accomplished and experienced management team, Oyster.com is dedicated to providing the most comprehensive and objective hotel information combined with a world class shopping experience. Formed in March 2008, Oyster.com management includes Microsoft alumnus Eytan Seidman, formerly Director of Core Relevance on Live Search (now Bing.com) -- and two highly accomplished serial entrepreneurs, Ariel Charytan and Elie Seidman. Our engineering team includes members who architected and scaled Microsoft's search engine between 2003 and late 2007. They hold computer science degrees from Cornell University, University of Pennsylvania and Harvard. Senior Software Engineer As a senior software engineer, you will develop and maintain the web services that power Oyster.com. Responsibilities can range from architecting trip planning tools to expanding our hotel search engine. You will need an eye for customer friendly design along with the skill to scale features across millions of pageviews and thousands of users. Our technology stack contains custom tools, open source projects, and commercial software. You will work with Python, PostgreSQL, Nginx, Windows, CentOS, C++ and more. Oyster has been repeatedly praised by the best and brightest; The New York Times, Wall Street Journal, LA Times, Economist, USA Today, 37 Signals and many others: <a href="http://www.oyster.com/about/in-the-news/" rel="nofollow">http://www.oyster.com/about/in-the-news/</a>. We are especially proud of being called a “well executed site” by 37 Signals – some of the toughest critics in the business. Qualifications • Bachelor's Degree in Computer Science • 5+ years of professional software development experience, with a preference towards web development • No requirement for language experience. We largely use Python and C++. • Experience with relational databases • Must have unrestricted work authorization to work in the United States What We Offer Joining our team full-time brings genuinely unique benefits: • 30" monitors with the best computers money can buy • We believe that one excellent worker is far better than two adequate performers; as such, we pay well and reward star performers as stars • Medical, dental, and a 401(k) • Meaningful equity/stock options in a startup with a very bright future • Friendly coworkers who are the best in their respective fields • A seasoned and successful entrepreneurial leadership team that has already achieved great success and knows how to focus and get stuff done Interested? Please submit your resume to jobs@oyster.com with "Senior Software Engineer" in the subject.]]>

<![CDATA[King Industries, Inc. has been a pioneer in the development, manufacturing, and marketing of specialty chemical products as additives for use in the coatings and lubricant industries for over seven decades. We currently have an opportunity in the Technical Service Department of our Coatings Division for a degreed Chemist with a minimum of ten years relevant coatings experience and the ability to perform duties and achieve objectives with a minimum of supervision and to interact well with customers. Candidates must have extensive background in the formulation, testing, and application of high performance urethane and melamine cross linked coatings plus working knowledge in utilizing additives to optimize the performance of high solids and waterborne industrial coatings. Skills Required: • Technical expertise in formulating and testing of industrial coatings • Experience in waterborne / high solids/ radiation curable & specialty coating systems. • Excellent formulating skills & practical working knowledge of urethane systems (2K, 1K, hybrid) and melamine cross linked systems. • Thorough knowledge of industrial coatings, applications, performance requirements, formulations and test methods. • Excellent communication skills, written and verbal plus the ability to interface well with customers. • Ability to perform duties/achieve objectives with a minimum of supervision. Education and Experience Requirements: • Minimum B.S. in Chemistry or Chemical Engineering with 10+ years relevant coatings experience. • Advanced degree is an asset. Duties and Responsibilities: • Work closely with Technical Marketing Manager for to develop and implement a dynamic technical strategy to increase sales of coatings products. • Develop formulations and performance data needed to support the marketing of products for use in waterborne, high solids & specialty coatings and elastomeric applications. • Prepare coating formulations and test panels. • Evaluate and interpret test results and offer suggestions and recommendations • Prepare progress/final reports on a regular basis. • Handle customer requests for product information and offer specific product recommendations to help customers solve specific problems. • Make periodic visits to customers for technical service calls and formal presentations and to follow up on specific technical projects. • Maintain a working knowledge of King Industries’ additive technology for the coatings industry. We offer an excellent salary and benefits package and an opportunity for professional growth. If you are interested in becoming a valued member of our team, please forward your cover letter and resume above e-mail address. ]]>

<![CDATA[Research Technician (mathematics background), Departments of Genetics and Neuroscience, Albert Einstein College of Medicine As one of a few labs at the forefront of the emerging field of connectomics, we seek to understand how the wiring of a nervous system determines the behavior of an organism, and to understand how this wiring is specified in the genome. Our lab uses the nematode C. elegans as a model organism because of its stereotyped behavior, relatively small nervous system, and well-studied genome. We are looking to hire a technician with significant background in mathematics to assist in an interdisciplinary project between the genetics and neuroscience departments. The technician will work on two aspects of this project: 1. Our lab has recently completed the connectome of the tail of the male C. elegans. This involved a two-year long effort to map out every synaptic interaction between neurons in the ganglia of the tail. We are seeking a technician to aid in the statistical analysis of this network using recently developed tools from the fields of applied mathematics and complex network analysis. The technician should have the mathematical maturity to survey research papers in these fields, and enough programming experience to implement these tools in a computing environment such as MATLAB, R, Java, or Python. 2. Our lab is engaged in an ongoing project to map the connectome of the head of the male C. elegans. The research technician will operate an electron microscope to photograph sections of the C. elegans nervous system, and will use image processing tools to prepare these photographs for analysis. The technician will also be involved in preparing the database of neuronal connectivity by annotating the synapses and cells in these images using specially designed software. The technician will have an opportunity to coauthor publications and present his or her results at scientific meetings. The successful candidate will likely be an individual interested in pursuing a career in scientific or applied mathematical research. Requirements: • B.A. or B.S. in Biology, Chemistry, Physics, Mathematics, Engineering, Computer Science or a related discipline. Significant coursework in mathematics and experience in computer programming strongly preferred. • Experience in MATLAB programming preferred, though experience with another computing environment and willingness to teach oneself a new language are sufficient. • The individual should be able to work in an independent manner to develop the tools necessary for the job, should be self-motivated, and should be able to communicate the results of his/her work to other members of the research community at the Albert Einstein College of Medicine and other institutions. ]]>

<![CDATA[Dear Students/Recent graduates: Work for one of the World’s largest book publishers. We have an encyclopedia titled: “Encyclopedia of Energy" that is partially done, however, the editors need help because of unforeseen circumstances. We are looking for bright upper classman, Masters, or Ph.D. students majoring in science or engineering or recent graduates to work from home to solicit by email contributors for the “Energy Encyclopedia”. We are willing to pay $10.00 per hour for this work. You can also earn a $100 bonus if you sign 25 or more contributions in a 40 hour period. Please submit a resume to be considered for this position. ]]>

<![CDATA[Our company is conducting a research study for a new formulation of a plant based raw food diet supplement. We are looking to recruit 200 man and women in the city (midtown west); bring them to our office where they will be given product for 40 days and return at the end for an evaluation. The study is supervised by a physician. This is not a recruitment solicitation; I am actually looking for a coordinator for the study to help with: recruitment, questionnaire development, data collection, processing of volunteers, data entry (Survey Monkey, Google Surveys…) etc. Time commitment: a few days leading to the study, a few days (evening) at the beginning of the study which is repeated at the end of 40 days.]]>

<![CDATA[Seeking experienced postdoctoral fellow to work in a state-of-the-art physiology laboratory (includes intravital cellular imaging for intracellular Ca2+ and pH) that will focus on physiologic responses of fluid shear stress on renal tubular epithelial cells (ion transport, gene and protein expression). Ideal candidates will have earned their PhD in physiology, biomechanical engineering, molecular biology and/or a related field. Highly motivated candidates with a recent PhD, and with excellent oral and written communication skills are preferred. Successful applicants will benefit from a multidisciplinary and collaborative environment with excellent research facilities. The accepted candidate will be expected to present research findings at scientific meetings; he/she will have the opportunity to pursue funding in related areas. To apply, please send a letter of application (summarizing research interests and career goals), curriculum vitae, and the names and contact information (e-mail addresses and phone numbers) of three references. Job Qualifications: PhD or MD/PhD are eligible Must be willing to work with animals ]]>

<![CDATA[Technical Sales Rep, Toxikon Corporation Toxikon Corporation, originally founded in 1977, is a Contract Research and testing company with laboratories in Bedford, MA and Belgium. Our mission continues to focus on providing quality services, competitively priced, with on-time delivery for the Pharmaceutical, Medical Device and Biotech industries. Toxikon is seeking an experienced outside sale person with successful selling skills. As a Technical Sales Representative, the appropriate candidate will provide Toxikon's testing services to assigned territories. We are seeking a self-starter with good presentation and communication skills. This individual will spend time learning about Toxikon, our services, and systems; identify, analyze, contact, and provide testing services to new customers, and; generate leads, prepare quotes, request protocols, and work with customer service and laboratory staff. The successful candidate will have a B.A., B.S, in life sciences or a strong understanding of life science testing and service industry and two to three years' sales experience. This position requires a strong understanding of the testing and service industry, including regulatory agencies, as well as the ability to converse with clients on testing & service needs (for pharmaceutical and medical device companies); prior CRO and/or lab experience preferred; experience with cold calls and client development required; proven ability to generate new accounts and account revenues of $5-10 million; must be self-motivated and a strong team player; excellent communication, presentation, organizational, and computer skills required, and; the ability to handle several projects concurrently is necessary. Solid computer skills, excellent organizational skills, and the ability to handle several projects concurrently are necessary. For additional information about Toxikon, please view our website at www.toxikon.com Submit resumes to: Human Resources Toxikon Corporation 15 Wiggins Avenue Bedford, MA 01730 Fax: (781) 271-1137 Email: hr@toxikon.com Toxikon employs 160 people and offers a generous benefit program including health, dental, fsa, std, ltd, life insurance and matching 401K plan. Toxikon is an EOE. ]]>

<![CDATA[About Us Cepheid (Nasdaq: CPHD), is an on-demand molecular diagnostics company that develops, manufactures, and markets fully-integrated systems and tests for genetic analysis in the clinical, industrial and biothreat markets. The Company's systems enable rapid, sophisticated genetic testing for organisms and genetic-based diseases by automating otherwise complex manual laboratory procedures. Cepheid's easy-to-use systems integrate a number of complicated and time-intensive steps, including sample preparation, DNA amplification and detection, which enable the analysis of complex biological samples in its proprietary test cartridges. Through its strong molecular biology capabilities, the Company is focusing on those applications where rapid molecular testing is particularly important, such as identifying infectious disease and cancer in the clinical market; food, agricultural, and environmental testing in the industrial market; and identifying bio-terrorism agents in the biothreat market. APPLY TO: <a href="http://www.cepheid.com" rel="nofollow">http://www.cepheid.com</a> OR Cepheid@agents.icims.com POSITION SUMMARY Successful candidate will be responsible for service support for our GeneXpert Product line, focusing on the Infinity. The job will offer a challenging role for a individual who enjoys the fast pace of a rapidly growing company that has cutting edge technology and market leadership in the Molecular Diagnostic market. RESPONSIBILITIES * Travel throughout North America and sometimes to Europe on short notice to support the company's products and field service partners. * Work on-call designated weekends to provide service support within a short period of time. * Partner with the Field Technical Service Support group to do installations (customer training). * Provide support of highly technical and/or sophisticated products. * Achieve and exceed Customer Satisfaction objectives * Perform routine standard procedures to isolate and fix problems in malfunctioning equipment or software. * Document and report the company's product "design reliability" and "maintenance issues" and/or problems to technical support. REQUIREMENTS * Bachelor's Degree in Electronics and/or Engineering * 5+ years experience in managing product development, lifecycle maintenance, sales support, and technical services * Capable of handling advanced complaints, troubleshooting skills, and knowledge of GMP & ISO requirements * Strong leadership skills with the ability to effectively supervise others' when needed * Possess the ability to work with customers and vendors at both a business & technical level * Exceptional time management skills * Ability to conduct presentations of technical information concerning specific projects or schedules * Experience with computer hardware and software * Be capable of interacting positively across all levels of the organization * Be capable of explaining technical procedures in writing or verbally * Able to multi-task and prioritize events and maintain composure under high levels of demand * Ability to work independently and be self - motivated * Able to travel about approximately 75% * Requires excellent systematic troubleshooting skills utilizing a structured and comprehensive process to determine the root cause and implement corrective action. * Requires excellent troubleshooting skills with automation robotics. * Ability to work independently with limited supervison * Proficient in reporting activities maintaining local spare parts inventory recording, travel expenses. PREFERRED QUALIFICATIONS Must be able to lift 45 lbs over the shoulder and place the equipment into a slot within a unit that is 5 feet high Abiltiy to maneuver/push equipment (weighing over 1,000 lbs) on wheels Ability to read target precisely (good vision) Cepheid administers its personnel policies and conducts its employment practices in a manner that treats each employee and applicant for employment on the basis of merit and experience, without regard to race, creed, color, national origin, sex (including pregnancy, childbirth, or related medical conditions), age, physical or mental disability, marital status, sexual orientation, citizenship status, ancestry, religion, gender identity, or any other protected characteristic as established by law.]]>

<![CDATA[Medical Technologist Position Description Cryos International – NY, a leading worldwide sperm bank, is seeking qualified part-time Medical Technologists. The Medical Technologist serves patients by providing precise and accurate Andrology and sperm bank laboratory results for the purpose of infertility assessment and management. This position is responsible for performing andrology laboratory services in accordance with the Laboratory Technical Procedure Manual. Available hours are dependent upon the availability of each part-time medical technologist. Responsibilities • Follow the laboratory’s procedures for specimen handling and processing, sperm test analyses; reporting and maintaining records of patient test results. • Maintain records that demonstrate that PT samples are tested in the same manner as patient specimens. • Adhere to laboratory’s quality control policies; document all quality control activities, instrument and procedural calibrations and maintenance performed. • Follow the laboratory’s established policies and procedures whenever test systems are not within the laboratory’s established accepted levels of performance. • Be capable of identifying problems that may adversely affect test performance or reporting of test results and either must correct the problems or immediately notify the general supervisor or laboratory director. • Participate in laboratory operations as directed. • Participate in laboratory proficiency testing programs. • Work cooperatively with the laboratory team and clients to provide good patient care and achieve the objectives and goals of the facility. Required Qualifications • Must hold a current Clinical Laboratory Technologist registration certificate through New York State. • Have a BS in chemical, physical, biological, or clinical laboratory science. • Must demonstrate an aptitude for performance of laboratory services. • Have proven skills to assess, input and retrieve information via computer systems. • Ability to work in a fast pace environment. • Ability to communicate accurately and concisely, and have extreme attention to detail. • Excellent interpersonal skills. Application Process • All applicants must hold a current New York State Clinical Laboratory Technician or Technologist license. • Please email a cover letter and resume to ny@cryosinternational.com. Do not include any attachments in the email. Please cut and paste your resume into the body of the email. ATTACHMENTS WILL NOT BE OPENED AND YOUR WILL DISQUALIFY YOU FOR EMPLOYMENT CONSIDERATION.]]>