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<![CDATA[Brown and Caldwell, a nationally recognized environmental engineering and consulting firm, has an exciting opportunity for a Client Service Manager (Managing Geologist, Engineer or Scientist) in our Houston, TX office. The CSM will be a recognized environmental services industry leader in the Houston area, with existing refinery, petrochemical, and/or chemical client relationships. With over 1,400 employees in 45 offices nationwide, Brown and Caldwell has been providing municipalities, private businesses and government agencies with sustainable environmental solutions for more than 60 years. We offer a collaborative environment with opportunities for growth and advancement in all professional disciplines. Responsibilities: The Client Service Manager is responsible to ensure exceptional client service, drive sales, and manage multi-disciplinary resources to deliver service and products across multiple projects. The person in this role provides high-level environmental consulting services for the petrochemical industry and related industries. Those services may include (but are not limited to): • Regulatory analysis and permitting • Site investigations • Application of remediation technologies • Environmental monitoring • TRRP and site closures • Reporting The Client Service Manager will develop existing and new relationships with key clients in the Houston marketplace, cultivating an exceptionally strong local/regional client base and/or national clients at multiple sites. Qualifications: • At least 10 to 15 years in environmental services consulting, working for and providing services to chemical/petrochemical companies; exploration and production companies, oil field service companies, or manufacturing companies • Technically proficient in the services provided • Recognition as a market leader, with considerable knowledge of sales and service opportunities in Houston and the gulf region; clients may have geographic distribution throughout the US • BS in geology, engineering or science preferred; professional registration in Texas is a plus • Ability to travel to client sites across the region and nationally as required. To apply, please click on the following link and fill out a brief application. <a href="http://tbe.taleo.net/NA9/ats/careers/requisition.jsp?org=BROWNCALDWELL&cws=1&rid=439" rel="nofollow">http://tbe.taleo.net/NA9/ats/careers/requisition.jsp?org=BROWNCALDWELL&cws=1&rid=439</a> Or, visit us at www.brownandcaldwell.com and click on Join Us. Brown and Caldwell values workforce diversity. EOE/AA]]>

<![CDATA[Please disregard previous ad. A position has become available for a Laboratory Technician in the Department of Pharmacology, at Baylor College of Medicine in Houston. The focus of our work is on structural and biochemical characterization of Serine/Threonine protein kinases. You will be involved in the complete process of the project, focusing on mass production of novel protein kinases and optimizing protein crystals, solving the structure of proteins, as well as biochemically characterizing them. The ideal applicant will have a BS/MS in a biological science, or the equivalent in professional qualifications and experience, and should have experience in molecular cloning, protein purification and x-ray crystallography. The laboratory is located in Texas Medical Center campus which provides an excellent environment for academia and research. The lab is well-equipped including robotics to facilitate overproduction and crystallization of proteins and has access to the Berkeley ALS beamline in the framework of the molecular biology consortium. Interested candidates should send three references and a resume to the email address posted above. ]]>

<![CDATA[A position has become available for a Post-doctoral Research Fellow in the Department of Pharmacology, at Baylor College of Medicine in Houston. The focus of our work is on structural and biochemical characterization of Serine/Threonine protein kinases. The successful candidate will be involved in the complete process of the project, solving the structure of proteins, as well as biochemically characterizing them. The ideal applicant will have a PhD in a biological science, or the equivalent in professional qualifications and experience, and must have experience in molecular cloning, protein purification and x-ray crystallography. The laboratory is located in Texas Medical Center campus which provides an excellent environment for academia and research. The lab is well-equipped including robotics to facilitate overproduction and crystallization of proteins and has access to the Berkeley ALS beamline in the framework of the molecular biology consortium. Interested candidates must send three references and a resume to the email address posted above.]]>

<![CDATA[Looking for an Energetic Polymer Chemist in the Houston area. Please submit your resume if you meet the following criteria: BS in Chemistry or Polymer related field of study At least 2-3 years of industrial experience. Must have strong interpersonal skills. Be willing to travel regularly. ]]>

<![CDATA[Houston Community College has openings in their SCIENCE DEPARTMENT for adjunct faculty (part time). Chemistry Professors should have a Masters in Chemistry and Physics Professors should have a Masters degree with 18 hours in Physics. If you would like to be a part of the HCC Science Department contact: Dr. Gholam Pahlavan at gholam.pahlavan@hccs.edu or call 713-718-7773]]>

<![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[<h2> Project Engineer ‘15’ (Houston)– 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[ Liquid Environmental Solutions (LES), the nation's leading exclusively Non-Hazardous Liquid Waste company is looking for Laboratory technican in the Houston Texas market. POSITION DESCRIPTION/SUMMARY: Under the general direction of the laboratory manager, the laboratory technician is responsible for performing analysis on all incoming samples for compliance with all site-specific, local, state and federal regulations for waste acceptance. ESSENTIAL DUTIES AND RESPONSIBILITIES: 1. Performs wet bench chemistry to analyze waste acceptance of samples and loads prior to disposal at facility. 2. Manages regulatory paperwork (manifests, bills of lading, logbooks, etc.) in accordance with local, state, and federal regulations for proper recordkeeping. 3. Serves as a technical liaison between customers and other departments of the facility. 4. Coordinates with the laboratory manager on other projects as needed. MINIMUM QUALIFICATIONS: 1. Three hours of college chemistry (wastewater experience may be substituted) 2. Basic knowledge of laboratory personal protective equipment (PPE) and safety 3. Basic computer skills (data entry, Microsoft Office) 4. Professional appearance and demeanor LES offers a full line of benefits to include; * Medical and dental options after 60 days * Life insurance * Short and long term disability insurance * All team members are provide stock options after completing 90 days * Paid Time Off Must be able to work day and afternoon shifts ]]>

<![CDATA[Pharm-Olam International, a multi-national clinical Contract Research Organization has an immediate opening for an experienced Clinical Trials Associate (CTA). This is a full-time, office-based position at our global headquarters in Houston. The CTA will act as the primary contact for the project team administration and to provide the Project Manager and all other project team members with advice, assistant and support as required, thus ensuring that the clinical trial is conducted in accordance with international regulatory and ethical guidelines for Good Clinical Practice, and assist the study team with the day-to-day conduct of international clinical studies with guidance as required. Additional Responsibilities 1. Assist the Project Manager, CRAs with the day-to-day administration of international clinical studies 1.1 Provide functional assistance to project team members with administrative, logistical and practical issues, including collection, distribution and filing of study documentation. 1.2 Track critical documents and inform the Project Manager of documents that are outstanding. 1.3 Notify the Project Manager when file notes are required to record missing documents in the Trial Master File 1.4 Request additional administrative resource if required and authorised by line manager. 1.5 Follow-up study team requests for clarifications; supplementary information; distribution of newsletters; updated contact details; and distribution of revisions of protocols and Clinical Investigator Brochures. 1.6 Assist Project Manager with generation of study specific forms for Investigator Site files. 1.7 Assist CRAs, Project Managers with collation of documentation required for submission to Regulatory Authorities and Ethical Committees. 1.8 Regularly review the status of key documentation in the Trial Master Files for compliance with SOPs to facilitate satisfactory audit inspections. 1.9 Scan critical documents onto CTMS and update project status as required by the study team. Working relationships « Reports to Clinical Trials Associate Manager « Collaborate with project teams and all POI staff « Communicate with Sponsor and sub-contractors if requested by Project Manager Education Requirements and Qualifications « Relevant CTA experience « Appropriate IT skills as required to perform duties « Reads and understands Pharm-Olam SOPs « Good written and verbal communication skills « Good attention to detail « Experience in managing workloads and timelines For immediate and confidential consideration, please forward resume and salary requirements by email or fax to +832 202 0564. This position is not eligible for relocation assistance. PRINCIPALS ONLY, NO PHONE CALLS PLEASE.]]>

<![CDATA[Position: Research Associate – Enhanced Oil Recovery Qualifications: • Geology, Petroleum Engineering, Chemical Engineering, or Microbiology Degree • B.S. with 2-5 years experience • M.S. with 1-2 years experience working in an industrial laboratory setting. • Previous core flood or enhanced oil recovery experience a plus. • Experimental design and set up experience desired. • Attention to experimental detail a must. Job Description: • Execute Core Flood experiments to test efficiency of Biotechnology Enhanced Oil Recovery (BEOR) products developed in the laboratory. • Generate data from core floods and input in existing spreadsheets. • Maintain core laboratory in operable condition. • Write and execute protocols, methods and SOPs • Exhibit good fundamental laboratory skills • Set up, operate, and maintain laboratory instruments. • Develop innovative methods for improvement of existing processes and equipment. • Strong academic and / or practical background in the design, analysis and evaluation of experiments. Overview of Company: Glori Oil has the world’s largest repository of subsurface producing reservoir specific microorganism samples from existing oilfields. We concentrate our efforts on the areas of microbial science and technology that will generate repeatable results to our customers and the long-term potential of the international energy industry. Glori Oil focuses its proprietary, environmentally safe BEOR™ technology on wells; designing customized microbe and nutrient treatment systems that increase oil production and extend the life of mature oil fields. Our mission is delivering state of the art bio-technology solutions to improve and increase recovery from mature oil wells and to solve complex problems associated with the production of oil, gas and water. • Please email resumes ]]>

<![CDATA[We are a rapidly growing biotech company in Austin, TX looking for a highly motivated Research Associate who will support and assist senior scientists with ongoing research and development. Successful candidates should have experience in performing RT-PCR, primer design, gel electrophoresis, western blotting, cloning, protein expression and purification. Experience with sequencing is highly desirable. Required Education and Experience: B.S. or M.S. in a Biological Science Related Field (Biochemistry, Molecular Biology, Microbiology, Pharmacology, Physiology) and industry/laboratory work experience. Candidate must be willing to move to Austin, TX. US Citizens and Permanent Residents only Email your CV and cover letter to apply for the position.]]>

<![CDATA[Reports to: President/CEO. Responsibilities: This position identifies and develops new technical and scientific projects that meet strategic company objectives Evaluates research, establishes collaborative R&D relationships to identify and pursue funding for advanced development or applications for company core technologies. Authors relevant scholarly articles for publication in peer reviewed technical or scientific journals Manages or serves as a scientific resource on a project team for sponsored research programs. Other duties as assigned. Experience/Qualification Requirements: The position requires a professional at the PhD level in chemistry, pharmaceutical sciences, medicinal chemistry, biomechanical engineering or related field, with a minimum of 10 years experience in conducting relevant research and development programs. A successful track record in writing and winning grant proposals for advanced research program solicitations by federal agencies including HHS/BARDA, NIH, NIAID, DoD, DTRA, TMTI. This position requires demonstrable experience to successfully identify and develop joint research and development projects that integrate the Company’s technologies with new biologics or chemical pharmacological entities. A minimum of 5+ years prior experience producing high quality written scientific documents for funding applications and publication, including writing, editing, and proofreading grant proposals, scientific manuscripts for peer review, white papers, protocols, and other scientific documents; searches for new funding opportunities; assists with updating reference materials. Assist with maintenance of databases and/or reference libraries. Search the internet and other sources for foundation and government grant opportunities. Translate scientific abstracts into lay terms. In addition, the position requires extensive demonstrated experience in the publication of scientific and technical papers in technical and peer-reviewed scientific journals, and experience in the presentation of such papers at national and international technical and scientific meetings. 5+ years of prior experience in project management of federally funded R&D programs with direct experience complying with federal reporting requirements. Software Requirements: The selected candidate must be computer-literate and be capable of generating technical email correspondence to scientific and senior level people in other organizations and be knowledgeable and proficient in Microsoft Office programs including MS Word, Excel, Powerpoint and other MS and non-MS software programs required for scientific assignments and professional management. ]]>

<![CDATA[VGXI, Inc. is a leading manufacturer of DNA plasmids. We deliver flexibility, experience, reliability and value to our clients’ challenging programs. We have an outstanding track record of success in manufacturing plasmid products under cGMP conditions for client companies, as well as supplying clinical products for studies in the U.S. and Europe. We are seeking a Validation Manager to join our team. <center>Validation Manager</center> The Validation Manager supports process validation activities at the plant and inter-plant levels to ensure regulatory compliance and effectiveness of facilities, equipment and processes. Responsibilities: • Provide technical expertise and guidance to plant manufacturing on the subject of process validation • Understand, implement and utilize risk-based validation system; provide input for ongoing improvements to the system • Support continuous improvement for the validation program to ensure efficiency, effectiveness and compliance; initiate corrective action as necessary • Execute activities as specified in Validation Master Plans and project plans and maintain project schedules • Lead manufacturing process validations, test method validations, process capability studies and process improvements • Select and utilize a wide range of appropriate statistical methodologies and techniques • Ensure that quality system inputs to the validation system are adequately addressed at the plant level; these inputs include undesirable trends or incidents of customer complaints, non-conforming materials and vendor quality problems • Participate in formal supplier quality evaluations; conduct supplier and internal quality audits relative to process control and process validation as requested • Perform test method validation activities including equipment parameter studies and gauge repeatability and reproducibility studies • Coordinate facility and maintenance activities to facilitate improvements and repairs impacting validation activities • Review and modify quality system documentation (as appropriate) related to validation activities to ensure compliance and effectiveness • Respond to questions related to validation activities during FDA and customer audits • Adhere to and ensure the compliance of all company policies, rules and procedures • Coordinate metrology program • Other duties may be assigned Required Qualifications: • Bachelor’s degree in a technical, engineering or science discipline; advanced degree preferred in engineering, science and/or business administration • Minimum of 3 years experience in hands-on process validation commensurate with the responsibilities outlined above Preferred Qualifications: • Strong process and statistical background • Knowledge of sampling plans, inspection criteria and techniques, critical attributes, process validations, statistical methods, disposition of non-conforming product, trending methods and environmental monitoring • Knowledge and experience with statistical process control, defects-per-million and other process monitoring methods and techniques • Strong communication, organizational and time-management skills • Ability to write clear and concise technical reports To Apply: Candidates seeking a challenging new opportunity are encouraged to submit their resume and salary requirements. EOE ]]>

<![CDATA[Quality Assurance Technician - Food Manufacturing JOB DESCRIPTION: A leading manufacturer of Egg Rolls and Asian entrees in the US, located in Southeast Houston is hiring a Quality Assurance Technician. Requires experience with quality control, inspection, and document review in a manufacturing facility. Must have high school diploma. Requires excellent reading, writing, and analytical skills, and basic computer and math skills. Must be detail oriented, attentive, and assertive and have excellent time management skills. DUTIES: Perform Pre-Op and Operational Sanitation Inspections. Perform packaging, manufacturing, and facility inspections on a daily basis. Develop, Implement and Monitor manufacturing procedures and SOP's for better efficiency. Check that HACCP and regulatory requirements and documentation are met and accurate. Perform quality evaluations and make recommendations for improvements. Collect and perform microbiological, chemical, physical analysis on samples. Perform instrument calibrations. Receive and approve incoming materials and ingredients. Assure the production personnel are complying with SSOP, SOP and GMP standards. JOB REQUIREMENTS: The basic requirements are education and/or experience in Microbiology, Biology, Chemistry, Biochemistry, Food Technology or related fields. Experience may be substituted for education depending on the nature of the experience, which should include some knowledge of microbiology bench work. USDA plant operations, Quality Assurance programs, and knowledge of HACCP Programs are required. Bi-lingual (English / Spanish) a plus. The successful applicant must be available to work either the 5am - 3pm or 2:30 - 1am shift depending on schedule - Monday-Friday. Some overtime and weekend work may be required. Contact Greg Birdsell through Craigslist with a resume if interested. ]]>

<![CDATA[Research Associate We are seeking a highly-motivated individual to fill a full-time Research Associate position at The Methodist Hospital Research Institute in Houston, TX. Responsibilities • Assist in research on new technologies and novel approaches for studying various virulence factors involved in the pathogenesis of microorganisms • Perform standard molecular and microbiological assays to characterize the role of various virulence factors. Experience The ideal candidate must have a BS/MS in Biology, microbiology, biochemistry or a related discipline, and possess academic or industrial research experience is optional. Experience in DNA extraction, gel electrophoresis, PCR, protein purification, and bacterial cell growth is desired. ]]>

<![CDATA[Leader in Environmental Consulting Services for the Oil & Gas Industry seeks Air Quality Specialist Seek the opportunity for upward mobility in a long established company, manage existing accounts and grow market share dramatically. To qualify for an interview you must show that you are exceptional in these areas: • BS or MS in science or engineering. • Minimum of 3 years technical experience with air permitting and compliance. • Ability to work with clients and regulators, and develop relationships in a team environment, • Self motivated and proactive with a superior work ethic • Strong technical and regulatory knowledge of gas & oil or petrochemical industry. Must have great communication skills, people skills and an infectious positive attitude. If you know you’re the best candidate for this position and can prove it, send your resume to sswanson@ceg-group.com by 09/30/2010. Subject Line: Air Quality Specialist Position. Do not apply if you are looking for a job, we are only interested in those seeking a career. Location: The Woodlands/Houston, TX Compensation: Salary + Incentives + benefits Candidates only. Recruiters please don't contact this job poster. Please do not contact job poster about other services, products or commercial interests. ]]>

<![CDATA[Leader in Environmental Consulting Services for the Oil & Gas Industry Seeks Geospatial Analyst To qualify for an interview you must show that you are exceptional in these areas: • BS or MS in geography, GIS or related field • Minimum of 1 year experience using ESRI ArcGIS software • Ability to work with clients and develop relationships in a team environment • Highly motivated and proactive with a superior work ethic Must be creative and have a personal commitment to excellence. If you know you are the best candidate for this position, send your resume to sswanson@ceg-group.com by 09/30/2010. Subject Line: Geospatial Analyst. Do not apply if you are looking for a job, we are only interested in those seeking a career. Location: The Woodlands/Houston, TX Compensation: Salary + Incentives + Benefits Candidates only. Recruiters please do not contact this job poster. ]]>

<![CDATA[Leader in Environmental Consulting Services for the Oil & Gas Industry seeks Project Scientist Seek the opportunity for upward mobility in a long established company, manage existing accounts and can grow market share dramatically. To qualify for an interview you must show that you are exceptional in these areas: • BS or MS in science or engineering covering areas of geology, hydrogeology, environmental science, or soil science. • Minimum of 3 years technical experience in at least two of the following areas: environmental assessments, remediation, oil spill contingency planning, wetland delineation, permitting and compliance. • Ability to work with clients and regulators, and develop relationships in a team environment • Highly motivated and proactive with a superior work ethic • Technical and regulatory knowledge of gas & oil industry • Strong writing skills. Must have great communication skills, people skills and an infectious positive attitude. If you know you are the best candidate for this position and can prove it, send your resume to sswanson@ceg-group.com by 09/20/2010. Subject Line: Project Scientist Position. Do not apply if you are looking for a job, we are only interested in those seeking a career. Location: The Woodlands/Houston, TX Compensation: Salary + Incentives + Benefits Candidates only. Recruiters please do not contact this job poster. ]]>

<![CDATA[Leader in Environmental Consulting Services for the Oil & Gas Industry seeks Project Manager Seek the opportunity for upward mobility in a long established company, manage existing accounts and can grow market share dramatically. To qualify for an interview you must show that you are exceptional in these areas: • BS or MS in science or engineering covering areas of geology, hydrogeology, environmental science, or soil science. • Minimum of 3 years technical experience in at least two of the following areas: environmental assessments, remediation, oil spill contingency planning, wetland delineation, permitting and compliance. • Ability to work with clients and regulators, and develop relationships in a team environment • Highly motivated and proactive with a superior work ethic • Technical and regulatory knowledge of gas & oil industry • Strong writing skills. Must have great communication skills, people skills and an infectious positive attitude. If you know you are the best candidate for this position and can prove it, send your resume to sswanson@ceg-group.com by 09/20/2010. Subject Line: Project Manager Position. Do not apply if you are looking for a job, we are only interested in those seeking a career. Location: The Woodlands/Houston, TX Compensation: Salary + Incentives + Benefits Candidates only. Recruiters please do not contact this job poster. ]]>

<![CDATA[Leader in Environmental Consulting Services for the Oil & Gas Industry seeks Senior Project Manager Seek the opportunity for upward mobility in a long established company, manage existing accounts and projects. To qualify for an interview you must show that you are exceptional in these areas: • BS or MS in geology, hydrogeology, soil science, environmental science or engineering and has obtained a PG or PE or can obtain a PG or PE within 1 years time. • Minimum of 6 years technical experience in at following areas: environmental assessments, remediation, sub-surface remediation systems, and groundwater modeling. • Ability to work with clients and regulators, and develop relationships in a team environment • Highly motivated and proactive with a superior work ethic • Technical and regulatory knowledge of gas & oil industry • Strong writing skills. Must have great communication skills, people skills and a positive attitude. If you know you are the best candidate for this position and can prove it, send your resume to sswanson@ceg-group.com by 09/20/2010. Subject Line: Senior PM Position. Do not apply if you are looking for a job, we are only interested in those seeking a career. Location: The Woodlands/Houston, TX Compensation: Salary + Incentives + Benefits Candidates only. Recruiters please do not contact this job poster. ]]>

<![CDATA[Leader in Environmental Consulting Services for the Oil & Gas Industry Seeks Senior Project Manager Are you seeking the opportunity for upward mobility in a long established company, managing existing accounts and projects? To qualify for an interview you must show that you are exceptional in these areas: • BS or MS in geology, hydrogeology, soil science, environmental science or engineering and has obtained a PG or PE or can obtain a PG or PE within 1 years time. • Minimum of 6 years technical experience in at following areas: environmental assessments, remediation, sub-surface remediation systems, and groundwater modeling. • Ability to work with clients and regulators, and develop relationships in a team environment • Highly motivated and proactive with a superior work ethic • Technical and regulatory knowledge of gas & oil industry • Strong writing skills. Must have great communication skills, people skills and a positive attitude. If you know you are the best candidate for this position and can prove it, send your resume to sswanson@ceg-group.com by 09/20/2010. Subject Line: Senior PM-R Position. Do not apply if you are looking for a job, we are only interested in those seeking a career. Location: The Woodlands/Houston, TX Compensation: Salary + Incentives + Benefits Candidates only. Recruiters please don't contact this job poster. ]]>

<![CDATA[Biomat USA, Inc., a part of the global Grifols family of companies, specializes in the collection of plasma for use in life-saving therapies. Biomat USA, Inc. , along with PlasmaCare, Inc., have a network of over 80 plasmapheresis donor centers throughout the United States. These state-of-the-art facilities collect plasma from donors and operate according to the highest standards of quality. For more information, please visit our website at <a href="http://biomatusa.grifols.com" rel="nofollow">http://biomatusa.grifols.com</a> Under the supervision of the Facility Manager and/or Operations Manager, you will be responsible for assisting with the daily management of operations of the donor center, supervising operations and quality control, and ensuring compliance with all applicable policies and regulations. ESSENTIAL DUTIES AND RESPONSIBILITIES include the following. Other duties may be assigned. Responsible for all aspects of the donor facility when the Facility Manager is not present. Perform any/all tasks within the plasma center; train production employees and demonstrate how tasks are to be performed to meet company standards, and on occasion, fulfill the role of production employees when the need arises. There will be many occasions when you will be the manager of the donor center, up to 40 hours/week or more. Create appropriate organizational environment and value systems which stimulate the morale and productivity of the work force and its leadership. Provide strategic direction, planning, and customer focus. Develop action plans to improve operations and supervise the implementation of improvements. You will be required to facilitate internal and external audits. Supervise donor selection, plasma collection, and all manufacturing records to maintain the highest production standards in accordance with Federal and State regulations, with FDA approved Standard Operating Procedure manual, OSHA, CLIA, and cGMP, through systems in place and via Quality Supervisor. Responsible for all personnel functions including hiring, development and training, disciplinary actions and termination, and maintenance of all personnel records. Determine adequacy of inventory of all goods and supplies necessary for center operation and oversee ordering goods as needed. Assure that subordinates maintain the facility in a neat and clean condition and all equipment is kept in good working order. Submit timely and accurate reports on a daily/weekly and monthly basis or when requested. Develop and implement active donor recruitment advertising campaign to improve production levels. Control center donor funds and ensure that all financial records are accurate and in order. Keep immediate superior informed of any irregularities within the center and provide action plans to improve and correct center deficiencies. Minimize center liability through constant risk management review. Signed Statement of Responsibility and Curriculum Vitae on file at the center and Authorized Official’s office. REQUIRED EDUCATIONAL QUALIFICATIONS To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable qualified individuals with disabilities to perform the essential functions. College Degree (unless waived by senior management of Biomat USA, Inc.). Evaluation and/or translation of any foreign education (high school, university, or professional training) must be provided. REQUIRED EXPERIENCE/SKILLS One (1) year plasma experience, including six months experience as an Operations Supervisor. Must have legible handwriting. Must be able to read, write, and speak English. Must be able to use a computer. PHYSICAL REQUIREMENTS: Ability to travel via automobile and/or airplane. Ability to stand for extended periods of time – up to four (4) hours at a time. Ability to view video display terminal less than 18” away from face – up to four (4) hours a time. Ability to lift, tug, pull up to fifty (50) pounds. Ability to handle mental stress. To Apply to this Position, please use the following link <a href="http://hostedjobs.openhire.com/epostings/submit.cfm?fuseaction=app.dspjob&company_id=16052&jobid=217868&jobboardid=632" rel="nofollow">http://hostedjobs.openhire.com/epostings/submit.cfm?fuseaction=app.dspjob&company_id=16052&jobid=217868&jobboardid=632</a> ]]>

<![CDATA[Company: Glori Oil Limited Location: South West Houston Research Associate Glori Oil Limited is seeking a highly-motivated individual to fill a full-time Research Associate position at its research facility in Houston, TX. Responsibilities • Assist in research on new technologies and novel approaches for studying microorganisms in petroleum reservoir environments. • Perform standard microbiological and molecular assays to characterize field samples. Experience The ideal candidate must have a BS/MS in microbiology, biochemistry or a related discipline, and possess 2 or more years of academic or industrial research experience. Experience in microfluidics, fluorescent microscopy, anaerobic cell cultivation, DNA extraction, gel electrophoresis, and PCR is desired. Overview of Company Glori Oil has the world’s largest repository of subsurface producing reservoir specific microorganism samples from existing oilfields. We concentrate our efforts on the areas of microbial science and technology that will generate repeatable results to our customers and the long-term potential of the international energy industry. Glori Oil focuses its proprietary, environmentally safe BEOR™ technology on wells; designing customized microbe and nutrient treatment systems that increase oil production and extend the life of mature oil fields. Our mission is delivering state of the art bio-technology solutions to improve and increase recovery from mature oil wells and to solve complex problems associated with the production of oil, gas and water. ]]>

<![CDATA[This is a blue-collar, hands-on position. Responsible for handling, treatment and disposal of hazardous chemicals. Excellent opportunity in the environmental industry. A degree in Chemistry/Biology/Environmental and knowledge in DOT regulations is beneficial. Company will train. Must have a drivers license to apply. Must pass a physical, drug screen, and background check. Email your resume or apply in person at NSSI, 5711 Etheridge street, Houston, TX, 77087. Monday - Friday from 8:30 - 3:00 pm.]]>

<![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 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[We have imideate opening for expirienced( min 2years) Wellsite Geologists and/or Mudloggers.Must be able to work in the office and field.Base salary+ field bonus]]>

<![CDATA[Petroleum Geologists wanted with college degree, for office and field work.Must be able to work and travel to the oil fields.Training will be provided. ]]>

<![CDATA[Immediate opening for a CERTIFIED, BILINGUAL, Lab Technician for a busy out-patient clinic. This position will perform ON-SITE PROCESSING of samples for varied testing, including HEMATOLOGY ANALYSIS. Must be familiar and have minimum of 6-months experience operating labratory equipment, including FAMILIARITY USING A CELL-DYNE MACHINE. This position will be working within a busy clinical environment where urgent care services have recently been added, We offer a fun, dynamic work environement with a fantastic team and flexible schedule. Position Responsibilities: • Assists with receiving, logging, and collecting specimens. Prepares specimens for technical testing. • Assists with identification and labeling of specimen. Stores and distributes specimens. • Performs laboratory testing as directed. • Files reports and laboratory requests. • Prepares labels for slides and stains slides. • Changes and prepares various solutions and stains. • Performs quality control checks of instruments, solutions and test results against established standards. Maintains quality assurance and proficiency testing as required by CLIA. • Performs venipuncture and capillary punctures on patients. Identifies and labels specimens. • Operates, cleans, and sterilizes laboratory equipment, glassware, and instruments. Cleans work area. • Answers telephone, takes messages and provides routine laboratory information. • Checks inventory of supplies and assists with placing orders. • Attends required meetings and participates in committees as requested. • Enhances professional growth and development through in-service meetings and educational programs. • Follows the Legacy guidelines related to the Health Insurance Portability and Accountability Act (HIPAA), designed to prevent or detect unauthorized disclosure of Protected Health Information (PHI). • Maintains strict confidentiality. • Maintains established Legacy policies, procedures, objectives, quality assurance, safety, environmental and infection control. • Implements job responsibilities in a manner that is consistent with the LEGACY Mission and Code of Ethics and supportive of Legacy’s cultural diversity objectives. • Supports and adheres to LEGACY Service Guarantee. • Performs other related work as required. Qualifications: • Certification Required: Certification as a laboratory assistant or medical assistant (or equivalent per state regulations). • Bilingual required: Fluent in both English/Spanish • Graduation from high school or GED. Fifteen college semester hours of courses in chemistry, biology, or related fields or six months of experience in medical laboratory. • Require minimum 6 months experience performing medical laboratory assistant duties. • Under the supervision of a licensed healthcare provider or laboratory director, performs medical laboratory tests and procedures of waived and Provider Preferred Microscopic Procedures (PPMP) in accordance with applicable guidelines. • Experience performing hematology analysis with CellDyne machine and other equipment for on-site sample processing. ]]>

<![CDATA[Strategic Account Manager Texas 28105 Position Description As a successful Strategic Account Manager, you will add to the growth of our company overall, by building value for our solutions and increasing revenues through renewable business relationships. You will be responsible for driving new business opportunities to support the strategic growth and expansion in a targeted marketplace. You will identify, develop and present product and service solutions that best meet our clients' strategic business needs. Utilizing effective consultative sales and servicing strategies, you will be responsible for managing and cultivating new business opportunities for the development of long-term business partnerships by creating superior value for our clients. Key Responsibilities • Effective penetration and expansion of specific vertical industry markets to create a strong client base • Leveraging resources and relationships to forge new consultative client business relationships • Conducting direct business-to-business sales, business-to-business cold calling, and phone based business-to-business prospecting resulting in successfully obtaining customer appointments. • Application of critical thinking, creativity and effective business communication skills to identify key client needs and formulate appropriate EBI solutions • Exercising effective consultative sales strategies and closing techniques to successfully achieve sales and performance goals monthly, quarterly, and annually Requirements • Minimum 4-5 years demonstrated successful experience with consultative sales and business development within the environmental consulting industry. • Demonstrated prior experience with pharmaceutical, biotechnology, and healthcare client markets • Expertise in one or more non-remediation based EH&S technical area • Ability to balance development of new business while maintaining existing client base • Strong negotiation skills; ability to drive decision-making • Strong collaboration skills; ability to facilitate service team approach to ensure customer satisfaction and follow-through • Capacity to apply critical thinking, creativity and effective business communication skills to identify critical client needs and formulate appropriate EBI solutions • Maintains a high profile externally and through membership/ attendance in industry and professional functions, continually increasing contact base • Unyielding drive to close high revenue and long-term business relationships • A creative, entrepreneurial spirit with a high level of business expertise and acumen • Strong knowledge of PC software programs, e.g., word processing, spreadsheets, database management, E-mail and Customer Relationship Management programs • Ability to work independently; effective time management skills, with strong organization and prioritization abilities Other Knowledge, Skills or Certifications Preferred • Recognizes relationship networks, stake holder influence and strategic value • Conducts formal presentations • Understands the competitive landscape in the local area • LEED certified • Understands "Green" influences and sustainability Educational Requirements • Bachelor's degree in Business or related field of study Company History EBI Consulting was founded in 1989 with the purpose of creating value for our clients in the health care, real estate, manufacturing, telecommunication and industrial sectors by utilizing innovative approaches to engineering, compliance, environmental and industrial hygiene services. EBI grew to $40 million in revenues in 2007 and is expected to exceed this in 2010. EBI Today Business Segments: 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 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. 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. EBI has been successful in providing many clients with quality Environmental, Health and Safety (“EHS”) consulting and engineering, at the same time ensuring all services and implemented programs would improve both the financial and organizational performance of that client. This is accomplished by utilizing EBI’s team of professionals who can effectively identify and address the client’s EHS concerns in a pro-active and cost-effective manner. As such, for the past 20 years, EBI’s principals, scientists and senior engineers have developed and delivered comprehensive EHS programs for many organizations on a local, regional and worldwide basis. We have a diverse client base traversing among life-sciences, healthcare, financial, manufacturing, real estate, educational, academia, telecommunication and other business sectors. There are many ways by which EBI has assisted its clients to develop, implement, improve or maintain successful EHS management programs. The following is a brief list of projects and/or services, which are provided by EBI: • Development of plant and corporate environmental health and safety plans, standards and guidelines; • Development of EHS management information systems, performance metrics and related reports; • Gathering EHS data for trend analysis and management reporting; • Review of EHS management systems, plans and programs and related gap analysis; • Conducting site investigations – including Phase-I and II assessments and site remediation; • Risk assessments of the facility and its operations for compliance to various OSHA, NFPA, and other regulations; • Implementation of programs to minimize risk such as Emergency Preparedness, chemical management, laboratory practices and waste management; • Establishing compliance calendars for the facility to track facility permits, training and other requirements; • Facilitating or participating in site committees (Safety, Bio-safety, process management, IACUC, etc.); • Incident/accident root cause analysis; • Customized training for EHS, DOT, SPCC, wastewater operations, etc.; 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 jobs@ebiconsulting.com. You must include the following information: 1. Reference job #, job title and resource 2. Brief summary of past related experience (highlight your experience as it relates to our need & industry); 3. List of your education credentials and professional registrations 4. Salary history We look forward to hearing from you! ]]>