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<![CDATA[ We have been retained by a food manufacturer with 20 plus years of presence in the U.S., to assist them in the recruitment of a Director Food Safety and Quality. A nationally known leader in their field, our client is focused on the development and supply of health nutrition products. These include dairy, bakery, confectionary, fruit beverage and food service markets. Quality assessment and management is a key performance indicator for the company, ensuring safe- high quality products to their customers. This will be a highly visible position within North American organization. The Director of Food Safety and Quality will report to the Vice President of Operations. QUALIFICATIONS: BS Degree in Food Science, Agriculture, Engineering, Biology/Chemistry or equivalent. Minimum of 10 years of quality/operational/technical experience with at least five years of progressive management experience in Quality Management. MS in Food Science, Biology/Chemistry preferred. Minimum three years of quality experience in the food, beverage, pharmaceutical and similar industries. Aseptic processing experience a plus. Fruit experience a plus. Must have been a Plant Quality Manager. Corporate Quality experience is a plus. Must have a strong background in SPC, continuous improvement and process management and control. Six Sigma and/or Total Quality experience a plus. Must have prior experience working with major customers. B2B background a plus. Market and Customer Orientation, ability to understand market and meet the needs of external and internal customers. Achievement Orientation, ability to make decisions, take responsibility for actions and able to handle crisis. Ability to travel 50%. Willingness to relocate to the MidWest.]]>

<![CDATA[ Helper for Research Group needed, telecommute possible for right individual. Specific details given so get back with us today. ]]>

<![CDATA[Regional Monitor Needed Site locations: Nationwide 100% committment (40 hrs) Must have 2 years+ experience as a monitor Must have at least 1 contract job and 1 perm job as a monitor Must have EDC experience Have to know if every monitor job was perm or contract on resume Top 5 CRO in world is looking to add a 100% available REGIONAL CONTRACT CLINICAL RESEARCH ASSOCIATE to their team. Description: Looking for experienced a Clinical Research Associate who will work regionally from home and be responsible for monitoring the progress of clinical trials at investigative sites, to ensure that they are conducted, recorded, and reported in accordance with the protocol, standard operating procedures, ICH-GCP, and all applicable regulatory requirements. This person will be completely accountable for the site management and data quality of each site for which they are responsible. They must be able to operate a home-based office and be fully functional as a home-based monitor. Travel will be upwards of 70%-80%. Minimum of 2 years as a regional CRA/Monitor. Resume must outline/explain relevant monitoring experience/skills. Strong attention to detail and Medical Terminology required. Ability to effectively communicate and complete accurate reports/forms, etc. Candidates MUST have at least a Bachelor's degree in Health Sciences or licensed or certified health care training (i.e. RN) or equivalent experience. ]]>

<![CDATA[Hatch Staffing Services is currently looking to fill Analytical Lab Chemist positions for our Client in both the Milwaukee and Port Washington areas. Job responsibilities include but are not limited to: <li>Conduct routine analytical testing and specialized analytical testing <li>Document all test results</li> <li>Learn all aspects of laboratory instruments</li> Requirements include but are not limited to: <li>5th year college certificate with strong emphasis on natural science</li> <li>Ability to read, analyze and interpret information</li> <li>Excellent communication skills</li> <li>Strong organizational and time-management skills</li> <li>Good computer skills and knowledge of Microsoft Office and Outlook, statistical analysis software and the Internet</li> <li>Strong mathematical concepts such as fractions, percentages, ratios and proportions</li> Apply today! For immediate consideration, attach your resume when applying to this posting. You may also email it directly to jenny@hatch.com - please include the job title in the subject line.]]>

<![CDATA[Working title: Research Specialist Official title: Associate Research Specialist or Research Specialist or Senior Research Specialist Degree and area of specialization: BA/BS required, or M.S. degrees desirable in biology, chemistry, physics, or computer science. Minimum number of years and type of relevant work experience: At least 1- 2 years work experience desirable. Must possess excellent communication skills, both written and oral, and be inclined to work as part of a team; should also possess a high-degree of self-motivation and initiative. Must have experience with bioinformatics software, a broad range of molecular biology techniques, and some experience in the genomic sciences. Strong organizational skills required. Proficiency in Linux and programming languages desirable. Principal duties: This individual will work under the direction of a project scientist for genome mapping activities within the Laboratory of Molecular and Computational Genomics. Responsibilities will include working directly with the scientist on the experimental and computational aspects of scientific projects and the preparation of technical scientific reports or grant materials for federal and nonfederal support agencies. The ideal candidate will be facile with performing both laboratory work and computational tasks involving common molecular biology, or genomics software. Work will center on the creative application of new genomic analysis technologies (based on novel single molecule effects) to bacterial, parasite, human, mouse, and crop genomes. Other responsibilities include facilitating the exchange of materials and data between collaborators. Required scientific background is varied to cover biology, chemistry, physics, and engineering, but core competence in the genomic science will be essential for daily research activities. More specifically duties will include: -Preparation of DNA samples for single molecule analysis; adaptation of standard techniques to novel samples. -Construction of “finished” genome maps/sequence, using laboratory computational tools and single molecule technologies. Follow-up work that includes standard molecular biology techniques—electrophoresis, PCR, cloning, etc. -Preparation of reports describing laboratory aspects of genome analysis performed. A one period of evaluation will be required. Number of positions open: 1 See PVL - <a href="http://www.ohr.wisc.edu/pvl/pv_060312.html" rel="nofollow">http://www.ohr.wisc.edu/pvl/pv_060312.html</a>]]>

<![CDATA[Aquatech International Corporation is seeking a chemist for analytical support work in their Applications, Development, and Testing department. This opening is in the Industrial Concentration and Desalination laboratory located in Hartland, Wisconsin. This position is in an industrial laboratory specializing in wastewater characterization for in-house engineering use and customer reports. The person hired will report to the Applications Development/Testing manager and will be responsible for all laboratory work from analyses to maintaining labware in a ready to use condition. This is not considered a short-term position. The qualified candidate should be committed to a long-term goal of staying and becoming a wastewater treatment specialist providing input to chemical/mechanical process engineers for equipment design and troubleshooting. Qualifications • BS degree in Chemistry, Inorganic Analytical Chemistry, or related field OR • Associate in Applied Science Degree with strong chemistry / science course work • Experience/training in bench top ‘wet’ chemistry analytical procedures • Experience/familiarity with standard laboratory instruments such as pH and conductivity meters, spectrophometers, centrifuges, analytical balances, and microscopes • Work precisely in solution making, with measuring devices, data handling and instrument operation • Demonstrate initiative and willingness to learn and grow in responsibility on the job • Communicate and receive precise chemical data and procedures • Understand and practice laboratory safety procedures • Understand and use material safety data sheets, etc. • Use software for instrument operation and data handling • Ability to work independently, with a minimum of supervision • Mechanical/technical background desired but not necessary Analyses performed per Standard Methods on various wastewaters • EDTA Titrimetric methods for Ca, Mg, hardness determination • Mercuric nitrate method for chloride • Molybdosilicate method for silica • Turbidmetric method for sulfate • Alkalinity analyses • Conductivity determination • Total solids, Total dissolved solids, and Suspended solids determination • Density measurements • Boiling point elevations • Constitution of precipitated solids • Others that are practical and of use for a small lab Additional duties • Perform bench top studies of customer supplied wastewaters to characterize performance when heated to boiling and concentrated to a Zero Liquid Discharge condition typical of mixed salt crystallization evaporators • Perform vacuum and pressure filtration on precipitated solids • Determine methods of dissolving any scale formed during the evaporation process • Determine crystal morphology of precipitated solids during zero liquid discharge testing using steromicroscopy • Perform corrosion testing of various metals in synthetic solutions and inspect afterwards for corrosion type and characterization • Prepare synthetic solutions to simulate customer wastewaters for preliminary characterization • Prepare technical reports for issue to the customer detailing the characteristics of their particular wastewater • Prepare in-housie engineering reports for use by equipment design engineers • Coordinate with outside labs for analyses that cannot be accomplished in-house • Prepare reagents for in-house analyses • Maintain reagent and lab inventory • Maintain calibration records for lab equipment • Maintain MSDS documentation • Maintain cleanliness of lab equipment including glassware used in lab analyses and testing Future Opportunities • Career advancement will involve pursuing a baccalaureate (minimum) or higher degree in chemistry (or related field) within 4 to 5 years • There is the potential that the selected candidate for this position may be promoted within 4 to 5 years Location: 1120 James Drive Suite B 105 Hartland, WI 53029 Hours: Typical working hours will be Monday – Friday 8:30AM – 5:00PM* Additional work hours, including evening and weekends maybe needed to meet business needs Start Date: November 2008* *Schedule and start date are items that can be discussed with qualified applicants To Apply Send your resume and cover letter, indicating salary requirement and possible start date to Erin Sheets sheetse@aquatech.com Please do not contact, mail, and/or call the facility directly. ]]>

<![CDATA[Seeking a degreed Hydrogeologist. Great company outstanding pay.]]>

<![CDATA[As a Production Scientist on our Maxwell Production Team you will be charged with creating kits, reagents and other materials for distribution to our customers. Individuals in this position are responsible maintaining instrument inventory, implementing new product offerings and manufacturing improvements, as well as creating a wide variety of components to meet production specifications. Successful candidates will have a solid understanding of the manufacturing process as well as working knowledge of a highly regulated environment such as IS013485 and cGMP. Mechanical aptitude is a plus. Preferred Qualifications: <ul><li>Minimum Bachelor’s degree in the life sciences discipline with 2 plus years of industrial experience in QC Testing and DNA/RNA Isolation.</li> <li>Well defined lab techniques including timing, speed and accuracy.</li><li>Attention to detail, written/verbal communication skills, organizational skills and ability to work independently and on multidisciplinary teams.</li> <li>Familiarity with molecular biology assay methods, contaminant testing, and product applications testing.</li> <li>Drive to be successful and thrive in our organization.</li> <li>Prior experience writing and maintaining standard operating procedures.</li></ul> Click here to apply: <a href="https://hostedjobs.openhire.com/epostings/jobs/submit.cfm?fuseaction=dspjob&id=23&jobid=189851&company_id=15945&version=2" rel="nofollow">https://hostedjobs.openhire.com/epostings/jobs/submit.cfm?fuseaction=dspjob&id=23&jobid=189851&company_id=15945&version=2</a> Repeatedly ranked as one of the top 10 places to work in the industry, Promega supports the strength and contribution of the individual. Promega understands that life is a balance of work, family and personal growth. Promega is proud to be an Affirmative Acton/Equal Opportunity Employer. ]]>

<![CDATA[As a Production Scientist on our Amplification team you will be charged with creating large-scale versions of our Genetic Identity and Forensic related products for distribution to our customers. Individuals in this position are responsible for leading custom orders through the production process, implementing new product offerings and manufacturing improvements, as well as creating a wide variety of components to meet production specifications. Successful candidates will have a solid understanding of the manufacturing process as well as working knowledge of a highly regulated environment such as IS013485 and cGMP. Preferred qualifications: <ul><li>Minimum Bachelor’s degree in a scientific discipline with 4 plus years of industrial experience in PCR, RT-PCR, and qPCR techniques.</li> <li>Well defined lab techniques including timing, speed and accuracy.</li> <li>Attention to detail, written/verbal communication skills, organizational skills and ability to work independently and on multidisciplinary teams.</li> <li>Familiarity with molecular biology assay methods, contaminant testing, and product applications testing. </li> <li>Drive to be successful and thrive in our organization.</li> <li>Prior experience writing and maintaining standard operating procedures.</li></ul> Click here to apply for this position: <a href="https://hostedjobs.openhire.com/epostings/jobs/submit.cfm?fuseaction=dspjob&id=23&jobid=189846&company_id=15945&version=2" rel="nofollow">https://hostedjobs.openhire.com/epostings/jobs/submit.cfm?fuseaction=dspjob&id=23&jobid=189846&company_id=15945&version=2</a> Repeatedly ranked as one of the top 10 places to work in the industry, Promega supports the strength and contribution of the individual. Promega understands that life is a balance of work, family and personal growth. Promega Corporation is an equal opportunity/affirmative action employer. ]]>

<![CDATA[Seeking a Superintendent for a local Meat company. This person must have experience and working knowledge of boilers and refrigeration at a industrial capacity level. Experience in the meat industry is preferred, but not required. This position will have supervisory direct reports. Degree is not required and experience is preferred. Please contact Jessica at the e-mail listed below with a copy of your Resume in a Word format if interested. Please state your salary requirements as this position is negotiable.]]>

<![CDATA[Quality Assurance Manager Our client is a growing contract manufacturer who is committed to being the leader in the contract manufacturing of disposable products. The product lines include Over The Counter drug products, topical ointments, aseptic wipes, and other consumer goods. Their platform for growth is based on exceeding customer expectations in product knowledge, quality, customer service, innovative research and development and ethical business practices. Currently, we are recruiting for qualified candidates for an opportunity to work with a growing organization as a Quality Assurance Manager. This is a direct-hire opportunity. Job Responsibilities The Quality Assurance Manager is responsible for managing the quality assurance program to the requirements of cGMPs and customer requirements. The QA Manager is responsible for insuring continuous production of products consistent with FDA standards. Essential Duties and Responsibilities: Develop and analyze statistical data Help to outline and define present standards and establish proposed quality standards of in-process and finished products Develop and maintains batch history review program Develop and maintain quality assurance objectives in line with company objectives and goals Create, implement, and maintain inspection criteria and procedures Investigate customer complaints, create and execute corrective action plans Applies total quality management Directs workers engaged in inspection and testing activities to ensure continuous control over material, facilities and products Interacts with vendors to insure quality of all purchased raw materials and equipment Creates and directs FDA acceptable validation programs Oversees quality assurance training programs Responsible for all audits from customers, third party auditors, and regulatory agencies Responsible for the internal audit program Job Requirements Qualified candidates should possess a minimum of a Bachelor’s Degree in Engineering or the Sciences. Candidates should possess a minimum of five years of experience in a quality assurance leadership role within an FDA regulated environment. Prior experience with items regulated by the CFR with regards to pharmaceutical products, topicals, and antiseptic wipes is highly desirable.]]>

<![CDATA[Job Description Currently, we are recruiting for a contract-to-hire Regulatory Specialist for our client. Our client is a leader in the packaging industry. In this role, you will work with Purchasing, Marketing, and Research & Development to insure that materials being used and purchased for manufacturing are in compliance with regulations surrounding use as a packaging material within the United States and abroad. Primarily packaging that is used in contact with foods, pharmaceuticals, and other regulated items. You will use your experience in interpreting regulations and your background in the sciences to advise internal and external clients on applications and labeling associated with packages and packaging materials. This opportunity is a first shift position and will eventually involve up to 25% travel to various manufacturing sites. Job Requirements Qualified candidates will possess a minimum of a Bachelor's Degree in Food Science, Chemistry, Material Science, or related field of study with two to five years of industry experience working in regulatory. Experience with regulations regarding pharmaceuticals, packaging materials, food ingredients, or related industries is preferred. Candidates must possess effective communication skills as well as excellent project management skills.]]>