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Home / Career Services / Opportunity Seekers / Job Postings / Life Science
Life ScienceAssay Development & Production Associate I or II - , Ann ArborDescription: Responsible for the development, testing, and manufacturing of immunoassay kits and reagents. Involved in all phases of kit product release, including choice of raw materials, selection of release criteria, validation, testing and optimizing of kit components. Requirements: Bachelor's or Master's Degree in a scientific field with 1-3 years of related experience, including immunoassay development and protein analytical techniques. Strong communication, documentation, and analytical skills. Flexible in responding to changing demands. Team player. E-mail resume to jobs@enzolifesciences.com Website: www.enzolifesciences.com (updated 9/2/2010)  Bioinformatics Analyst for Cancer Center - Center for Computational Medicine and Bioinformatics, University of Michigan, Ann Arbor Description: The Bioinformatics Analyst will determine best methods of bioinformatics and biostatistics for a variety of genomics, proteomics, and pathways analyses; focusing on next-generation sequencing and related assembly, alignment and annotation methods including developing workflows. This person will interact with the UM Sequencing core, and Cancer Center shared core facility personnel to smoothly transition data analysis and will be part of a core group of bioinformatics staff and research faculty. Requirements: A M.S. in Bioinformatics, Genetics, Biostatistics or related field is required. Candidates with Ph.D. are encouraged to apply. Laboratory experience is desired. Skill Set should include: Next-generation sequence assembly, alignment; proficiency with statistical packages (e.g. R) and micro-array analyses; programming skills in languages (e.g. PERL or Python), and SQL and relational databases. Experience with caBIG and grid computing is a plus. Excellent communication skills are required. E-mail resume to fmanion@umich.edu Website: http://umjobs.org/job_detail/51954/bioinformatics_analyst (updated 8/30/2010) Clinical Trial Manager - Esperion Therapeutics, Inc., Plymouth Description: Clinical Trial Manager will provide day-to-day operations management for clinical studies, including study start-up, conduct & close-out activities, which may be coordinated in conjunction with one or more CROs. Responsibilities include interactions with CROs, vendors, consultants & clinical sites; development of RFPs & scope of work documents, in collaboration with clinical team; & overseeing system for tracking & monitoring study progress to ensure adherence to timelines, SOPs and regulations. Requirements: Bachelor’s degree in a scientific or health related discipline & a minimum of 5 years of relevant experience at a CRO or pharmaceutical company. Therapeutics experience in cardiovascular and metabolic diseases is desirable. A working knowledge of GCP, ICH guidelines and FDA regulations. Ability to collaborate effectively with cross-functional team members and make necessary decisions. E-mail resume to ksmirnov@esperion.com Website: www.esperion.com (updated 8/30/2010) Microbiologist - Grand River APP, Grand Rapids Description: The microbiologist’s primary responsibility will be to support quality control and assurance by managing the environmental monitoring, water testing and client specific testing. These duties will include, but are not limited to: performing complex microbial analysis and assisting in method development and validation. Requirements: Microbiologist with a minimum of three to five years experience within a pharmaceutical, biopharmaceutical and/or biotechnology manufacturing environment (prefer aseptic filling environment experience). Must have strong interpersonal skills and be a team player. The person also must be able to communicate in a professional manner with clients and regulatory agencies. E-mail resume to asugden@grandriverapp.com Website: www.grandriverapp.com (updated 8/16/2010) Quality Assurance Associate/Specialist II - Grand River APP, Grand Rapids Description: The Quality Assurance Associate’s primary responsibility will be to support quality systems as they relate to the manufacturing and testing of cGMP drug products. These duties will include, but are not limited to: providing general support for environmental monitoring, raw material, stability and water testing programs, review of documentation and quality records, and supporting the Quality Management System. Requirements: QA/QC professional with a minimum of 5 to 10 years experience within a pharma, biopharma and/or biotech manufacturing environment (including aseptic filling environment). Must have strong interpersonal skills and be a team player. The person also must be able to communicate professionally with clients and regulatory agencies. E-mail resume to asugden@grandriverapp.com Website: www.grandriverapp.com (updated 8/16/2010) Lead Production Operator - Grand River APP, Grand Rapids Description: The lead production operator’s primary responsibility will be to perform various routine manufacturing tasks under the guidelines of established procedures and cGMP regulations under guidance of senior management and provide leadership through example to other employees. Requirements: High school diploma, bachelor’s degree in life sciences or equivalent training and/or experience is necessary. Two to five (2-5) years relevant experience in manufacturing or a laboratory environment is required. E-mail resume to asugden@grandriverapp.com Website: www.grandriverapp.com (updated 8/16/2010) Senior Biochemist - NanoVir, Kalamazoo Description: Position includes testing of novel antiviral drug candidates and in vitro proof on concept studies. Requirements: The ideal candidate will possess a broad skill set including expertise in cell and molecular biology and biochemistry. E-mail resume to Information@nanovirpharm.com Website: nanovirpharm.com (updated 7/20/2010) Senior Scientist - Compendia Bioscience, Ann Arbor Description: Join our growing team of scientists and engineers, with significant interactions with R&D, Scientific Content, and Operations. This role will have direct responsibility for developing new strategies to leverage cancer genomics data for target discovery, biomarker discovery and personalized medicine. Requirements: PhD required; research experience with cancer pathways, cancer drug development and / or cancer genomics a plus; a strong publication record is highly valued and pharma experience is valued.Able to review and synthesize scientific data. A strong understanding of basic biology, cancer biology and genomics.Have a clear record of scientific success in industry or academia. E-mail resume to careers2010@compendiabio.com (updated 7/14/2010) Bioinformatics Scientist - Compendia Bioscience, Ann Arbor Description: Join our growing team of scientists and engineers, with significant interactions with R&D, Product Management, Product Development, Scientific Content, and Operations. This role will have direct responsibility for developing strategies to process and manipulate novel types of high-throughput molecular profiling data. In addition, the role will support the organization in the implementation and operation of such strategies. Requirements: Bioinformatics, programming, and database experience are required; experience with Spotfire, Pipeline Pilot, R and SQL are a plus. Lead author publications and pharma experience are valued. A strong understanding of basic biology, genomics, microarrays, high-content data analysis and genome databases. Have strong computational skills; in particular, data parsing, data analysis and database implementation. Able to review and synthesize scientific data. E-mail resume to careers2010@compendiabio.com (updated 7/14/2010) Research Technician - Van Andel Institute, Grand Rapids Description: A full-time Research Technician position is available in the Vivarium. The primary responsibilities for this position will involve performing tasks related to the Germline Modification Program. Requirements: • Bachelor’s or Master’s degree in biological science • 3-5 years of post-graduate science related experience • Previous experience working with research animals is preferred • Good organizational and communication skills Qualified applicants should send a cover letter outlining research experience and interests, a curriculum vitae, and the names and address of three references to vari-employment@vai.org Subject Line: Req 1319 E-mail resume to vari-employment@vai.org Website: www.vai.org (updated 7/8/2010) Hybridoma Core Manager - Growing Michigan Biotech Company, S. Oakland County Description: Growing Michigan biotech company needs a Hybridoma core manager. Must have the ability to do production and characterization of monoclonal antibodies, including cell culture management. The ideal candidate resides in the greater Detroit Metro area and is seeking a challenging and rewarding career with an innovative and goal oriented company. Requirements: Training in cell culture maintenance or other hybridoma work. E-mail resume to ddday@mol-innov.com (updated 7/7/2010) Account Manager - Journal of Visualized Experiments, Ann Arbor Description: The Journal of Visualized Experiments, JoVE, is an independent publisher whose scientific video journals are indexed in PubMed. Since 2006 JoVE has produced & published over 600 video articles from leading labs and companies worldwide. JoVE recruits interesting research from academia & life science companies. Companies either sponsor video articles originating from academic labs or submit their own protocols for peer review demonstrating the value their product lines bring to a research lab. Requirements: Manage existing accounts; Develop new accounts; Preparing & presenting PowerPoint to companies; Organizing production timelines; Travel to conferences (~10%). Desired Skillsets; Direct technical sales experience; Scientific background (MSc or above preferred); Exceptional written & verbal communication skills; Organized; High computer proficiency which may include programming & developing Word or Excel Macros. E-mail resume to mark@jove.com Website: www.jove.com (updated 7/6/2010) Medical Technologist - Genetics Squared, Inc, Ann Arbor Description: Process tissue samples, perform various aspects of running and reporting results of assays, clean and maintain laboratory equipment, and assist with receipt and inspection of supplies in a CLIA-certified high-complexity laboratory. Ensure adherence to all quality and safety policies and procedures within a clinical laboratory. Actively participate in a team-oriented environment focused on customers and continuous improvement. Requirements: AS or BS in laboratory science or medical laboratory technology, or equivalent. Certification from a recognized professional association, such as American Medical Technologists, the Board of Registry of the American Association of Bioanalysts, or the Board of Registry for the American Society for Clinical Pathology. At least 2 years related job experience. Cytopathology experience highly desired. E-mail resume to jarthurs@genetics2.com Website: www.genetics2.com (updated 6/17/2010) Molecular Biologist or Biochemist - Swift Biosciences, Inc, Ann Arbor Description: Swift Biosciences, Inc is a rapidly growing Ann Arbor company that is developing novel research reagents and molecular diagnostic tools Requirements: Molecular biologist or biochemist, proficient in nucleic acid experimentation, and very experienced with quantitative and real-time PCR. Will consider either doctoral or postdoctoral scientists. E-mail resume to info@swiftbiosci.com (updated 6/14/2010) Associate Research Scientist, Bioanalytical - TSRL Inc, Ann Arbor Description: Responsibilities will include development of robust HPLC and LC-MS/MS methods for the analysis of drug candidates in biological matrices and analysis of study samples under both GLP and non-GLP conditions. Additional responsibilities include data analysis and reporting, contributions to research reports, as well as routine instrument maintenance. In this role, the candidate will support a team of scientists focused on discovery and development of pharmaceutical drug candidates. Requirements: BS in pharmaceutics, pharmacokinetics, pharmaceutical chemistry, medicinal chemistry, biochemistry, analytical chemistry, or a related science. Minimum 3 to 5 years of postgraduate experience Strong analytical skills 3-5 yr proficiency with HPLC and LCMSMS – ability to run routine samples, perform routine maintenance Proficiency with Microsoft suite – creation of reports & spreadsheets – Excel proficiency is a must Ability to follow SOPs and familiarity with GLP E-mail resume to jkowalski@tsrlinc.com Website: www.tsrlinc.com (updated 6/10/2010) |
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