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Packaging, kitting, molecular biology, automation, perkin elmer, agilent, beckman coulter, biomek, centrifuge, pipettes, liquid handling, hamilton robotic system, Chemistry, Gmp, Biology, sap, reagent, reagent preparation, biotechnology, biochemistry.
Full-timeExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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2-3 years of experience working with analytical and biologic methodologies (chromatography, HPLC and ELISA in a regulated GMP/GLP Lab environment) HPLC, GC, KF, and UV/Vis. This position will also be working part of the time in the lab as the expert on HPLC and Empower in a GMP lab setting.
ExpandApply NowActive JobUpdated 8 days ago - UpvoteDownvoteShare Job
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5+ years of Quality Assurance experience in a QSR (GMP), disposable medical device environment. Multiple subassemblies for various OUs including SH, CRM, CRDN, PVH, PV, NM, etc. Assist with protocol and implement process validation procedures in accordance with QSR, FDA and international guidelines.
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Quality Assurance experience & knowledge of GMP required. Knowledge of Lean, Kaizen, and Continuous Improvement initiatives. Abiomed, part of Johnson & Johnson MedTech is recruiting for a Production Supervisor, 2 nd shift located in Danvers, MA.
Full-timeExpandApply NowActive JobUpdated 22 days ago - UpvoteDownvoteShare Job
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Strong experience with GMP, GLP, GxP, and other relevant regulatory standards. Expertise in cell therapy manufacturing, cloud-based data management systems, and medical device remediation. Proven ability to act as a mediator and communicator between technical teams and regulatory bodies.
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We own and operate a GMP biologics manufacturing drug substance. Possess prior work experience in a GMP, biotechnology and/or FDA regulated environment. Ensure the efficient maintenance and reliable operation of the process, HVAC and utility equipment needed to support a GMP manufacturing facility including supporting site laboratories.
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Project delivery types include design/build, negotiated GMP, Lump Sum Bidding, and CM at Risk contracts. We are a General Contractor/Construction Manager that is established pursuing a variety of commercial and light industrial projects throughout the nation.
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Knowledge of industry regulations and standards, such as FDA and GMP. Bachelor's degree in a related field, such as quality management, food science, or engineering. Minimum of [5] years of experience in quality management within the co-manufacturing or food manufacturing industry.
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Genoskin is a Franco-American biotech company with research facilities in Toulouse, France, and Salem, MA. The company creates, develops and specializes in first-in-human data generation for drug & vaccine developers as well as cosmetic companies and academic institutions.
$65,000 a yearFull-timeExpandApply NowActive JobUpdated 6+ months ago - UpvoteDownvoteShare Job
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ASQ Quality Engineer Certification (CQE)Six Sigma CertificationQuality by DesignApplied/industrial statistics experienceDetailed Knowledge of GMP, ISO and FDA design and development quality requirementsKnowledge of aseptic processing.
Full-timeExpandUpdated 13 days ago
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