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The Expression group is responsible for non-GMP protein drug lead generation, supporting the various Pfizer research units and their pre-clinical therapeutic in-vitro and in-vivo needs. The Expression group is responsible for non-GMP protein drug lead generation, supporting the various Pfizer research units and their pre-clinical therapeutic in-vitro and in-vivo needs.
ExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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Experience as owner’s rep for pharmaceutical, biotech R&D lab design & operations, clinical/GMP facilities, and lab/office space optimization preferred. At Novo Nordisk we recognize that it is no longer good enough to aspire to be the best company in the world.
Full-timeExpandApply NowActive JobUpdated 14 days ago - UpvoteDownvoteShare Job
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Ultragenyx has multiple Gene Therapy programs in development, a robust pipeline, and we are building a state of the art GMP manufacturing facility in Bedford, MA. Join our team! The Ultragenyx Gene Therapy team is headquartered in Cambridge and this position will be located within our state of the art GMP Manufacturing facility in Bedford, MA. We are looking for exceptional individuals who share our passion for developing novel therapies to treat rare diseases and advancing the field of gene therapy.
Full-timeExpandApply NowActive JobUpdated 10 days ago - UpvoteDownvoteShare Job
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5-10 years' experience in maintenance planning, scheduling and/or MRO inventory management in a GmP environment. Ensures GMP and non-GMP maintenance work is completed and documented in the most efficient and compliant manner in alignment with Lantheus Quality Management Systems.
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GMP - Aseptic and non-Aseptic Areas and Non GMP Area - Offices spaces. Test continuity of circuit to insure electrical compatibility and safety of components, using testing instruments, such as ohmmeter, battery and buzzer, and oscilloscope.
Full-timeExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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Reporting to the Director, Quality Assurance, GMP, the Product Complaint Specialist/Senior Specialist will support the management of product complaints to ensure compliance with global regulations associated with marketed and investigational products.
Full-timeExpandApply NowActive JobUpdated 11 days ago - UpvoteDownvoteShare Job
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3+ Year working directly with a life science software product in a compliant environment (CLIA, GMP, IVD etc.) 3+ years of direct product management, product marketing, technical marketing, applications or pre-sales scientific support experience in life sciences or medical device industry with domain expertise in protein biomarker applications.
ExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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It operates across Good Clinical Practice (GCP), Good Pharmacovigilance Practice (GVP), Good Manufacturing Practice (GMP), Good Laboratory Practice (GLP) and Computer Systems Compliance (CSC) (together, GxP.
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1 - 2 years previous experience in a GMP laboratory desired; internship experience considered. The QC Microbiologist I, Environmental Monitoring will learn, understand, and perform routine entry level sampling of cleanrooms and utilities according to written procedures under cGMP conditions; as well as tasks involved with clerical and logistical laboratory tasks.
ExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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Ensure systems compliance with applicable GLP/GMP/BSL# (PM, PV, OQ etc., where applicable) Managing the removal of wastes, the monthly radiation dose check for all x-ray instrumentation, the maintenance of the deionized water, fume hoods and bottled gases, etc.
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Ability to document experimental results to GLP/GMP standards. Ability to work in a Biosafety Level 2 lab. Ability to document experimental results to GLP/GMP standards. Must be able to wear personal protective equipment (gloves, face shields/safety glasses, latex, or nitrile gloves, etc.
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Early-stage analytical testing (cGMP and non-GMP) Knowledge of relevant GMP and quality guidelines. Degree in analytical chemistry, chemistry, biochemistry, pharmaceutical sciences, or related field required.
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The Telecom Technician will participate in the installation or maintenance and inspection of telecommunication systems and associated processes. Oversees or participates in data cable installations, open wiring, with conduit and on cable trays.
ExpandApply NowActive JobUpdated 11 days ago - UpvoteDownvoteShare Job
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Follow all GMP and Safety Policies filling out appropriate paperwork. Filling out appropriate paperwork, forms as required for GMP. Maintain a clean and safe work environment by adhering to all GMP and Safety policies.
ExpandApply NowActive JobUpdated 4 days ago - UpvoteDownvoteShare Job
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Ensure projects are carried out in compliance with regulatory requirements (GMP, ISO, MDD/MDR) & LeMaitre policy & procedure requirements. Ensure projects are carried out in compliance with regulatory requirements (GMP, ISO, MDD/MDR) & LeMaitre policy & procedure requirements.
ExpandApply NowActive JobUpdated 7 days ago
gmp job Company: Genoskin in Wilmington, MA
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