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The candidate will work closely within the team and across functional groups to ensure smooth transition of new cell therapy products and processes from process development into GMP manufacturing, and execution of technical training of MFG personnel.
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Astellas is announcing a QC Analyst I Microbiology opportunity at their Astellas Institute for Regenerative Medicine (AIRM) site in Westborough, MA. Purpose:AIRM is seeking a highly motivated individual to join us as a QC Microbiology Associate I. This position provides Quality Control Microbiology support to all aspects of a GMP environmental monitoring program and product testing.
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Pharmaceutical facilities including GMP Aseptic and non-Aseptic Areas and Non GMP Areas. Assemble pipe sections, tubing or fittings using couplings, clamps, screws, bolts, cement, plastic solvent, caulking, soldering or brazing equipment.
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Works with materials that include carbon steel, stainless steel, plastics, fiberglass, copper, (brazed, soft soldered and pro-press); The Pipefitter will participate in the installation or maintenance and inspection of HVAC, Utility and Process piping systems.
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You must adhere to all safety, SQF, GMP, and housekeeping rules and regulations. It is importa Forklift Operator, Lift Operator, 3rd Shift, Forklift, Operator, Staffing, Manufacturing. As a sit-down forklift operator, your primary responsibilities will be to retrieve and stage raw materials for kitchen processing in a constructive manner.
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Comply to all safety, SQF, and GMP practices. Ken’s Foods, manufacturer of Ken’s Salad Dressing and Sweet Baby Rays, is a dynamic company, family-owned and -operated since 1958. Follow the “pig program” following procedure to retrieve/recover pigs and place them on appropriate storage boards.
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Working knowledge of Validation Lifecycle Approach (DQ, IQ, OQ, PQ, PV, and RQ) Knowledge of applicable US and worldwide regulatory requirements ( GMP, GDP, ICH) Ability to develop and/or review protocols using design documents and user requirements.
ExpandApply NowActive JobUpdated 14 days ago - UpvoteDownvoteShare Job
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Knowledge of QA systems and GMP compliance requirements including regulations and standards affecting device, biologics, and pharmaceutical products. Manage and oversee the interrelated function activities including design control with R&D, Manufacturing Science and Technology (MS&T), Supply Chain, Program Management, Commercial, Medical, Pharmacovigilance, and Regulatory Affairs.
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The QC Microbiology inspector reviews laboratory tests within a fast-paced GMP environment in support of one or more of the following areas: raw materials, in-process, final bulk product, and/or validation.
ExpandApply NowActive JobUpdated 27 days ago - UpvoteDownvoteShare Job
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Must follow Good Manufacturing Practices (GMPs) and to ensure GMP compliance of fellow associates. Overview: Polar Beverages is looking to add a Bilingual Human Resources Generalist (English/Spanish) to their HR team.
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Operates all manual and automated material handling equipment including Powered Industrial Trucks (PIT) to transport controlled and indirect materials within a GMP warehouse environment. Materials Operations is also responsible for supply chain security compliance, hazardous materials, import/export, inventory management & control, warehouse operations and other value-added logistics.
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BS Degree preferred but not required (Biology) Facilitating the training for staff and management team in Food Safety, GMP, and HACCP, Sanitation, Allergens policies, and procedures. BS Degree preferred but not required (Biology) Facilitating the training for staff and management team in Food Safety, GMP, and HACCP, Sanitation, Allergens policies, and procedures.
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In this role, you will play a crucial part in ensuring the GMP method performance of analytical chemistry and molecular-based assays. Experience in Quality Control roles supporting GMP testing/manufacturing.
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Cell culture, gmp, purification. You'll have the opportunity to leverage state-of-the-art programs such as LIMS SAP automated control systems DCS PLC PI and more. Skillfully preparing equipment for operation including cleaning and sterilization processes CIP/SIP.
$30 - $32 an hourExpandApply NowActive JobUpdated 28 days ago - UpvoteDownvoteShare Job
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Understanding of GMP product manufacturing from initiation through release capabilities preferredEOE/F/M/D/V. Experience in a regulated biotechnology or pharmaceutical field or CDMO strongly preferred.
$66.14 an hour depends on experienceExpandUpdated 26 days ago
gmp job in Westborough, MA
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