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The Manufacturing Associate I is responsible for the manufacture of therapeutic proteins (API) under current Good Manufacturing Practices (cGMP) conditions. They are expected to demonstrate a strong understanding of cGMP compliance while operating under supervision, and aseptic technique in handling of products and materials.
Full-timeExpandApply NowActive JobUpdated 3 months ago - UpvoteDownvoteShare Job
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A Calibration Technician must be able to safely complete monthly planned and demand maintenance tasks per assign cGMP procedures. Complete safety and cGMP training including classes, reads, and technical requirements as a trainee and a trainer.
Full-timeExpandApply NowActive JobUpdated 2 months ago - UpvoteDownvoteShare Job
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The Manufacturing Associate is responsible for the manufacturing of therapeutic proteins (API) under cGMP conditions. They are expected to attain a basic understanding of cGMP compliance while training under close supervision, demonstrating aseptic technique in handling of products and materials.
Full-timeExpandApply NowActive JobUpdated 27 days ago - UpvoteDownvoteShare Job
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Set up, operate equipment, and monitor production processes, including clean-in-place (CIP) and steam-in-place (SIP) operations and report production in written and electronic documents in accordance with good manufacturing practice (GMPs) and good documentation procedures (GDPs), review documentation as appropriate.
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Title: Manufacturing Associate I Location: Portsmouth, NH Industry: Pharmaceutical Hours: Days: 7 AM - 7 PM: 12hr days Every other weekend (rotating schedule including weekends) Salary: Days: $23.25 hourly paid weekly (Benefits Available) Employment Type: 1 year contract Summary: The Manufacturing Associate is responsible for the manufacturing of therapeutic proteins (API) under cGMP conditions.
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Possesses thorough knowledge of current domestic and international standards and regulations related to pharmaceutical dosage forms/devices, (e.g., cGMP, GLP, ICH guidelines and guidance documents) and how to apply them to products pending release, and marketed products.
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The Manufacturing Associate is responsible for the manufacture of therapeutic proteins (API) under cGMP conditions. The Manufacturing Associate is responsible for the manufacture of therapeutic proteins (API) under cGMP conditions.
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The Biotechnologist/Manufacturing Associate I is responsible for the manufacture of therapeutic proteins (API) under current Good Manufacturing Practices (cGMP) conditions. Working experience in manufacturing; cGMP setting preferred, and/or some experience as an Associate Level I in bio-pharma industry.
ExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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At least 15 years of experience with design, construction and qualification of large ($150M + ) cGMP biotechnology facilities, including at least one major Greenfield cGMP facility build completed.
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Must be willing to gown and work in a "clean room" environment. Perform material movements, transfer raw materials, chemicals into, out of, across the production areas. Associates are expected to execute process recipes, follow written procedures (SOPs), monitor equipment and processes, perform basic laboratory tasks, including pH, conductivity, sampling, and conduct routine sanitization tasks to maintain facility and equipment.
ExpandApply NowActive JobUpdated 4 days ago - UpvoteDownvoteShare Job
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Provides guidance and develops engineering design documents, technical evaluations, and test plans for cGMP process equipment. Preferably in automation manufacturing operations implementation, mechatronics design, system integration, and control systems development.
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Job Overview: The Manufacturing Associate plays a pivotal role in the production of therapeutic proteins (API) compliant with cGMP standards. Former Sig Sauer Employees. Job Overview: The Manufacturing Associate plays a pivotal role in the production of therapeutic proteins (API) compliant with cGMP standards.
Full-timeExpandApply NowActive JobUpdated 12 days ago - UpvoteDownvoteShare Job
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Independently understanding quality standards, cGMP s, and regulatory standards to support team in compliance of validation effort. Independently understanding quality standards, cGMP s, and regulatory standards to support team in compliance of validation effort.
Full-timeExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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The company s products and services include active pharmaceutical ingredients (API), stem cell therapies, drinking water sanitizers, vitamin B compounds, organic personal care ingredients, industrial preservatives and microbial control solution to combat viruses, bacteria and other dangerous pathogens.
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The Manufacturing Services Associate I is responsible for supporting all cGMP manufacturing production suites. They are expected to attain a basic understanding of cGMP compliance while training under close supervision, demonstrating aseptic technique and cross contamination awareness in handling of products and materials.
ExpandApply NowActive JobUpdated 3 days ago
cgmp job in Portsmouth, NH
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