- 7 PM
- 7 AM
- 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.
- Attain qualification for all assigned tasks and maintain individual training plan.
- Perform basic laboratory tasks, such as monitor pH, conductivity, test product samples, etc.
- Perform material movements, transfer raw materials, chemicals into, out of, across the production areas.
- Maintain facility and equipment through routine cleaning and sanitization, support 6S programs.
- Perform other duties as assigned.
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The Manufacturing Associate is responsible for the manufacturing of therapeutic proteins (API) under cGMP conditions.Associates are expected to execute process recipes, follow written procedures (SOPs), monitor equipment and processes, perform basic laboratory tasks, including pH ...
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The Manufacturing Associate is responsible for manufacturing therapeutic proteins (API) under cGMP conditions. ...
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The Manufacturing Associate is responsible for the manufacturing of therapeutic proteins under cGMP conditions.Associates are expected to execute process recipes, follow written procedures (SOPs), monitor equipment and processes, perform basic laboratory tasks, including pH, cond ...
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+The Biotechnologist Associate / Manufacturing Associate is responsible for the manufacturing of therapeutic proteins (API) under cGMP conditions. · + · , · , · ...
Portsmouth, NH1 month ago
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+ +The Manufacturing Associate is responsible for the manufacture of therapeutic proteins under cGMP conditions. · + +Execute process recipes and follow written procedures (SOPs) · Monitor equipment and processes · Perform basic laboratory tasks such as pH monitoring, conductivit ...
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TekWissen is a global workforce management provider headquartered in Ann Arbor, Michigan that offers strategic talent solutions to our clients world-wide. · ...
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The Manufacturing Associate is responsible for the manufacture of therapeutic proteins (API) under cGMP conditions. · Set up, operate equipment, and monitor production processes, · Maintain facility and equipment through routine cleaning and sanitization, · Perform basic laborato ...
Portsmouth1 month ago
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The Manufacturing Associate is responsible for the manufacturing of therapeutic proteins under cGMP conditions.Associates are expected to execute process recipes, follow written procedures (SOPs), monitor equipment and processes, perform basic laboratory tasks, including pH, cond ...
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The Manufacturing Associate is responsible for the manufacture of therapeutic proteins (API) under cGMP conditions. Level III associates are expected to be fully proficient in executing process recipes, following written procedures (SOPs), monitoring equipment and processes. · ...
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The Biotechnologist Associate / Manufacturing Associate is responsible for the manufacturing of therapeutic proteins under cGMP conditions. · Associates are expected to execute process recipes, follow written procedures (SOPs), monitor equipment and processes. · They are expected ...
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We are hiring Manufacturing Associate for one of our clients. · Set up, operate equipment, and monitor production processes. · Attain qualification for all assigned tasks. · Perform basic laboratory tasks. · ...
Portsmouth1 month ago
Manufacturing Associate - Portsmouth - LanceSoft Inc
Description
Title:
Biotechnologist Associate Location:
Portsmouth, NH – 03801 Duration: 12 Months Nights
Submit your CV and any additional required information after you have read this description by clicking on the application button.
- every other weekend.
Description:
The Manufacturing Associate is responsible for the manufacturing of therapeutic proteins (API) under cGMP conditions.
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.
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.
Administrative tasks – attending shift exchange, meetings, sending/receiving emails, participating in projects. xhuatnn
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Manufacturing Associate
BioTalent- Portsmouth
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Manufacturing Associate
Only for registered members Portsmouth, NH
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Manufacturing Associate
Only for registered members Portsmouth, NH
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Manufacturing Associate
Only for registered members Portsmouth, NH
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Manufacturing Associate
Only for registered members Portsmouth
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Manufacturing Associate
Only for registered members Portsmouth
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Manufacturing Associate
Full time Only for registered members Portsmouth
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Manufacturing Associate
Only for registered members Portsmouth
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Manufacturing Associate
Only for registered members Portsmouth
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Manufacturing Associate
Only for registered members Portsmouth
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Manufacturing Associate
Only for registered members Portsmouth
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Manufacturing Associate
Only for registered members Portsmouth
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Manufacturing Associate
Only for registered members Portsmouth, NH
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Manufacturing Associate
Only for registered members Portsmouth
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Manufacturing Associate
Only for registered members Portsmouth
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Manufacturing Associate
Only for registered members Portsmouth
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Manufacturing Associate
Only for registered members Portsmouth
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Manufacturing Associate
Only for registered members Portsmouth
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Manufacturing Associate
Only for registered members Portsmouth
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Manufacturing Associate
Only for registered members Portsmouth