Planet Pharma
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Night Shift: 7PM - 7AM, rotating days, every other weekend
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.
Responsibilities
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 GMPs and GDPs.
Attain qualification for all assigned tasks and maintain individual training plan.
Perform basic laboratory tasks, such as monitoring pH, conductivity, testing product samples, etc.
Perform material movements, transfer raw materials, chemicals in and out of, and across the production areas.
Maintain facility and equipment through routine cleaning and sanitization, support 6S programs. Must be willing to gown and work in a "clean room" environment.
Employment Information
Seniority level: Not Applicable
Employment type: Full-time
Job function: Research, Manufacturing, and Science
Industries: Pharmaceutical Manufacturing, Biotechnology Research, and Medical Equipment Manufacturing
Benefits
Medical insurance
Vision insurance
401(k)
#J-18808-Ljbffr
Night Shift: 7PM - 7AM, rotating days, every other weekend
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.
Responsibilities
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 GMPs and GDPs.
Attain qualification for all assigned tasks and maintain individual training plan.
Perform basic laboratory tasks, such as monitoring pH, conductivity, testing product samples, etc.
Perform material movements, transfer raw materials, chemicals in and out of, and across the production areas.
Maintain facility and equipment through routine cleaning and sanitization, support 6S programs. Must be willing to gown and work in a "clean room" environment.
Employment Information
Seniority level: Not Applicable
Employment type: Full-time
Job function: Research, Manufacturing, and Science
Industries: Pharmaceutical Manufacturing, Biotechnology Research, and Medical Equipment Manufacturing
Benefits
Medical insurance
Vision insurance
401(k)
#J-18808-Ljbffr