Position: Biotechnologist Associate
Location: Portsmouth, NH (Onsite)
Duration: 12 months contract with possible extension or full time conversion
Pay Rate Day Shift: $23/hr. on W2 (OT every 2nd Week 20 hr. OT with hourly rate of $34/hr.)
During one week you would be only working two 12-hour shifts per week. (5 days off that week)
The following week, while you are working 60 hours (five 12-hours shifts), you are getting paid x1.5 (20 hours of overtime every two weeks)
Days shift 7AM-7PM 12 hour shift
This role is for fresh grads who have a bachelor's degree in life sciences.
Job Description :
The Manufacturing Associate is responsible for the manufacture of therapeutic proteins (API) under cGMP conditions. Level I 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.
Daily Task :
The Biotechnologist Associate is responsible for the manufacturing of therapeutic proteins (API) under cGMP conditions.
This role is for fresh grads who have a bachelor's degree in biotechnology.
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.
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 plans.
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. Must be willing to grow and work in a "clean room" environment.
Administrative tasks – attending shift exchange, meetings, sending/receiving emails, participating in projects.
Perform other duties as assigned.
Qualifications:
bachelor's degree in life sciences.
some prior experience in a manufacturing setting preferred
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