Job Title: Manufacturing Biotechnologist 1
Job Duration: 12 months on W2
Job Location: Portsmouth, NH
Shift Timings: (Night Shift) Rotating night shift from 6:30 PM to 6:30 AM. One week consists of Monday, Tuesday, Friday, Saturday, and Sunday, followed by the next week consisting of Wednesday and Thursday. This follows a rotating 2-2-3 (Panama) schedule.
JOB DESCRIPTION:
This role will work on the floor primarily in the Buffer Prep area in Mid-Scale.
Workers will be working on Concentrates and with P11.
Please see attached description for additional details.
The Manufacturing Associate Level I 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.
Key Accountabilities:
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.
Administrative tasks attending shift exchange, meetings, sending/receiving
emails, participating in projects.
Perform other duties as assigned.