What are the responsibilities and job description for the Biotechnologist Associate position at Katalyst CRO?
Company Description
Job 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 prod ucts and materials.
Roles & Responsibilities:
All your information will be kept confidential according to EEO guidelines.
- Katalyst Healthcares & Life Sciences is hiring entry level candidates for several positions for contract research in Clinical trials of drugs, biologics and medical devices.
- We have a few immediate job opportunities available in Drug Safety and Pharmacovigilance and Clinical Research field. We work with University hospitals, pharmaceutical companies and recruiting partners.
Job 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 prod ucts and materials.
Roles & 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 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 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 gown and work in a "clean room " environment.
- Administrative tasks – attending shift exchange, meetings, sending/receiving emails, participating in projects.
- Perform other duties as assigned.
- Food service.
- Cooks (can follow recipes).
- Pharmacy techs.
- Mechanical aptitude.
- Robotics.
- Computer skills (this is ever more important as our suites are more and more automated).
- EMTs.
- Tech Support.
- Anything in which they need to follow SOPs, Guidelines, industry regulations.
- Sig Sauer employees.
- Security guards.
- Nurses/nurses aids.
All your information will be kept confidential according to EEO guidelines.
