What are the responsibilities and job description for the Manufacturing Associate – Viral Vector / Gene Therapy position at Pharmaceutical Company?
We are seeking a Manufacturing Associate with hands-on experience in cGMP biopharma manufacturing to support viral vector production. This role involves both upstream and downstream processes, ensuring high-quality production of clinical and commercial products in a regulated environment.
Key Responsibilities
- Perform upstream virus production (cell culture, bioreactors) and downstream purification (chromatography, filtration)
- Prepare media, buffers, and manufacturing support materials
- Set up and maintain manufacturing equipment, including chromatography columns
- Execute manufacturing activities in compliance with cGMP and SOPs
- Support process deviations and investigations (data collection, trending, reporting)
- Review and maintain batch records, SOPs, and documentation
- Perform routine calculations and ensure accurate record-keeping
- Maintain equipment, safety procedures, and compliance standards
- Support tech transfer activities from R&D to manufacturing
Requirements
- Bachelor’s degree in Biology, Biotechnology, or related field
- 2–5 years of experience in biopharma / biotech manufacturing
- Hands-on experience with viral vectors (AAV, Lentivirus, etc.) preferred
- Strong knowledge of cGMP, SOPs, and batch documentation
- Experience in upstream/downstream processing
Salary : $30 - $33