Job Title Options (Choose One)
Executive / Sr. Executive – Downstream Process ( Biologics)
(Avoid Production Executive. Too small for the gravity of this work.)
About the Role
Join a team shaping the future of advanced therapeutics, where every purification step brings life-changing treatments closer to patients.
As part of the Manufacturing team, you will support downstream processing of viral vectors and biologics — ensuring purity, consistency, and compliance within a GMP-regulated environment.
This role is ideal for professionals who enjoy translating process science into scalable manufacturing reality.
Key Responsibilities
- Execute downstream manufacturing activities including filtration, chromatography, and bulk formulation under GMP conditions.
- Prepare buffers, solutions, and process materials as per approved batch records.
- Operate and maintain downstream equipment such as TFF systems, AKTA chromatography skids, depth filters, and associated single-use technologies.
- Monitor critical process parameters and document activities in real time following GDP practices.
- Support technology transfer and process scale-up activities.
- Troubleshoot process deviations and assist in investigations.
- Work closely with Upstream, QA, QC, and Validation teams to ensure smooth batch execution.
- Maintain strict adherence to aseptic practices, safety guidelines, and contamination control strategies.
Ideal Candidate Profile
- 1–5 years of experience in downstream processing within biologics, vaccines, biosimilars, monoclonal antibodies or viral vector.
- Hands-on exposure to purification techniques such as:
Chromatography
Tangential Flow Filtration (TFF)
Ultrafiltration/Diafiltration
Depth filtration
- Familiarity with GMP documentation and manufacturing workflows.
- Strong problem-solving mindset with high attention to detail.
- Comfortable working in cleanroom environments.
Education
- M.Sc / B.Sc in Biotechnology, Microbiology, Biochemistry
- B.Tech / M.Tech in Biotechnology or Bioprocess
- M.Pharm (Biotech)
