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)