MPharm Job at Micro Crispr Pvt. Ltd | Apply Now for the Manufacturing Associate Role
Micro Crispr Pvt. Ltd. is hiring an Executive or Sr. Executive – Downstream Process (Biologics) to join its advanced manufacturing division. This MPharm Job is designed for professionals with 1–5 years of experience in purification techniques like chromatography and TFF. Candidates with a degree in Biotechnology, Microbiology, or M.Pharm will lead downstream activities under strict GMP conditions, ensuring the purity and consistency of life-changing viral vectors and biologics.
- Job Role: Manufacturing Associate – Downstream
- Location: Vapi, Gujarat, India
About The Company
Micro Crispr Pvt. Ltd. is an innovative biotechnology firm dedicated to shaping the future of advanced therapeutics. The company specializes in the development and manufacturing of viral vectors, vaccines, and monoclonal antibodies, bridging the gap between complex process science and scalable manufacturing reality. Operating with a “patient-first” mindset, Micro Crispr maintains a rigorous GMP-regulated environment and utilizes state-of-the-art single-use technologies. The organization fosters a collaborative culture where Manufacturing, Quality, and Validation teams work together to deliver high-purity, life-changing treatments to patients globally.
About the Role
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.
Education
- M.Pharm (Biotech).
Requirements
- 1–5 years of experience in downstream processing within biologics, vaccines, biosimilars, monoclonal antibodies, or viral vectors.
- 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 close attention to detail.
- Comfortable working in cleanroom environments.
