Walk-In Interview 10th & 11th Oct- Upstream Specialist - Biosimilars

Relocation Note: This position is based in Ahmedabad. Candidates must be willing to relocate to Ahmedabad, Gujarat.

Walk-in Details:

• Interview Location: Pune
• Venue: Hotel Sayaji , 135/136, Mumbai-Banglore Bypass Highway, Shankar Kalat Nagar, Wakad, Pune, Pimpri-Chinchwad, Maharashtra 411057
• Date & Time: 10th & 11 October 2026 at 9:00 AM
• Education: Life science Graduate / Postgraduate (M.Sc./B.E./B.Tech/M.Tech (Biotechnology/Microbiology)
• Total Years of Experience: 4 to 10 Years
• Job Location: Ahmedabad

We are looking for an experienced Upstream Manufacturing Professional for our state-of-the-art Biosimilars Manufacturing site based in Ahmedabad. In this role, you will manage upstream processes for mammalian cell culture, handle single-use bioreactors, and ensure strict compliance with cGMP and regulatory standards.

Key Responsibilities:

• Manage and execute Upstream Process operations focusing heavily on Mammalian Cell Culture and Monoclonal Antibodies (mAbs) production.
• Operate and handle various Cell Culture techniques and advanced Single-Use Bioreactors.
• Handle Perfusion Technology operations (mandatory requirement).
• Participate in equipment qualification, validation, and QMS activities during initial stages, followed by routine batch manufacturing.
• Ensure adherence to Good Manufacturing Practices (GMP) and Good Documentation Practices (GDP).
• Face and support regulatory audits with complete transparency and compliance.

Desired Candidate Profile:

• Education: Life Science Graduation or Post-Graduation (B.Tech/B.E./M.Tech/M.Sc in Biotechnology, Biochemistry, Bio-Technology, Chemical Engineering, B.Pharma, or related life science disciplines).
• Industry Experience: 4+ years of relevant experience specifically from the Pharmaceutical industry with exposure to Drug Substance (Biosimilars) manufacturing.
• Proven hands-on background in mammalian cell culture, single-use bioreactors, and perfusion technology.
• Good working knowledge of regulatory audits (USFDA, EMA, etc.), cGMP, and GDP standards.
• Strong communication, interpersonal, and problem-solving skills.

Interested candidates Please Walk-in for an interview along-with their updated CVs, as per the schedule. Since it is a Walk-in Interview , please share the details within your groups and connection and bring along your references having similar experience as mentioned above.