Intas Pharmaceuticals Ltd. is conducting a walk-in interview in Bengaluru for experienced professionals in Upstream, Downstream, Analytical Development, and QA.
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This is an excellent opportunity to work with one of India’s leading biopharma companies, known for advanced single-use bioreactor facilities, global regulatory exposure (US FDA, EMA), and cutting-edge data analytics tools like JMP and SIMCA.
📌 Key Hiring Details
- Company: Intas Pharmaceuticals Ltd.
- Departments: R&D (UPD, DSP, ADL), QA (Process QA)
- Experience: 3–10 Years (QA: 4–10 Years)
- Qualification: M.Sc / M.Tech / B.Pharm / M.Pharm (Biotech, Bioprocess, Biochemistry)
- Job Location: Ahmedabad (Biopharma Plant)
- Walk-In Location: Bengaluru
🗓 Walk-In Interview Details
- Date: 19 April 2026 (Sunday)
- Time: 09:30 AM – 05:00 PM
- Venue: Lemon Tree Hotel, Electronics City, Bengaluru
💼 Job Roles & Responsibilities
R&D – Upstream Process Development (UPD)
- Handle mammalian cell culture and bioreactors
- Perform process development, scale-up, and optimization
- Apply Design of Experiments (DoE) and data analytics
- Conduct process characterization for biosimilars
R&D – Downstream Process Development (DSP)
- Perform resin screening and purification optimization
- Execute viral validation and downstream processing
- Work on process scale-up and analytical interpretation
R&D – Analytical Development Lab (ADL)
- Conduct physicochemical characterization of recombinant proteins
- Operate instruments like HPLC, UPLC, CE
- Perform spectroscopy (CD, Fluorescence, DSC)
Quality Assurance – Process QA
- Review GMP documents, batch records, deviations
- Manage CAPA, change control, and audit observations
- Ensure batch release compliance and data integrity
- Support validation and regulatory audits
🎓 Qualifications & Skills Required
- M.Sc / M.Tech in Biotechnology, Bioprocess Engineering, Biochemistry
- B.Pharm / M.Pharm (for QA roles)
- Strong experience in biosimilars R&D or biotech industry
- Hands-on knowledge of bioreactors, analytical techniques, GMP compliance
- Understanding of global regulatory requirements (USFDA, EMA)
🌟 Why Join Intas Biopharma?
- Exposure to India’s largest single-use bioreactors
- Work in end-to-end USP & DSP facilities
- Experience global regulatory audits
- Use advanced tools like JMP & SIMCA
- Recognized as a Great Place to Work
- Strong growth in biopharmaceutical innovation
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