SHANTHA BIOLOGICS – HIRING 2026
QA Validation | IPQA | IPQC | IPQM
Shantha Biologics, a leading organization in vaccine development and sterile injectable manufacturing, traces its origins to Shantha Biotechnics, one of India’s pioneering companies in recombinant human healthcare products.
Since 1993, the organization has been committed to developing and manufacturing affordable healthcare solutions, with a strong focus on vaccines and sterile injectable products. Its work is driven by innovation, quality, and equitable access to essential biologics.
📍 Location: Muppireddipally, Hyderabad, Telangana
1. Assistant Manager – QA Validation
Experience: 9–13 Years
Qualification:
- M.Pharm / M.Sc. in a relevant Life Sciences discipline.
- Hands-on experience in equipment, utility, CSV, filling line, and isolator qualification.
- Strong knowledge of cGMP, EU GMP Annex 1, and regulatory inspections, including USFDA/EMA requirements.
Key Responsibilities:
- Execute and review qualification and validation activities, including IQ/OQ/PQ, for equipment, utilities, filling lines, isolators, and AV systems.
- Manage the validation lifecycle, including risk assessments, deviations, CAPA, change controls, and validation documentation.
- Support process validation, cleaning validation, and computerized system validation activities.
- Act as a Validation SME during regulatory and customer audits.
2. Sr. Executive – IPQA / IPQC
Experience: 5–8 Years in IPQA/IPQC within biopharmaceutical manufacturing
Qualification:
- B.Pharm / M.Pharm / M.Sc. in a relevant discipline.
Key Responsibilities:
- Perform line clearance and in-process checks.
- Review BMRs, BPRs, and analytical testing records.
- Handle and support investigations related to deviations, OOS, OOT, change controls, and other quality events.
- Conduct shop-floor training and provide support during regulatory and customer audits.
3. Sr. Executive – IPQM
Experience: 5–8 Years in Biopharmaceutical Manufacturing
Qualification:
- B.Pharm / M.Pharm / M.Sc. in Microbiology, Biotechnology, Chemistry, or a related field.
Key Responsibilities:
- Review microbiology records and Bacterial Endotoxin Test (BET) results.
- Verify environmental and utility monitoring activities.
- Lead/support OOS, OOT, and contamination investigations, including CAPA implementation.
- Support sterility assurance and aseptic process monitoring activities.
📍 JOB LOCATION
Muppireddipally, Hyderabad, Telangana
📧 HOW TO APPLY
Interested and eligible candidates can share their updated CV at:
🔗 Apply Online
- Assistant Manager – QA Validation: Apply Online
- Sr. Executive – IPQA / IPQC: Apply Online
- Sr. Executive – IPQM: Apply Online
📢 If you are a qualified pharma/biopharma professional looking for an opportunity in QA, IPQA, IPQC, or IPQM, this could be a valuable career opportunity.
Please share this post with your professional network and eligible candidates.
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