SHANTHA BIOLOGICS – HIRING 2026

SHANTHA BIOLOGICS – HIRING 2026

QA Validation | IPQA | IPQC | IPQM

SHANTHA BIOLOGICS – HIRING 2026

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:

hra@shanthabiologics.com

🔗 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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Job Category: Pharma
Job Type: Full Time
Job Location: Hyderabad

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