Piramal Pharma Solutions is hiring an Executive – Quality Control to perform testing of raw materials, intermediates, and finished products while ensuring compliance with cGMP, regulatory, and company standards.
Roles & Responsibilities
- Conduct chemical and instrumental analysis (HPLC, GC, UV-Vis, IR, Karl Fischer, TOC) of raw materials, intermediates, and peptide APIs.
- Perform peptide-specific analytical techniques (reverse-phase HPLC, ion-exchange HPLC, amino acid analysis, peptide mapping).
- Execute method validation, verification, and transfer as per ICH guidelines.
- Maintain and review analytical documentation (SOPs, STPs, specifications, validation protocols).
- Ensure compliance with cGMP, GLP, and data integrity practices.
- Support OOS/OOT investigations, root cause analysis, and CAPA implementation.
- Monitor calibration and maintenance of analytical instruments.
- Prepare samples and documents for regulatory submissions (DMF, ANDA filings).
- Coordinate with QA, RA, Production, and R&D for batch release.
- Participate in regulatory audits (USFDA, EUGMP, WHO).
Experience & Qualifications
- 1–4 years of QC experience in pharmaceutical/chemical/API manufacturing.
- Hands-on experience with HPLC, GC, UV-Vis, Karl Fischer, TOC.
- Strong knowledge of cGMP, GLP, and regulatory guidelines.
- Master’s degree in a relevant field.
- Preferred: Experience in a USFDA/EUGMP-approved peptide/API company.
About Piramal Pharma Solutions
Piramal Pharma Solutions (PPS) is a leading Contract Development and Manufacturing Organization (CDMO) offering end-to-end drug development and manufacturing services. With facilities in North America, Europe, and Asia, PPS provides:
- Drug discovery & development
- Clinical trial supplies
- Commercial API & finished dosage manufacturing
- Specialized services (HPAPI, antibody-drug conjugates, sterile fill/finish, peptides, biologics, vaccines, gene therapies)
Piramal Group, with over 30 years of expertise, follows ethical, inclusive, and sustainable growth practices.
Why Join Piramal?
✅ Global exposure in pharmaceutical manufacturing
✅ Regulatory-compliant work environment (USFDA, EUGMP, WHO)
✅ Career growth in a leading CDMO
✅ Equal opportunity employer (diversity & inclusion-focused)
How to Apply
Job ID: 8654
Location: Navi Mumbai, Maharashtra, India
Experience: 1–4 years
Job Category: Quality Control