Puerto Life Sciences Pvt. Ltd., a leader in sterile pharmaceutical manufacturing, is hiring experienced professionals for Quality Assurance (QA) and Regulatory Affairs (RA) roles. The company seeks dedicated candidates to ensure compliance with Good Manufacturing Practices (GMP), regulatory submissions, and quality control in sterile products.
Open Positions:
- Senior Executive β Quality Assurance (5+ Years Exp)
- ReviewΒ BMR/BPR, conductΒ IPQA, handle deviations, and maintain document control.
- OverseeΒ line clearance,Β CAPA/change control, and support audits/training.
- QA Officer (Up to 4 Years Exp)
- EnsureΒ GMP compliance, assist in validation, and manageΒ QMS elements.
- Collaborate with cross-functional teams for regulatory adherence.
- Executive β Regulatory Affairs (4+ Years Exp)
- Prepare and submitΒ CTD/eCTD dossiersΒ for domestic & global markets.
- Coordinate with health authorities for approvals, renewals, and compliance.
About Puerto Life Sciences
“Life in Its Purest Form” β Puerto Life Sciences specializes in sterile pharmaceutical manufacturing, delivering high-quality injectables and healthcare products. The company is known for its GMP-compliant facilities, innovation-driven approach, and commitment to global regulatory standards.
Eligibility Criteria
- Education:Β B.Pharm/M.Pharm or related degree in Life Sciences.
- Experience:
- QA Roles:Β 4-5+ years inΒ sterile pharma (mandatory).
- RA Roles:Β 4+ years inΒ regulatory submissions (CTD/eCTD).
- Skills:Β Strong knowledge ofΒ GMP, QMS, IPQA, and regulatory guidelines (USFDA/EMA/WHO).
How to Apply
Interested candidates meeting the criteria should email the following to hr@puerto.in:
- UpdatedΒ Resume (PDF format)
- Current CTC & Expected Salary
- Notice Period
(Note: Only candidates with sterile industry experience will be considered.)
