Puerto Life Science Hiring For Quality Assurance Dept
We’re Hiring – Join Puerto Life Sciences Pvt. Ltd. (Sterile Industry Only)
Be part of a future-focused team committed to delivering world-class sterile products. We are inviting talented professionals for the following roles in Quality Assurance and Regulatory Affairs.
1. Sr. Executive – Quality Assurance
Experience: 5+ years
Key Responsibilities:
- Ensure GMP compliance in all QA activities
- Review BMR/BPR, handle IPQA, line clearance, deviation control
- Support internal/external audits and regulatory inspections
- Lead QMS operations including CAPA, Change Control, and compliance training
- Coordinate with validation, manufacturing, and QC teams
2. Officer – Quality Assurance
Experience: Up to 4 years
Key Responsibilities:
- Support documentation activities – BMR/BPR review, logbook maintenance
- Conduct IPQA and manage line clearance processes
- Assist in deviation investigation and document tracking
- Contribute to training, audits, and QMS documentation
3. Executive – Regulatory Affairs
Experience: 4+ years
Key Responsibilities:
- Prepare and review regulatory dossiers (CTD/eCTD) for global submissions
- Ensure timely coordination for product registration and renewals
- Handle regulatory queries and documentation for domestic & export markets
- Collaborate with QA, QC, and Production for dossier compilation and compliance
📨 To Apply Send your updated resume, current CTC, and notice period to: 📧 hr@puerto.in
🔖 Note: Candidates with experience in the sterile industry will be preferred.
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