Milan Laboratories India Private Limited is hiring an IPQA Officer for its pharmaceutical manufacturing operations in Panvel, Maharashtra. Candidates with a B.Pharm or M.Pharm qualification and 1–3 years of experience in In-Process Quality Assurance (IPQA) can apply.
The selected candidate will be responsible for monitoring in-process manufacturing and packing activities, ensuring GMP compliance, conducting line clearance, and supporting quality documentation and CAPA activities.
Job Details
| Particulars | Details |
|---|---|
| Company | Milan Laboratories India Private Limited |
| Job Title | IPQA Officer |
| Job Location | Panvel, Maharashtra – 410209 |
| Qualification | B.Pharm / M.Pharm |
| Experience | 1–3 Years |
| Department | In-Process Quality Assurance (IPQA) |
| Industry | Pharmaceutical Manufacturing |
| Gender Preference | Male candidates preferred due to rotational shifts |
| Application Email | talentpool@milanlabs.com |
Position: IPQA Officer
Milan Laboratories is looking for an IPQA Officer to ensure in-process quality compliance during pharmaceutical manufacturing operations in accordance with Good Manufacturing Practices (GMP).
Key Responsibilities
- Monitor in-process activities during manufacturing and packing operations.
- Ensure compliance with GMP, SOPs, and regulatory requirements.
- Perform line clearance and in-process quality checks.
- Review manufacturing and quality documentation.
- Handle deviations and non-conformances.
- Provide support for Corrective and Preventive Actions (CAPA).
- Coordinate with Production and QA teams to maintain quality compliance.
Eligibility Criteria and Qualifications
Candidates applying for the IPQA Officer position should meet the following requirements:
- B.Pharm or M.Pharm qualification.
- 1–3 years of experience in IPQA within pharmaceutical manufacturing.
- Experience in a pharmaceutical manufacturing unit is preferred.
- Knowledge of GMP, SOPs, and regulatory standards.
Required Skills
- Knowledge of Good Manufacturing Practices (GMP).
- Understanding of Standard Operating Procedures (SOPs).
- In-process quality monitoring.
- Line clearance and in-process checks.
- Documentation review.
- Deviation and non-conformance handling.
- CAPA support.
- Coordination with Production and Quality Assurance teams.
- Strong attention to detail.
Application Details – How to Apply
Interested and eligible candidates can share their updated resumes through email.
Email: talentpool@milanlabs.com