Mepro Hiring QC, RA, PPIC
- Company Overview
- Job Role & Responsibilities
- Eligibility / Qualifications
- Location & Salary
- Application Process
- Why Join Mepro Pharmaceuticals?
- Frequently Asked Questions (FAQs)
- Summary Table
Meta Title: Mepro Pharma Senior QC & RA Roles | B.Pharm/M.Pharm Vadodara
Meta Description: Multiple vacancies at Mepro Pharmaceuticals, Vadodara for QC, RA, PPIC roles. Open for B.Sc/M.Sc/B.Pharm/M.Pharm with 2–12 years experience.
Join Mepro Pharmaceuticals Pvt. Ltd. (Unit-III) in Vadodara — a purpose-driven manufacturer committed to high-quality pharmaceutical products and patient safety. Mepro is hiring experienced professionals across Quality Control (QC), Regulatory Affairs (RA), Quality Management System (QMS) review, AMV validation leadership, and PPIC (Production Planning & Inventory Control). If you are motivated by regulatory excellence, scientific rigor, and cross-functional ownership, these roles offer meaningful impact and career growth.
Company Overview
Mepro Pharmaceuticals Pvt. Ltd. is a trusted manufacturer in the pharmaceutical domain with a clear focus on compliance, product quality and lifecycle management. The company operates cGMP-compliant facilities and emphasizes systematic quality processes, regulatory preparedness and continuous improvement. Working at Mepro positions you to contribute directly to healthcare outcomes by ensuring that safe, effective medicines reach patients reliably.
Job Role & Responsibilities
Below are the open roles at Mepro Pharmaceuticals (Unit-III), Vadodara. Each role includes the core responsibilities and the technical/leadership expectations.
Quality Control — Sr. Executive (QMS Section Reviewer)
Qualification: B.Sc / M.Sc
Experience: 8–10 years
Key Responsibilities:
- Review and approve QMS documentation ensuring alignment with GDP/GLP and regulatory requirements.
- Maintain document control, ensure SOPs are current and audit-ready.
- Coordinate with QA and QC teams during internal and external audits.
- Drive data integrity and compliance initiatives across the laboratory.
Quality Control — Asst. Manager (AMV Lead)
Qualification: B.Sc / M.Sc
Experience: 10–12 years
Key Responsibilities:
- Lead AMV (Analytical Method Validation) activities across HPLC, GC, UV and allied platforms.
- Review validation protocols, reports, and SOPs; supervise AMV team and method transfers.
- Troubleshoot analytical issues, mentor junior scientists and coordinate with QA for compliance.
- Support audits, instrument qualification, and continual improvement of lab practices.
Regulatory Affairs — Senior Position (Team Lead)
Qualification: B.Pharm / M.Pharm (or B.Sc/M.Sc with regulatory experience)
Experience: 8–12 years for B.Pharm/M.Pharm; 2–6 years for B.Sc/M.Sc regulatory profiles
Key Responsibilities:
- Prepare, review and submit regulatory dossiers (CTD, ACTD, country-specific formats).
- Track regulatory timelines, manage product lifecycle documentation and respond to regulatory queries.
- Assess CMC changes, identify regulatory risks and propose mitigation strategies.
- Coordinate cross-functionally with R&D, QC and Production for dossier support and post-approval commitments.
PPIC (Production Planning & Inventory Control) — Officer / Sr. Executive
Qualification: Any Graduate (pharma-experienced preferred)
Experience: 6–10 years
Key Responsibilities:
- Forecast inventory and schedule production to meet demand while minimizing stockouts/overstock.
- Raise material orders, coordinate deliveries and manage vendor qualification inputs with QA/RA.
- Prepare cost sheets, maintain stock statements and support artwork/vendor qualification workflows.
- Liaise with cross-functional teams and assist VP Operations on special projects.
Eligibility / Qualifications
Relevant courses (comma-separated): B.Pharm, M.Pharm, B.Sc (Chemistry, Microbiology, Life Sciences), M.Sc (Analytical Chemistry, Pharmaceutical Chemistry, Biotechnology), B.E/B.Tech (where applicable), Diploma in Pharmacy, MBA (Operations/Production) — list not exhaustive.
Experience Range: 2 to 12 years depending on the role. Specific experience requirements are listed per role above.
Core Skills Across Roles:
- Strong understanding of GMP, GLP, GDP and regulatory expectations.
- Proven experience with analytical instruments (HPLC, GC, UV) for QC and AMV roles.
- Excellent documentation, drafting and communication skills (especially for QMS and RA roles).
- Cross-functional collaboration, process-orientation and problem-solving mindset.
Location & Salary
Location: Mepro Pharmaceuticals Pvt. Ltd. (Unit-III), Vadodara, Gujarat
Compensation: Competitive and aligned with experience, seniority and industry benchmarks. Specific offers will be based on skills, current CTC and role-fit.
Application Process
Interested candidates should email an updated CV with a clear subject line mentioning the department (e.g., “Application – Asst Manager AMV, Mepro Unit-III”) to the careers mailbox below. Please include current CTC, expected salary and notice period.
📧 Email: careers@mepro.in
⚠️ Apply before November 30, 2025 to ensure timely consideration — early applicants will be prioritized.
Why Join Mepro Pharmaceuticals?
- Be part of a compliance-first organization with strong focus on product quality and regulatory success.
- Work in a collaborative environment that emphasizes technical excellence and employee development.
- Opportunity to lead and influence critical quality and regulatory functions that impact patient safety.
- Competitive pay, learning pathways and exposure to multi-functional projects across QC, RA and supply chain.
Frequently Asked Questions (FAQs)
1. What roles are open at Mepro Pharmaceuticals (Unit-III)?
Openings include QC Sr. Executive (QMS reviewer), Asst. Manager AMV, Senior Regulatory Affairs (Team Lead), Regulatory positions (2–6 years profile), and PPIC Officer/Sr. Executive.
2. What qualifications are required?
Qualifications vary by role: B.Sc/M.Sc/B.Pharm/M.Pharm and related degrees as listed. See the role-specific sections for exact requirements.
3. How do I apply?
Send your updated CV to careers@mepro.in with your current CTC, expected salary and notice period. Use the department name in the email subject.
4. Is there a deadline to apply?
Yes — apply before November 30, 2025 for priority review.
5. Will Mepro accept applications from candidates outside Vadodara?
Yes — candidates across India with suitable experience and willingness to relocate or commute are encouraged to apply.
Summary Table
| Category | Details |
|---|---|
| Company | Mepro Pharmaceuticals Pvt. Ltd. (Unit-III) |
| Vacancies | QC Sr. Executive (QMS), Asst. Manager AMV, Senior Regulatory Affairs (Team Lead), Regulatory Positions, PPIC Officer/Sr. Executive |
| Required Education | B.Sc, M.Sc, B.Pharm, M.Pharm, Diploma (Pharmacy), B.E/B.Tech, MBA (Operations) |
| Experience | 2 to 12 Years (role-dependent) |
| Location | Vadodara, Gujarat |
| careers@mepro.in | |
| Apply By | November 30, 2025 |
To apply for this job email your details to careers@mepro.in
