Multiple openings at Mepro Pharmaceuticals Unit-III, Vadodara! Urgent requirement in Quality Control, Quality Assurance & Regulatory Affairs. Excellent opportunities for experienced professionals in pharma jobs Gujarat and pharmaceutical careers in India.
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About the Company
Mepro Pharmaceuticals Pvt. Ltd., committed to humanity, is a leading WHO-GMP certified pharmaceutical company based in Vadodara, Gujarat. With state-of-the-art manufacturing facilities (including Unit-III), Mepro specializes in high-quality formulations across multiple therapeutic segments.
The company maintains stringent compliance with global standards and focuses on innovation, quality, and affordability. Mepro’s modern plants support domestic and export markets with a strong emphasis on cGMP, validations, and regulatory excellence.
Known for employee growth, ethical practices, and stability, Mepro offers rewarding long-term careers in one of Gujarat’s prominent pharmaceutical hubs.
Job Details
- Company Name: Mepro Pharmaceuticals Pvt. Ltd. (Unit-III)
- Experience: 2–12 years (varies by role)
- Qualification: B.Sc/M.Sc or B.Pharm/M.Pharm (varies by department)
- Location: Vadodara, Gujarat
- Work Type: On-site
Job Description
Mepro Pharmaceuticals Unit-III, Vadodara is expanding its Quality and Regulatory teams and invites applications from experienced professionals. These roles demand strong GMP knowledge, documentation skills, and compliance expertise in a WHO-GMP environment.
Quality Control – Sr. Executive
- Department: Quality Control
- Role: Sr. Executive
- Experience: 8–10 years
- Education/Qualification: B.Sc / M.Sc (Chemistry / Pharmaceutical Chemistry)
- Key Areas: OOS/OOT investigation, Change Control, Deviation, Incident, CAPA, QMS closure
Quality Control – Asst. Manager
- Department: Quality Control
- Role: Assistant Manager
- Experience: 10–12 years
- Education/Qualification: B.Sc / M.Sc
- Key Areas: Analytical Method Validation/Verification, Tech Transfer, Protocol & Report design, Communication
Quality Control – Officer
- Department: Quality Control
- Role: Officer
- Experience: 2–6 years
- Education/Qualification: B.Sc / M.Sc
- Key Areas: HPLC analysis, RM/PM/In-process/Stability testing, GMP documentation
Regulatory Affairs – Executive / Asst. Manager / Dy. Manager
- Department: Regulatory Affairs
- Role: Executive / Assistant Manager / Deputy Manager
- Experience: 8–12 years
- Education/Qualification: B.Pharm / M.Pharm
- Key Areas: CTD/ACTD/Country-specific dossier submission, CMC assessment, Lifecycle management, ICH tracking
Quality Assurance – Officer / Executive
- Department: Quality Assurance
- Role: Officer / Executive
- Experience: 3–7 years
- Education/Qualification: B.Pharm / M.Pharm
- Key Areas: IPQA, Aseptic monitoring, Validation support, BMR/BPR review, Audits, GMP training
Skills/Qualifications
- Strong hands-on experience in respective QMS/QC/RA activities
- In-depth knowledge of cGMP, ICH, USFDA, WHO guidelines
- Proficiency in HPLC, method validation, dossier compilation
- Excellent documentation and investigation skills
- Good communication and team coordination
- Experience facing regulatory audits preferred
Key Responsibilities
- Handle OOS/OOT/CAPA and QMS elements
- Perform HPLC and stability analysis
- Prepare/submit regulatory dossiers globally
- Conduct IPQA and shop-floor compliance checks
- Lead method validation and tech transfer
- Assess CMC changes and manage lifecycle
- Support internal/external audits and training
Benefits/Perks
- Competitive salary with performance incentives
- Career growth in WHO-GMP facility
- Exposure to global regulatory submissions
- Supportive work culture and training programs
- Job stability with expanding organization
- Vadodara location advantage
How to Apply
Interested candidates should email their updated CV to careers@mepro.in mentioning the Department & Designation in the subject line (e.g., “Application for QC – Sr. Executive”).
For more QC jobs, QA jobs, regulatory affairs openings in Vadodara, and expert guidance, visit Pharma Recruiter.
Apply now – join a company committed to quality and humanity!
Why You Should Join
Mepro Pharmaceuticals offers a professional environment where your expertise directly contributes to patient safety and global healthcare. With strong focus on compliance, innovation, and employee development, Mepro provides excellent long-term career stability.
Work in modern facilities with opportunities to handle high-impact QC, QA, and regulatory projects in a supportive team culture.
FAQs
What experience is required for Regulatory Affairs roles at Mepro Unit-III?
8–12 years in dossier preparation (CTD/ACTD), submission, CMC changes, and lifecycle management.
Is B.Pharm/M.Pharm mandatory for QA positions?
Yes, B.Pharm/M.Pharm with 3–7 years relevant experience in IPQA, validation, and audits.
Are these positions based in Vadodara only?
Yes, all roles are for Mepro Pharmaceuticals Unit-III located in Vadodara, Gujarat.
How to apply for Mepro Pharmaceuticals jobs?
Email CV to careers@mepro.in with department and designation clearly mentioned in subject line.
