Mepro Pharmaceuticals Pvt. Ltd., a leading EU-GMP-approved pharmaceutical manufacturer in Vadodara, Gujarat, is expanding its team at Unit-III. With openings in Quality Control jobs in Vadodara, Regulatory Affairs positions in Gujarat pharma, and PPIC roles in pharmaceutical industry, this is an ideal opportunity for experienced professionals seeking career growth in a compliant, innovative environment. Mepro’s commitment to quality and humanity drives its hiring for pharma jobs in Vadodara with 2-12 years experience.
Key Responsibilities by Department
Quality Control (QC) Roles
- Sr. Executive (QMS Section Reviewer): Review and approve QMS documents; ensure compliance with regulatory GDP & GLP requirements in pharmaceutical quality control in Vadodara.
- Asst. Manager: Lead analytical method validation (AMV) using HPLC, GC, UV; review protocols, reports, SOPs; supervise team, method transfers, troubleshooting, and audits under cGMP standards.
- Officer: Perform HPLC analysis for RM/PM testing, in-process, stability samples; maintain strong GMP documentation for QC officer jobs in Gujarat.
Regulatory Affairs (RA) Role
- Senior Position (Team Lead): Review and submit dossiers in CTD, ACTD, country-specific formats; assist in SOPs, system modifications, data management; track ICH guidelines, assess CMC changes, identify risks, propose solutions; lead product milestones and lifecycle compliance in regulatory affairs pharma jobs Vadodara.
PPIC Role
- Officer to Sr. Executive: Forecast inventory, schedule production; raise material orders, coordinate deliveries; liaise with departments for project execution; prepare cost sheets, stock statements; coordinate QA/RA on artwork, vendor qualifications; assist VP Operations in PPIC executive roles in pharmaceutical manufacturing Gujarat.
Qualifications and Experience
- Quality Control: B.Sc/M.Sc in Chemistry/Pharma; 2-6 years (Officer), 8-10 years (Sr. Executive), 10-12 years (Asst. Manager) in QC pharma jobs with HPLC experience.
- Regulatory Affairs: B.Pharm/M.Pharm; 8-12 years in dossier submissions and ICH compliance for senior regulatory affairs team lead Vadodara.
- PPIC: Any Graduate (Pharma experienced preferred); 6-10 years in production planning, inventory management for PPIC jobs in EU-GMP pharma unit.
Benefits at Mepro Pharmaceuticals
Join an EU-GMP-approved facility with competitive salaries, excellent learning opportunities, and clear paths for career development in pharmaceutical industry Vadodara. Work in a reputed setup focused on regulatory compliance, innovation, and employee growth.
How to Apply
Send your updated CV to careers@mepro.in. Use subject line: “[Department] – [Designation] Application” (e.g., “Quality Control – Officer Application”). Only shortlisted candidates will be contacted for Mepro Pharmaceuticals recruitment Vadodara.
FAQs
1. What is the location for these Mepro Pharma jobs in Vadodara?
All positions are based at Mepro Pharmaceuticals Pvt. Ltd. (Unit-III) in Vadodara, Gujarat – an on-site role in a state-of-the-art EU-GMP facility.
2. Is prior pharma experience mandatory for PPIC roles at Mepro?
Yes, 6-10 years with pharma background is preferred for PPIC officer to sr executive jobs in Gujarat, though any graduate with relevant experience may apply.
