Industry
Pharmaceutical Manufacturing & Regulatory Compliance (Formulations & Injectables)
Job Type
Full-Time | Experienced Professionals | GMP-Regulated Environment
Work Location: Vadodara, Gujarat (Unit-III)
About Mepro Pharmaceuticals Pvt. Ltd.
Mepro Pharmaceuticals Pvt. Ltd. is a reputed pharmaceutical manufacturing company known for its strong GMP culture, regulatory compliance, and quality-driven operations. With a robust presence in formulations and injectables, Mepro offers professionals the opportunity to work on regulated markets, critical quality systems, and global dossier submissions from its Vadodara facility (Unit-III). The organization emphasizes data integrity (ALCOA+), continuous improvement, and career growth.
Open Positions – Department Wise
1) Quality Control (QC)
Designations & Experience
- Executive / Senior Executive – 8 to 10 Years
- Officer / Senior Officer – 2 to 6 Years
- Junior Officer – 2 to 4 Years
Qualification: B.Sc / M.Sc
Location: Vadodara, Gujarat
Key Responsibilities
- HPLC, GC, dissolution & stability studies
- RM/PM/FP testing; in-process checks
- Method validation; OOS/OOT investigations
- COA review, analytical data review, calibration
- GMP/GLP compliance & documentation
2) Regulatory Affairs (RA)
Designations & Experience
- Officer – 2 to 6 Years
- Assistant Manager / Deputy Manager – 8 to 12 Years
Qualification: B.Pharm / M.Pharm
Location: Vadodara, Gujarat
Key Responsibilities
- CTD/ACTD dossier preparation & submissions
- African & LATAM market filings
- Regulatory SOPs, lifecycle management
- CMC changes, submission tracking, ICH guidelines
3) Quality Assurance (QA)
Designation: Officer / Senior Officer
Experience: 2 to 6 Years
Qualification: B.Pharm / M.Pharm
Location: Vadodara, Gujarat
Key Responsibilities
- IPQA & AQA activities (OSD, tablets, capsules)
- Line clearance, IPC/CPP monitoring
- BMR/BPR & analytical data review
- Deviations, CAPA, change control
- Stability data review & GMP compliance
Who Can Apply
- Professionals with 2–12 years of pharma experience
- Candidates with QC, QA, or Regulatory Affairs background
- Hands-on exposure to HPLC, GMP, data integrity, CTD dossiers
- B.Sc / M.Sc / B.Pharm / M.Pharm qualified candidates
Why Join Mepro Pharmaceuticals
- Reputed pharma manufacturer with strong compliance culture
- Exposure to injectables & formulations
- Career growth across QC, QA & RA functions
- Professional work environment in Vadodara pharma hub
How to Apply
Online Application (Google Form):
https://docs.google.com/forms/d/e/1FAIpQLSeUS9fuStbeWsCi-3cs6tX_RSB_ecwXBQKXieOICHmALiGviA/viewform?usp=send_form
Alternatively, scan the QR code provided in the official poster.
Interview Preparation Tips
- Revise GMP, GLP, ALCOA+ principles
- Be confident with HPLC, OOS/OOT, validations & audits
- Prepare examples of compliance challenges & resolutions
- Carry updated CV and qualification documents
Frequently Asked Questions (FAQ)
Q1. Which departments are hiring?
Quality Control, Quality Assurance, and Regulatory Affairs.
Q2. What qualifications are required?
B.Sc / M.Sc for QC; B.Pharm / M.Pharm for QA & RA.
Q3. What is the job location?
Vadodara, Gujarat (Unit-III).
Q4. Is experience mandatory?
Yes. Roles require 2 to 12 years based on designation.
Q5. Are freshers eligible?
No, this recruitment is for experienced professionals only.
Q6. What is the selection process?
Profile shortlisting followed by interview(s) as per company process.
Q7. How do I apply?
Apply via the online form or QR code mentioned above.
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Mepro Pharmaceuticals Pvt. Ltd. Hiring Quality Control, Quality Assurance & Regulatory Affairs Professionals
