Pharmazone Hiring For Regulatory Affairs / Quality Control / Quality Assurance / Business Development
Pharmazone has announced a major walk-in recruitment drive for experienced pharma professionals in Regulatory Affairs, Quality Assurance, Quality Control, GMP, and Business Development divisions.
Candidates with experience in USFDA, MHRA, EU-GMP, OSD Formulations, Regulatory Submissions, Pharma Consulting, and Biotech Projects are encouraged to attend the walk-in interview.
📋 Walk-In Interview Details
🏢 Company: Pharmazone
📍 Location: Ahmedabad, Gujarat, India
📅 Interview Date 1:
21 May 2026 (Thursday)
⏰ Timing:
06:00 PM – 10:00 PM
📅 Interview Date 2:
24 May 2026 (Sunday)
⏰ Timing:
09:30 AM – 12:30 PM
💼 Industry:
Regulatory Affairs / GMP / Pharma Consulting
🧑💻 Experience Required:
2–10 Years
Pharmazone Ahmedabad Office
Ahmedabad, Gujarat, India
- Updated Resume/CV
- Educational Documents
- Experience Certificates
- Government Photo ID Proof
📌 Available Open Positions
| Department | Role | Experience | Qualification | Vacancies |
|---|---|---|---|---|
| GMP | Quality Assurance (Formulation) | 8–10 Years | B.Pharm / M.Pharm | 2 |
| GMP | Quality Control (Formulation) | 8–10 Years | M.Sc / B.Pharm / M.Pharm | 2 |
| GMP | Project Manager | 6–10 Years | B.Pharm / M.Pharm / M.Sc | 2 |
| Business Development | BD Executive | 2 Years | B.Sc / M.Sc | 1 |
| Regulatory Affairs | Regulatory Affairs Executive | 2–5 Years | B.Pharm / M.Pharm | 2 |
| Regulatory Affairs | Project Manager (F&D/Micro) | 2–5 Years | B.Pharm / M.Pharm | 1 |
| Regulatory Affairs | Project Manager (Biotech APAC/EU) | 2–5 Years | B.Pharm / M.Pharm | 1 |
📌 Key Responsibilities
🧪 Quality Assurance & Quality Control
- Handle GMP documentation and compliance activities
- Support USFDA, MHRA, and EU-GMP compliance requirements
- Conduct audits, investigations, and validation activities
- Manage OSD formulation quality systems
- Ensure inspection readiness and regulatory compliance
📑 Regulatory Affairs
- Prepare and review regulatory dossiers
- Handle submissions for US, EU, APAC, and global markets
- Manage lifecycle maintenance and approvals
- Coordinate with pharma and biotech cross-functional teams
- Support registration and regulatory documentation
💼 Business Development
- Promote pharma consulting services
- Build relationships with pharma and biotech clients
- Generate new business opportunities
- Support company growth initiatives
🎓 Eligibility Criteria
- B.Pharm
- M.Pharm
- M.Sc
- B.Sc (For Business Development Role)
⭐ Preferred Skills
- OSD Formulation Experience
- Knowledge of USFDA, MHRA & EU-GMP Regulations
- Regulatory Affairs Expertise
- Biotech APAC/EU Exposure
- Project Management Skills
- Strong Communication Abilities
🌍 Why Join Pharmazone?
- Exposure to global pharma regulatory markets
- Career growth in Regulatory Affairs & GMP
- Opportunity to work with biotech and pharma leaders
- Professional development in pharma consulting
- Dynamic and collaborative work environment
📄 Resume Tips
- Highlight regulatory submission experience clearly
- Mention QA/QC and GMP expertise
- Add audit and inspection handling experience
- Use ATS-friendly formatting
- Keep resume concise and professional
- Showcase leadership and communication skills
🧩 Fun Learning & Career Growth
🚀 Apply Now
📩 Send Updated CV To:
hr@pharmazones.com
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