Pharmazone is expanding its team and inviting applications from experienced professionals across Business Development, GMP Quality Assurance, Engineering Qualification, Clinical Research, and Pharmacovigilance. If you are seeking pharma jobs in India, especially in GMP QA roles, Clinical Research Associate jobs, Pharmacovigilance aggregate report jobs, or engineering qualification roles in pharma, this is an excellent opportunity to advance your career.
This latest Pharmazone hiring notification is ideal for candidates with experience in OSD, sterile manufacturing, BA-BE studies, RMP, PSUR, PADER, and equipment qualification.
Open Positions at Pharmazone
1️⃣ Business Development Executive (Pharma Services)
Experience: 2+ years
Domain: Pharma services sales
Key Responsibilities:
- Identify and generate leads for pharma consulting and compliance services
- Develop client relationships in GMP, QA, regulatory, and clinical segments
- Prepare proposals and close B2B pharma service contracts
- Coordinate with internal technical teams for service execution
Qualifications:
- Bachelor’s or Master’s degree in Pharmacy/Life Sciences/MBA
- 2+ years experience in selling pharma services
- Strong communication and negotiation skills
2️⃣ GMP – QA Expert (OSD & Sterile Manufacturing)
Experience: 10+ years
Key Responsibilities:
- Lead GMP compliance for OSD and sterile manufacturing sites
- Oversee CQA implementation and regulatory readiness
- Conduct internal audits and CAPA management
- Support inspections (CDSCO, USFDA, MHRA, WHO-GMP)
Qualifications:
- B.Pharm / M.Pharm / Life Sciences
- 10+ years in Quality Assurance / CQA
- Strong expertise in OSD and sterile manufacturing operations
3️⃣ GMP – Engineering Expert (Qualification)
Experience: 5+ years
Key Responsibilities:
- Qualification of utilities and production equipment
- IQ, OQ, PQ documentation and validation
- HVAC, water systems, cleanroom qualification
- Ensure regulatory compliance with GMP standards
Qualifications:
- B.E/B.Tech in Mechanical/Electrical/Instrumentation
- 5+ years in pharma equipment and utility qualification
- Experience in sterile/OSD facility setup preferred
4️⃣ Clinical Research Associate (BA-BE Studies)
Experience: 1+ year
Key Responsibilities:
- Monitor BA-BE clinical trials as per GCP guidelines
- Site management and documentation review
- Coordinate with investigators and ethics committees
- Ensure regulatory compliance and audit readiness
Qualifications:
- B.Pharm / M.Pharm / Pharm.D / Life Sciences
- 1+ year experience in BA-BE studies
- Knowledge of ICH-GCP
5️⃣ Pharmacovigilance – Aggregate Report Specialist
Experience: 4+ years
Key Responsibilities:
- Prepare and review RMP, PSUR, PADER reports
- Signal detection and benefit-risk evaluation
- Ensure global PV compliance
- Support regulatory submissions
Qualifications:
- B.Pharm / M.Pharm / Pharm.D / Life Sciences
- 4+ years experience in aggregate reporting
- Strong understanding of global pharmacovigilance guidelines
Salary & Benefits
- Competitive salary packages based on experience
- CRA: ₹3.5 – ₹6 LPA
- PV Specialist: ₹6 – ₹12 LPA
- QA Expert: ₹12 – ₹22 LPA
- Engineering Expert: ₹6 – ₹14 LPA
- Business Development: ₹4 – ₹8 LPA
- Exposure to GMP consulting and regulatory projects
- Career growth in pharma compliance and clinical domains
- Professional work environment
How to Apply
Interested candidates can send their updated resume to:
📧 hr@pharmazones.com
Subject Line: Application for [Position Name]
