Avenza Pharmaceuticals is inviting applications from experienced and aspiring pharmaceutical professionals for multiple openings in the Quality Assurance (QA) Department at its manufacturing facility in Jarod, Samlaya, Vadodara. Candidates with B.Pharm or M.Pharm qualifications and experience in IPQA, QMS, Qualification & Validation, Documentation Control, and Analytical QA are encouraged to apply.
This is an excellent opportunity for pharma professionals looking to build a rewarding career in regulated market operations, compliance, and pharmaceutical quality systems.
Author: pharmabharat editorial team
Avenza Pharmaceuticals QA Vacancy Details
| Section | No. of Positions | Experience Required |
|---|---|---|
| IPQA | 5 | 1–5 Years |
| IPQA | 1 | 8–10 Years |
| Documentation Issuance & Control | 1 | 0–2 Years |
| Qualification & Validation | 1 | 4–6 Years |
| QMS | 1 | 5–7 Years |
| Analytical QA | 1 | 4–6 Years |
Qualification
- B.Pharm
- M.Pharm
Job Location
- Jarod, Samlaya, Vadodara, Gujarat
Key Responsibilities
IPQA & Shop Floor Monitoring
- Monitoring manufacturing and shop floor activities
- Handling granulation, compression, coating, encapsulation, and packing processes
- Ensuring compliance with GMP guidelines
- Managing in-process quality assurance activities
Serialization & Track and Trace
- Handling EU FMD Serialization systems
- Maintaining track and trace compliance for regulated markets
Documentation Control
- Documentation issuance and control management
- Maintaining SOPs, logbooks, and controlled documents
- Ensuring documentation compliance as per QA standards
Qualification & Validation
- Process validation activities
- Cleaning validation
- Vendor qualification
- Facility and equipment qualification
QMS Activities
- Managing Change Control, Deviation, and CAPA systems
- Supporting audits and compliance initiatives
- Maintaining pharmaceutical quality systems
Analytical QA
- Analytical document review
- Audit trail review
- Compliance review of analytical data
Required Skills
- Strong understanding of pharmaceutical QA systems
- Knowledge of GMP/GLP guidelines
- Experience in regulated market compliance
- Good communication and documentation skills
- Team-oriented mindset with attention to detail
Why Join Avenza Pharmaceuticals?
- Work in a dynamic and compliant pharmaceutical environment
- Excellent learning and career growth opportunities
- Exposure to regulated market operations
- Opportunity to work with experienced QA professionals
- Quality-driven work culture focused on integrity and innovation
How to Apply
Interested candidates can send their updated resume to:
Email: recruitment@avenzapharma.com
