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Kickstart or elevate your career in the pharmaceutical industry!
Avenza Pharmaceuticals Pvt Ltd, a leader in Oral Solid Dosage (OSD) formulation, is conducting a walk-in interview for multiple roles at its Vadodara facility. This is a golden opportunity to join a company with exposure to regulated markets like USFDA, MHRA, TGA, EU-GMP, etc.
Walk-In Interview Details
- 📅 Date: 26th July 2025 (Saturday)
- 🕘 Time: 10:00 AM to 4:00 PM
- 🏢 Venue:
Avenza Pharmaceuticals Pvt Ltd
Unit 111/1, Jarod- Samlaya Road,
At. Vadadala, Tal. Savli,
Dist. Vadodara – 391520, Gujarat
Current Openings
Quality Control (QC)
- GLP compliance
- HPLC analysis
- QMS support
- QC Analysts
Quality Assurance (QA)
- QMS documentation
- Training & compliance
- Computer System Validation (CSV)
Warehouse
- 2–5 years of experience (Pharma industry)
- cGMP knowledge
- Material handling & ERP documentation
Apprenticeship Program – 1 Year
- Open to freshers from B.Sc, M.Sc, B.Pharm, M.Pharm
- Ideal platform to enter pharma manufacturing
✅ Candidate Profile
- Background in OSD formulation preferred
- Strong skills in documentation & regulatory compliance
- Immediate joiners will be given preference
- Fresh graduates eligible for apprenticeship
📄 Documents to Carry
- Updated CV
- Passport-size photo
- Educational & experience certificates
- Last 3 months’ salary slips
- Current CTC structure
📧 Send Your Resume/Queries
💡Sample Interview Questions & Answers
Q1: What is the difference between QA and QC?
A: QA is process-oriented and focuses on preventing defects, while QC is product-oriented and detects defects in finished products.
Q2: What is HPLC used for in pharma QC?
A: HPLC (High-Performance Liquid Chromatography) is used to separate, identify, and quantify compounds in pharmaceutical formulations.
Q3: What are cGMP guidelines?
A: cGMP (current Good Manufacturing Practices) are regulatory standards for ensuring product quality, safety, and consistency in pharma manufacturing.
Q4: What is the importance of QMS?
A: QMS (Quality Management System) helps ensure consistent product quality, compliance with regulations, and continuous improvement.
Q5: What is CSV in QA?
A: CSV (Computer System Validation) ensures software and hardware systems in pharma perform consistently as intended and comply with regulations.
📢 Why Join Avenza Pharmaceuticals?
- Exposure to global regulatory markets (USFDA, MHRA, etc.)
- Strong mentorship and career growth
- Hands-on experience in modern pharma processes
- Structured apprenticeship for freshers
