Avenza Pharma Announces Major Recruitment Initiative for Experienced Professionals in Quality Assurance, Quality Control, and Analytical R&D at Vadodara Facility
Pharm'Up 
Avenza Pharma has officially announced a significant recruitment drive aimed at hiring experienced professionals for its comprehensive pharmaceutical manufacturing and Research & Development (R&D) campus located in Jarod, Samlaya, Vadodara, Gujarat, India.
The company operates a state-of-the-art manufacturing unit integrated with sales and R&D, supported by an ultra-advanced analytical laboratory system. All facilities strictly comply with global regulatory and safety standards, including requirements for regulated markets such as the USFDA, MHRA, TGA, and EU-GMP.
Avenza is currently seeking qualified candidates for the following departments and positions:
1. Quality Control (QC) Department
- Experience Required: 3–5 years.
- Open Positions:
- QC QMS
- QC Documentation
- QC Reviewer
- HPLC/GC
- Key Requirements: Candidates must possess relevant pharmaceutical industry experience (3–5 years), a robust understanding of applicable regulations, Standard Operating Procedures (SOPs), and Current Good Manufacturing Practices (cGMP). Excellent communication and documentation skills are essential, along with the ability to work effectively within a team and meet strict deadlines.
2. QC Micro (Microbiology) Department
- Experience Required: 2–3 years.
- Open Position:
- QC Micro.
- Key Requirements: Applicants are required to have expertise in the microbiological analysis of raw materials, packaging materials, in-process samples, and finished products. Responsibilities will include environmental monitoring, microbial limit testing, media preparation, and sterility testing. Strong documentation skills, along with experience in investigation and deviation handling, are mandatory. Candidates must demonstrate full compliance with cGMP, SOPs, and regulatory requirements.
3. Quality Assurance (QA) Department
- Experience Required: 3–5 years.
- Open Position:
- QA – IPQA (3 positions available).
- Key Requirements: This role requires specific experience in regulated-market operations (USFDA, MHRA, TGA, or EU-GMP). Candidates must have a deep knowledge of applicable regulations, SOPs, and cGMP. Strong communication and documentation skills are critical, as is the ability to function well in a team environment and adhere to deadlines.
4. Analytical Research & Development (AR&D) Department
- Experience Required: 3–5 years.
- Open Position:
- Analytical Research & Development.
- Key Requirements: The primary focus will be analytical development and validation for Oral Solid Dosage (OSD) formulations. Candidates must have strong exposure to method development, method validation, AMV/ICH guidelines, troubleshooting, and regulatory support.
Application Instructions
Interested and eligible candidates are invited to apply by sending their updated resume to:
Email: recruitment@avenzapharma.com
Subject Line: Application for [Please specify the department: QC / QC Micro / QA / AR&D]
Mandatory Email Details: To ensure the application is processed correctly, applicants must mention the following details clearly in the body of the email:
- Total Experience
- Current CTC (Cost to Company)
- Expected CTC
- Notice Period
Job Location: Jarod, Samlaya, Vadodara, Gujarat.
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