Avenza Hiring QA IPQA, AR&D & QC
- Company Overview
- Job Role & Responsibilities
- Quality Assurance – IPQA
- Analytical R&D (AR&D)
- Quality Control – Reviewer & QMS
- Eligibility / Qualifications
- Required Education
- Experience Requirements
- Additional Requirements
- Location & Salary
- Location:
- Salary:
- Application Process
- Why This Opportunity Stands Out
- FAQs
- Who can apply for these roles?
- What departments are hiring?
- Is experience mandatory?
- Are freshers eligible?
- How to apply?
- Summary Table
Avenza Pharma Hiring QA IPQA, AR&D & QC Roles – Pharma Jobs in Vadodara with Immediate Joiners Preferred
Avenza Pharmaceuticals Private Limited has announced multiple openings across Quality Assurance (IPQA), Analytical Research & Development (AR&D), and Quality Control (QC – Reviewer & QMS) departments at its Jarod, Vadodara facility. The company is hiring professionals with 1 to 9 years of experience depending on the role, making this a strong opportunity for both early-career and experienced candidates in pharmaceutical quality and research domains.
These vacancies include QA IPQA roles for candidates with 1–3 years of experience, AR&D positions for 2–6 years experienced professionals, and senior QC Reviewer/QMS roles for candidates with 5–9 years of experience. Candidates with B.Pharm, M.Pharm, B.Sc, and M.Sc qualifications are eligible based on department requirements. Immediate joiners are preferred, making this a time-sensitive opportunity.
Company Overview
Avenza Pharmaceuticals Private Limited is a growing pharmaceutical company focused on delivering high-quality formulations while maintaining strong compliance with regulatory standards. The company operates with a commitment to quality assurance, analytical excellence, and continuous improvement in manufacturing and research processes.
The Vadodara facility supports pharmaceutical manufacturing and analytical operations, ensuring adherence to global standards. Companies like Avenza play a vital role in ensuring product safety, regulatory compliance, and consistent quality in the pharmaceutical supply chain.
Working at Avenza offers exposure to:
- Pharmaceutical quality systems and regulatory compliance
- Analytical research and method development processes
- Cross-functional collaboration across QA, QC, and R&D
- Audit readiness and documentation practices
This environment is ideal for professionals looking to grow in pharma quality assurance, analytical research, and regulatory domains.
Job Role & Responsibilities
Quality Assurance – IPQA
- Perform in-process quality checks during manufacturing
- Ensure compliance with cGMP guidelines and SOPs
- Monitor production activities and maintain documentation
- Handle deviations, CAPA, and quality investigations
Analytical R&D (AR&D)
- Support analytical method development and validation
- Perform sample analysis and data interpretation
- Handle laboratory instruments and maintain records
- Assist in stability studies and analytical documentation
Quality Control – Reviewer & QMS
- Review analytical data and laboratory documentation
- Ensure compliance with QMS and regulatory guidelines
- Handle audit documentation and quality systems
- Support investigations, deviations, and change control
These roles are essential in maintaining pharmaceutical product quality, ensuring regulatory compliance, and supporting research and development processes.
Eligibility / Qualifications
Required Education
Candidates must have relevant pharmaceutical or science qualifications.
Accepted courses include:
B.Pharm, M.Pharm, B.Sc, M.Sc, Pharmaceutical Sciences, Chemistry, Life Sciences, Biotechnology
Experience Requirements
- QA IPQA: 1–3 years
- AR&D: 2–6 years
- QC Reviewer/QMS: 5–9 years
Additional Requirements
- Experience in pharmaceutical or regulated environments preferred
- Strong knowledge of cGMP and documentation practices
- Immediate joiners preferred
Location & Salary
Location:
- Jarod, Vadodara, Gujarat
Salary:
- Salary is not disclosed
- Roles in QA, QC, and AR&D typically offer strong career growth and competitive compensation in pharma industry
Application Process
Interested candidates can apply by sending their resume to:
Candidates are advised to:
- Clearly mention department and role in subject line
- Highlight relevant experience in QA, QC, or AR&D
- Ensure resume includes regulatory and technical skills
Why This Opportunity Stands Out
- Multiple openings across QA, QC, and AR&D departments
- Opportunity to work in regulated pharmaceutical environment
- Strong career growth in quality assurance and research domains
- Preference for immediate joiners increases selection chances
This hiring drive is ideal for professionals aiming to build or advance careers in pharmaceutical quality systems, analytical research, and regulatory compliance.
FAQs
Who can apply for these roles?
Candidates with B.Pharm, M.Pharm, B.Sc, or M.Sc qualifications and relevant experience can apply.
What departments are hiring?
Quality Assurance (IPQA), Analytical R&D, and Quality Control (Reviewer/QMS).
Is experience mandatory?
Yes, experience ranging from 1 to 9 years is required depending on the role.
Are freshers eligible?
No, these roles require prior experience in pharmaceutical domains.
How to apply?
Candidates can send their resume to the provided email ID.
Summary Table
| Company | Avenza Pharmaceuticals Private Limited |
|---|---|
| Vacancies | QA IPQA, AR&D, QC Reviewer/QMS |
| Required Education | B.Pharm, M.Pharm, B.Sc, M.Sc, Life Sciences, Chemistry |
| Experience | 1–9 years depending on role |
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