Avenza Pharmaceuticals Hiring For Quality Assurance

Avenza Pharmaceuticals Pvt Ltd has announced new Quality Assurance jobs in Vadodara for experienced pharmaceutical professionals. The company is recruiting for QA-IPQA and Qualification & Validation positions at its HPRA-approved plant located at Jarod, Samlaya, Vadodara, Gujarat.

This Avenza Pharmaceuticals recruitment drive offers opportunities for professionals with 2 to 5 years of relevant pharmaceutical industry experience in IPQA, qualification, validation, documentation, deviation handling and regulatory compliance.

Candidates looking for pharma QA jobs in Vadodara, IPQA jobs in Gujarat, or pharmaceutical validation jobs can review the eligibility and application details below.

Avenza Pharmaceuticals Vacancy Overview

1. QA-IPQA – 3 Vacancies

Experience Required: 2–4 years

The QA-IPQA role focuses on maintaining quality and GMP compliance during pharmaceutical manufacturing operations.

Key Responsibilities

• Perform in-process quality assurance activities.
• Conduct line clearance before manufacturing and packaging operations.
• Perform and document in-process checks.
• Maintain accurate IPQA documentation and records.
• Prepare IPQA reports.
• Support deviation identification, documentation and handling.
• Ensure manufacturing activities are performed according to approved procedures and applicable quality requirements.

2. Qualification & Validation – 1 Vacancy

Experience Required: 4–5 years

This Quality Assurance position focuses on pharmaceutical equipment, utilities, systems and process qualification and validation.

Key Responsibilities

• Perform equipment and utilities qualification activities.
• Handle process qualification and validation.
• Conduct validation of equipment, systems and manufacturing processes.
• Support cleaning validation activities.
• Prepare qualification and validation protocols.
• Review and finalize validation reports and associated documentation.
• Maintain documentation in accordance with applicable regulatory requirements.
• Ensure qualification and validation activities comply with pharmaceutical quality standards.

Qualification & Eligibility

The employer advertisement specifies the required experience but does not explicitly mention an educational qualification.

Based on the nature of pharmaceutical Quality Assurance, IPQA, qualification and validation functions, candidates commonly considered for similar positions may hold:

• B.Pharm
• M.Pharm
• B.Sc in a relevant science discipline
• M.Sc in a relevant science discipline

Important: These degrees are editorial guidance and are not explicitly listed in the Avenza Pharmaceuticals recruitment notice. Candidates should confirm their educational eligibility directly with the employer before applying.

For QA-IPQA, applicants should have approximately 2–4 years of relevant experience. Candidates applying for Qualification & Validation should have approximately 4–5 years of relevant experience.

Key Skills

Relevant skills for these Avenza Pharmaceuticals QA jobs include IPQA, line clearance, in-process quality checks, GMP documentation, deviation handling, equipment qualification, utility qualification, process validation, cleaning validation, validation protocols, validation reports and regulatory compliance.

Why Consider This Opportunity?

The recruitment is for Avenza Pharmaceuticals’ HPRA-approved plant, providing experienced QA professionals an opportunity to work in a regulated pharmaceutical manufacturing environment.

The positions provide exposure to important Quality Assurance functions including shop-floor IPQA, documentation, deviation management, equipment and utility qualification, process validation and cleaning validation.

Note: The employer advertisement does not specify salary, employee benefits, incentives or other compensation details. Candidates should discuss these directly during the recruitment process.

How to Apply for Avenza Pharmaceuticals Jobs

Interested candidates should send an updated resume to:

Email: recruitment@avenzapharma.com