Intas Pharmaceuticals, one of the world’s leading pharmaceutical companies, is inviting applications for Executive / Sr. Executive – Validation & Qualification (QA) roles at its Matoda, Ahmedabad facility.
If you’re a motivated QA professional with a strong foundation in validation, qualification, and regulatory compliance, this is your opportunity to join a globally recognized pharmaceutical organization driving innovation and quality.
Key Responsibilities
- Develop, execute, and document qualification and validation protocols for equipment, utilities, and facilities in a regulated pharma setup (OSD/Injectable).
- Ensure compliance with USFDA, WHO-GMP, MHRA, and other global regulatory standards.
- Manage QMS, CAPA, validation documentation, and audit readiness.
- Collaborate with Engineering, Manufacturing, and Quality Control teams for validation integrity and data compliance.
- Apply strong knowledge of cGMP, GxP, and data integrity (ALCOA+) principles.
- Ensure adherence to 21 CFR Part 11 for electronic records, audit trails, and system qualification.
Qualifications & Experience
- B. Pharmacy / M. Pharmacy / M.Sc / B.Tech / B.E.
- 4–10 years of hands-on experience in equipment, utility, and facility qualification within a regulated pharmaceutical manufacturing environment.
- Strong technical expertise in QA validation processes and regulatory audits.
- Excellent documentation and cross-functional communication skills.
Why Join Intas?
- Work with a global pharmaceutical leader shaping the future of healthcare.
- Exposure to international regulatory standards and advanced quality systems.
- Competitive salary and comprehensive employee benefits.
- Opportunity to grow in a progressive, innovation-driven environment.
Job Location
📍 Matoda, Ahmedabad, Gujarat, India
How to Apply
Interested candidates can share their updated CV at
📧 krisha_prajapati@intaspharma.com
Mention “Profile for Validation & Qualification (QA)” in the subject line.
🕓 Apply before: [Automatically closes 30 days from posting]
FAQs
1. What is the experience requirement for this role?
Candidates should have 4–10 years of experience in validation and qualification within a regulated pharma setup.
2. Where is this position located?
The role is based at Intas Pharmaceuticals’ Matoda facility in Ahmedabad, Gujarat.
