Intas Pharmaceuticals Hiring for Validation / Qualification (QA) roles at its Matoda, Ahmedabad facility.
Intas Pharmaceuticals, a global leader in the pharmaceutical industry, has announced exciting job openings for Executive / Senior Executive – Validation & Qualification (QA) positions at its Matoda, Ahmedabad facility. This recruitment is a great opportunity for experienced professionals in Quality Assurance (QA) to work with one of India’s most trusted and internationally recognized pharmaceutical organizations. Intas Pharmaceuticals Hiring for Validation / Qualification
If you have hands-on experience in equipment qualification, process validation, and regulatory compliance, this role offers a dynamic work environment and career advancement in a globally regulated setup. Below are the complete details of this opportunity, including responsibilities, eligibility, skills required, and how to apply. Intas Pharmaceuticals Hiring for Validation / Qualification
About Intas Pharmaceuticals Ltd
Intas Pharmaceuticals Ltd is one of India’s fastest-growing multinational pharmaceutical companies, known for its commitment to innovation, research, and global healthcare standards. Headquartered in Ahmedabad, Gujarat, Intas operates across 85+ countries, with strong presence in regulated markets such as the United States, United Kingdom, and European Union. Intas Pharmaceuticals Hiring for Validation / Qualification
The company specializes in formulations development, manufacturing, and marketing of a wide range of therapeutic products, including oncology, neurology, cardiovascular, and biosimilars. With world-class facilities approved by international regulatory bodies like USFDA, MHRA, EMA, and WHO-GMP, Intas continues to set benchmarks in pharmaceutical excellence.
At Intas, employees are encouraged to pursue continuous learning, innovation, and teamwork — making it an ideal workplace for professionals seeking long-term career growth in the pharmaceutical quality and validation domain. Intas Pharmaceuticals Hiring for Validation / Qualification
Job Overview: Validation & Qualification (QA)
Position: Executive / Sr. Executive – Validation & Qualification (QA)
Department: Quality Assurance (QA)
Location: Matoda, Ahmedabad, Gujarat, India
Experience Required: 4 to 10 years
Qualification: B.Pharmacy, M.Pharmacy, M.Sc, B.Tech, or B.E
Employment Type: Full-time (On-site)
Industry: Pharmaceutical Manufacturing
This position is suitable for professionals experienced in equipment, utility, and facility qualification in regulated manufacturing setups (OSD or Injectable). Candidates should have strong expertise in quality systems, compliance documentation, and process validation. Intas Pharmaceuticals Hiring for Validation / Qualification
Key Responsibilities
As part of the Validation & Qualification QA Team at Intas Pharmaceuticals, you will play a vital role in ensuring that manufacturing and support systems comply with global quality and regulatory standards. Intas Pharmaceuticals Hiring for Validation / Qualification
Your primary responsibilities will include:
- Developing, executing, and maintaining qualification and validation protocols for production equipment, utilities, and facilities.
- Preparing and reviewing IQ (Installation Qualification), OQ (Operational Qualification), and PQ (Performance Qualification) documents.
- Ensuring compliance with USFDA, MHRA, WHO-GMP, and other international regulatory requirements.
- Managing Quality Management System (QMS) activities related to validation, including CAPA, deviations, and audit readiness.
- Collaborating with Engineering, Manufacturing, and QC teams to ensure equipment qualification integrity and alignment with validation master plans.
- Applying strong understanding of cGMP, GxP, and ALCOA+ (data integrity) principles in all documentation and activities.
- Ensuring compliance with 21 CFR Part 11 for electronic systems, audit trails, and computerized equipment qualification.
- Participating in internal and external audits, and providing necessary support documentation to regulatory authorities.
- Maintaining Validation Master Plans (VMP) and ensuring timely requalification and revalidation of equipment and systems.
This role demands meticulous attention to detail, strong technical knowledge, and the ability to work collaboratively across cross-functional teams. Intas Pharmaceuticals Hiring for Validation / Qualification
Required Qualifications and Experience
Educational Qualification:
- B.Pharmacy / M.Pharmacy
- M.Sc in Chemistry or related discipline
- B.Tech / B.E in Chemical, Mechanical, or related engineering fields
Experience:
- Minimum 4 to 10 years of experience in validation and qualification within a regulated pharmaceutical environment (OSD/Injectable preferred).
- Hands-on experience in equipment qualification, utility validation, and facility qualification.
- Exposure to regulatory audits (USFDA, MHRA, WHO, or EU).
- Proficiency in preparing validation documentation, risk assessments, and change control reports.
Technical Skills:
- Strong command of GMP and GxP principles.
- In-depth knowledge of validation lifecycle management.
- Familiarity with CSV (Computer System Validation) concepts.
- Expertise in using quality and document management systems.
- Excellent communication and coordination abilities.
Why Join Intas Pharmaceuticals?
Working at Intas Pharmaceuticals Ltd means being part of a world-class organization that values innovation, ethics, and excellence. The company offers not only a competitive salary but also a collaborative and growth-oriented culture. Intas Pharmaceuticals Hiring for Validation / Qualification
Key benefits of working at Intas include:
- Exposure to global regulatory environments such as USFDA, MHRA, and WHO-GMP.
- Opportunities to work on advanced quality systems and validation technologies.
- Continuous learning and development through structured training programs.
- Career growth and promotion opportunities in a multinational setup.
- Competitive salary structure and performance-linked incentives.
- Comprehensive employee welfare programs including health insurance and other benefits.
Intas provides an inclusive and professional workplace where QA professionals can refine their expertise and progress toward leadership roles in quality and validation.
Job Location
Matoda, Ahmedabad, Gujarat, India
The Matoda manufacturing facility of Intas Pharmaceuticals is one of the company’s largest production units, designed with state-of-the-art infrastructure and world-class laboratories. It is located near Ahmedabad city and well-connected by road and public transport. Intas Pharmaceuticals Hiring for Validation / Qualification
How to Apply
Interested candidates who meet the eligibility criteria can apply for the Validation & Qualification (QA) position by sharing their resume with the HR department via email.
Email ID:
📧 krisha_prajapati@intaspharma.com
Subject Line:
“Profile for Validation & Qualification (QA) – [Your Name]”
Applicants should ensure their resumes highlight relevant experience in validation, qualification, and regulatory compliance. Include details about handled equipment, audit exposure, and process expertise to strengthen your application. Intas Pharmaceuticals Hiring for Validation / Qualification
Application Deadline:
Applications are open for 30 days from the posting date (October 29, 2025).
Important Tips Before Applying
To enhance your chances of selection, consider the following points before applying:
- Review your resume to include key skills such as validation, qualification, QMS, and regulatory audits.
- Prepare for technical discussions on IQ, OQ, PQ, CSV, and data integrity principles.
- Familiarize yourself with Intas’s product lines and regulatory scope.
- Ensure you have experience certificates, educational documents, and ID proofs ready for verification.
- Maintain professionalism and punctuality during any interview or technical discussion.
This role is ideal for professionals who aspire to grow in a high-performance, quality-driven environment and contribute to maintaining global pharmaceutical standards.
FAQs
Q1. What is the required experience for this role at Intas Pharmaceuticals?
Candidates should have 4 to 10 years of experience in validation and qualification within a regulated pharmaceutical manufacturing setup.
Q2. What qualifications are accepted for this position?
Applicants with B.Pharmacy, M.Pharmacy, M.Sc, B.Tech, or B.E degrees are eligible.
Q3. Where is the job located?
The position is based at Matoda, Ahmedabad, Gujarat, one of Intas Pharmaceuticals’ major manufacturing facilities.
Q4. What type of work environment does Intas offer?
Intas provides a globally compliant, professional, and growth-oriented workplace with opportunities for skill enhancement and cross-functional exposure.
Q5. How can I apply?
Interested candidates should send their CVs to krisha_prajapati@intaspharma.com with the subject line “Profile for Validation & Qualification (QA).”
Conclusion
The Validation & Qualification (QA) openings at Intas Pharmaceuticals present a valuable opportunity for professionals with experience in quality assurance and validation processes. With its world-class manufacturing standards, exposure to international audits, and emphasis on professional development, Intas offers one of the most rewarding career paths in the pharmaceutical industry. Intas Pharmaceuticals Hiring for Validation / Qualification
If you have 4–10 years of experience in equipment qualification, process validation, or regulatory QA, and are looking to join a global leader known for excellence, this is your chance. Intas Pharmaceuticals Hiring for Validation / Qualification
Apply now and take the next big step in your pharmaceutical career with Intas Pharmaceuticals, Matoda, Ahmedabad.
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Note: This job information is sourced from publicly available official sources. We share it for reference purposes only and do not claim ownership of the job posting.
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