Intas Pharmaceuticals Walk-In Drive for QA, QC & Microbiology Professionals at Matoda, Ahmedabad

Intas Pharmaceuticals Ltd., one of the world’s leading multinational pharmaceutical companies, has announced a Walk-In Interview Drive for experienced professionals in Quality Assurance, Quality Control, and Microbiology at its Matoda manufacturing facility in Ahmedabad, Gujarat. This recruitment drive offers an excellent opportunity for candidates seeking career growth in a globally recognized pharmaceutical organization with a strong presence in over 85 countries.

Intas continues to expand its operations in regulated markets including the US and Europe, making it an attractive employer for pharmaceutical professionals looking to work in a high-quality manufacturing environment.

About Intas Pharmaceuticals

Intas Pharmaceuticals is a leading pharmaceutical formulation development, manufacturing, and marketing company. The organization derives a significant portion of its revenue from international regulated markets and is known for maintaining high standards of quality, compliance, and innovation.

Walk-In Interview Details

Interview Date: 21st June 2026 (Sunday)

Time: 09:30 AM to 03:00 PM

Venue: Intas Pharmaceuticals Ltd., Matoda Facility, Ahmedabad, Gujarat

Available Positions

1. Quality Assurance (QMS / Analytical Review / Validation / IPQA – Parenteral & OSD)

Designation: Officer / Senior Officer / Executive

Qualification:

B.Pharm

M.Pharm

M.Sc

Experience Required:

2 to 7 Years

2. Quality Control

Designation: Senior Officer / Executive

Qualification:

B.Sc / M.Sc (Organic Chemistry / Analytical Chemistry)

B.Pharm

M.Pharm

Experience Required:

3 to 7 Years

3. Microbiology

Designation: Senior Officer / Executive

Qualification:

B.Sc / M.Sc (Microbiology)

Experience Required:

3 to 7 Years

Candidate Requirements

Applicants should possess:

Strong knowledge of cGMP guidelines.

Understanding of laboratory safety practices.

Experience in regulated pharmaceutical facilities.

Relevant functional expertise in their respective departments.

Good documentation and compliance knowledge.

Documents to Carry

Candidates are advised to bring:

Updated Resume/CV

Educational Certificates

Experience Certificates

Current Salary Documents

Recent Passport-size Photographs

Note: Candidates who have attended an interview with Intas Pharmaceuticals within the last six months are requested not to apply.

Why Join Intas Pharmaceuticals?

Opportunity to work with a globally recognized pharmaceutical company.

Exposure to regulated markets including USFDA and EU-GMP environments.

Career growth and learning opportunities.

Competitive compensation and professional development programs.

Modern manufacturing facilities and quality-driven culture.

Technical FAQs

1. What is IPQA and why is it important in pharmaceutical manufacturing?

IPQA (In-Process Quality Assurance) ensures that manufacturing activities comply with approved procedures and GMP requirements during production. It helps maintain product quality, consistency, and regulatory compliance.

2. What are the key responsibilities of a Quality Control executive?

A QC executive performs raw material, in-process, and finished product testing, maintains laboratory documentation, operates analytical instruments such as HPLC and GC, and ensures compliance with regulatory requirements.

3. What is Analytical Method Validation?

Analytical Method Validation is the documented process of proving that an analytical procedure is suitable for its intended purpose. Parameters include accuracy, precision, specificity, linearity, robustness, and detection limits.

4. What microbiological tests are commonly performed in pharmaceutical industries?

Common tests include microbial limit testing, sterility testing, environmental monitoring, water testing, endotoxin testing, and growth promotion studies to ensure product safety and quality.

5. What are cGMP guidelines in the pharmaceutical industry?

Current Good Manufacturing Practices (cGMP) are regulations that ensure pharmaceutical products are consistently produced and controlled according to quality standards, minimizing risks related to contamination, mix-ups, and errors.