India's DMPLOI - Jobs & Networking AppIntas Pharmaceuticals Ltd. has announced a Walk-In Interview Drive for experienced professionals in Manufacturing, Quality Control, Microbiology, Engineering, and OSD departments. The recruitment drive will be conducted at Vapi, Gujarat, for positions based at the company’s Matoda, Ahmedabad manufacturing facility. Candidates with relevant pharmaceutical experience are invited to attend the interview with all required documents.
About Intas Pharmaceuticals
Intas Pharmaceuticals is a leading multinational pharmaceutical company engaged in the development, manufacturing, and marketing of pharmaceutical formulations. The company operates in more than 85 countries and derives nearly 70% of its revenue from international regulated markets, including the US and Europe. Intas is known for its strong focus on quality, regulatory compliance, innovation, and employee development.
Walk-In Interview Details
Company: Intas Pharmaceuticals Ltd.
Interview Type: Walk-In Drive
Interview Date: 26th July 2026 (Sunday)
Time: 09:30 AM to 05:00 PM
Venue: Fortune Park Galaxy, NH No. 48, GIDC, Vapi – 396195, Gujarat
Job Location: Matoda, Ahmedabad, Gujarat
Vacancy Details
1. Engineering Department
Position:
Senior Executive
Executive
Senior Officer
Department:
Instrumentation
QMS
Process Equipment Maintenance
21 CFR
HVAC
Qualification:
BE / B.Tech
Experience:
3 to 10 Years
2. OSD Manufacturing, Packing & QMS
Position:
Senior Officer
Officer
Associate
Qualification:
B.Pharm
M.Pharm
B.Sc
Diploma
ITI
Experience:
1 to 6 Years
3. Injectable Manufacturing, Packing & QMS
Position:
Senior Officer
Officer
Senior Associate
Associate
Qualification:
B.Pharm
M.Pharm
M.Sc
B.Sc
Diploma
ITI
Experience:
1 to 6 Years
4. Quality Control
Position:
Executive
Senior Officer
Officer
Qualification:
M.Sc (Organic Chemistry / Analytical Chemistry)
B.Pharm
M.Pharm
Experience:
3 to 7 Years
5. Microbiology
Position:
Executive
Senior Officer
Officer
Qualification:
M.Sc (Microbiology)
Experience:
3 to 7 Years
Candidate Requirements
Candidates should possess:
Good knowledge of cGMP guidelines
Understanding of Laboratory Safety Practices
Experience in Regulatory Approved Manufacturing Facilities
Relevant pharmaceutical manufacturing experience
Documents Required
Candidates should carry:
Updated Resume/CV
Educational Certificates
Experience Certificates
Latest Salary Slips
Current CTC Details
Identity Proof
Passport-size Photographs
Important Instructions
Candidates interviewed at Intas within the last six months are not eligible to apply.
Intas Pharmaceuticals does not charge any application fee at any stage of recruitment.
Beware of fraudulent job offers requesting money.
Why Join Intas Pharmaceuticals?
Global pharmaceutical company with operations in 85+ countries
Exposure to regulated markets including USFDA and EU
Excellent career growth opportunities
Modern manufacturing facilities
Learning-focused work environment
Competitive salary and employee benefits
Selection Process
Walk-In Registration
HR Screening
Technical Interview
Final HR Discussion
Offer Release (Subject to Selection)
How to Apply
Eligible candidates should directly attend the walk-in interview on 26th July 2026 at the mentioned venue with all required documents. Ensure your resume is updated and carry both original and photocopies of important certificates.
Technical FAQs
1. What is cGMP, and why is it important in pharmaceutical manufacturing?
Answer: cGMP (Current Good Manufacturing Practices) ensures pharmaceutical products are consistently manufactured and controlled according to quality standards, ensuring patient safety and regulatory compliance.
2. What instruments are commonly used in Quality Control laboratories?
Answer: QC laboratories typically use HPLC, GC, UV-Visible Spectrophotometer, Dissolution Tester, FTIR, Karl Fischer Titrator, and Analytical Balances for testing pharmaceutical products.
3. What are critical environmental monitoring activities in injectable manufacturing?
Answer: Environmental monitoring includes viable and non-viable particle monitoring, air sampling, surface monitoring, personnel monitoring, and differential pressure checks to maintain aseptic conditions.
4. What is HVAC validation in pharmaceutical manufacturing?
Answer: HVAC validation verifies that heating, ventilation, and air-conditioning systems consistently maintain the required temperature, humidity, pressure differentials, and cleanliness levels in controlled manufacturing areas.
5. What is the purpose of QMS in the pharmaceutical industry?
Answer: A Quality Management System (QMS) ensures effective management of deviations, change controls, CAPA, document control, audits, risk assessments, and regulatory compliance to maintain product quality.
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