India's DMPLOI - Jobs & Networking AppIntas Pharmaceuticals Ltd. has announced a Walk-In Interview Drive for experienced professionals in Engineering, Quality Assurance, Quality Control, Microbiology, Injectable Manufacturing, and OSD Manufacturing. This is an excellent opportunity for candidates with experience in the pharmaceutical industry to join one of India’s leading multinational pharmaceutical companies.
The walk-in interview will be held on 12 July 2026 (Sunday) at Papaya Tree, Indore, for positions based at Matoda, Ahmedabad.
About Intas Pharmaceuticals
Intas Pharmaceuticals is a globally recognized pharmaceutical company engaged in formulation development, manufacturing, and marketing. The company operates in more than 85 countries and generates around 70% of its revenue from international markets, including highly regulated markets such as the US and Europe. Intas is known for maintaining high-quality manufacturing standards and offering excellent career growth opportunities.
Walk-In Interview Details
Company: Intas Pharmaceuticals Ltd.
Interview Type: Walk-In Drive
Walk-In Date: 12 July 2026 (Sunday)
Time: 09:30 AM to 05:00 PM
Venue: Papaya Tree, A.B. Road, Rau, Indore, Madhya Pradesh
Job Location: Matoda, Ahmedabad
Departments & Vacancies
1. Engineering
Positions
Senior Executive
Executive
Senior Officer
Departments
Instrumentation
QMS
Process Equipment Maintenance
21 CFR
HVAC
Qualification
BE / B.Tech
Experience
2–9 Years
2. Quality Assurance (QA)
Positions
Officer
Senior Officer
Executive
Departments
QMS
Documentation
Validation & Qualification
IPQA (Parenteral / OSD)
Qualification
B.Pharm
M.Pharm
M.Sc.
Experience
2–7 Years
3. Quality Control (QC)
Positions
Officer
Senior Officer
Executive
Qualification
B.Sc.
M.Sc. (Organic Chemistry / Analytical Chemistry)
B.Pharm
M.Pharm
Experience
3–7 Years
4. Microbiology
Positions
Officer
Senior Officer
Executive
Qualification
M.Sc. (Microbiology)
Experience
3–7 Years
5. Injectable Manufacturing & Packing / QMS
Positions
Associate
Officer
Senior Officer
Qualification
B.Pharm
M.Pharm
M.Sc.
B.Sc.
Diploma
ITI
Experience
1–6 Years
6. OSD Manufacturing & Packing
Positions
Associate
Officer
Senior Officer
Qualification
B.Pharm
M.Pharm
Diploma
ITI
Experience
1–6 Years
Documents to Carry
Candidates should bring:
Updated Resume
Educational Certificates
Experience Certificates
Latest Salary Documents
Government Photo ID
Passport-size Photographs
Important Instructions
Candidates who have attended an Intas interview in the last six months are requested not to apply.
Candidates should have sound knowledge of cGMP and Laboratory Safety.
Relevant experience in a regulatory-approved pharmaceutical facility is preferred.
Intas Pharmaceuticals does not charge any fee for recruitment. Avoid fraudulent job offers requesting payment.
Why Join Intas Pharmaceuticals?
Global pharmaceutical company with operations in 85+ countries
Excellent learning and career growth opportunities
Exposure to regulated markets like USFDA and EU
Modern manufacturing facilities
Competitive salary and employee benefits
Technical FAQs
1. What is cGMP, and why is it important in pharmaceutical manufacturing?
Answer: cGMP (Current Good Manufacturing Practices) ensures medicines are consistently manufactured and controlled according to quality standards. It helps maintain product safety, efficacy, and regulatory compliance.
2. What is IPQA in pharmaceutical manufacturing?
Answer: In-Process Quality Assurance (IPQA) monitors manufacturing activities during production to ensure processes comply with SOPs, GMP guidelines, and product quality requirements.
3. What is the purpose of equipment qualification?
Answer: Equipment qualification verifies that equipment is correctly installed (IQ), operates properly (OQ), and consistently performs as intended (PQ), ensuring reliable manufacturing processes.
4. What microbiological tests are commonly performed in pharmaceutical industries?
Answer: Common tests include microbial limit testing, environmental monitoring, sterility testing, water testing, endotoxin testing, and media preparation to maintain aseptic manufacturing standards.
5. What are the key responsibilities of a Quality Control analyst?
Answer: QC analysts perform raw material testing, in-process testing, finished product analysis, stability studies, instrument calibration, documentation, and ensure compliance with pharmacopoeial and regulatory standards.
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