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Intas Pharmaceuticals Ltd., a leading global pharmaceutical company with a presence in over 85 countries, is hiring for various roles at our Pharmez facility in Ahmedabad, Gujarat. With a 20% CAGR and 70% of revenues from regulated markets like the EU and US, Intas is committed to creating a world of good health, happiness, and hope.
Certified as a Great Place to Work, we offer a dynamic, regulatory-compliant environment for professionals passionate about pharmaceutical excellence. Join us for our walk-in drive in Baroda to explore exciting career opportunities!
Walk-In Interview Details
- Date: Sunday, July 6, 2025
- Time: 9:30 AM to 3:00 PM
- Venue: Grand Mercure Surya Palace, Sayajigunj, Vadodara, Gujarat – 390020
- Job Location: Intas Pharmez, Plot No. 5 to 14, Pharmez, Near Village Matoda, Sarkhej-Bavla Highway, Ahmedabad, Gujarat – 382213
Required Documents:
- Updated resume (2 copies)
- Original and photocopies of final year mark sheets/degree certificate
- CTC breakup and last 3 months’ salary slips
- Aadhar card and PAN card
- Passport-size photographs (2)
Note:
- Candidates must have experience in regulated plants (e.g., USFDA, MHRA, EU-GMP).
- Candidates interviewed at Intas in the last 6 months are ineligible.
- All positions require openness to shift duties.
Job Opportunities
Engineering (Instrumentation / Process Equipment Maintenance / HVAC)
- Designation: Assistant Manager / Senior Executive / Executive / Senior Officer / Technician
- Qualification: B.E / B.Tech / Diploma / ITI (Instrumentation, Mechanical, or Electrical)
- Experience: 3–12 years
- Vacancies: Multiple (exact number TBD)
Responsibilities:
- Perform maintenance of process equipment (e.g., reactors, tablet compression machines) and HVAC systems.
- Conduct instrumentation calibration and troubleshooting.
- Ensure compliance with cGMP and regulatory standards (USFDA, MHRA).
- Maintain documentation for preventive maintenance and audits.
Injectable – Manufacturing & Packing
- Designation: Senior Officer / Officer / Associate
- Qualification: B.Pharm / M.Pharm / M.Sc / B.Sc / Diploma
- Experience: 1–7 years
- Vacancies: Multiple (exact number TBD)
Responsibilities:
- Operate and monitor injectable manufacturing processes (e.g., vial/ampoule filling, sealing).
- Perform packing operations for sterile products, ensuring cGMP compliance.
- Maintain Batch Manufacturing Records (BMR) and Batch Packing Records (BPR).
- Support regulatory audits and process validations.
Quality Assurance – IPQA (OSD & Sterile)
- Designation: Senior Officer / Officer / Associate
- Qualification: B.Pharm / M.Sc
- Experience: 1–7 years
- Vacancies: Multiple (exact number TBD)
Responsibilities:
- Conduct in-process quality checks for Oral Solid Dosage (OSD) and sterile products.
- Perform line clearance, sampling, and BMR/BPR reviews.
- Manage deviations, CAPA, and audit compliance (USFDA, MHRA).
- Ensure adherence to cGMP and Good Documentation Practices (GDP).
Quality Control (Chemical & Microbiology)
- Designation: Officer / Senior Officer / Executive
- Qualification: B.Sc / M.Sc (Organic Chemistry, Analytical Chemistry) / B.Pharm / M.Pharm
- Experience: 2–10 years
- Vacancies: Multiple (exact number TBD)
Responsibilities:
- Perform chemical analysis using HPLC, GC, UV, and dissolution apparatus.
- Conduct microbiological testing, including sterility and environmental monitoring.
- Ensure GLP compliance and maintain accurate laboratory records.
- Support stability studies and regulatory inspections.
OSD – Manufacturing & Packing (Blister Packing & Secondary Packing)
- Designation: Senior Officer / Officer / Associate / Technician
- Qualification: B.Pharm / ITI / Diploma / M.Sc
- Experience: 1–7 years
- Vacancies: Multiple (exact number TBD)
Responsibilities:
- Operate OSD manufacturing equipment (e.g., compression, granulation, coating machines).
- Perform blister packing and secondary packing operations.
- Ensure cGMP compliance and maintain accurate BMR/BPR documentation.
- Support process validation and regulatory audits.
Why Join Intas Pharmaceuticals?
- Global Leader: Contribute to a top multinational pharmaceutical company with a presence in 85+ countries and a 20% CAGR.
- Regulatory Excellence: Work in USFDA, MHRA, and EU-GMP compliant facilities, ensuring high-quality standards.
- Great Place to Work: Join a certified workplace with a 3.8/5 rating on AmbitionBox, offering a supportive culture and career growth opportunities.
- Innovative Environment: Be part of a company with 300+ scientists and 10,000+ employees driving innovation in formulations and APIs.
How to Apply
- Walk-In: Attend the interview on July 6, 2025, at the Grand Mercure Surya Palace, Vadodara, with all required documents.
- For Those Unable to Attend: Email your updated CV to hrd@intaspharma.com, mentioning the specific role and department (e.g., “QC Officer – Chemical”) in the subject line. Include total experience, current CTC, expected CTC, and notice period.
- Contact: For queries, reach out to the HR department via www.intaspharma.com or email hrd@intaspharma.com.
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Note: Candidates must have formulation pharma experience in regulated plants (USFDA, MHRA, EU-GMP).
About Intas Pharmaceuticals
Founded in 1977, Intas Pharmaceuticals Ltd. is headquartered in Ahmedabad, Gujarat, and is a leading global player in pharmaceutical formulation development, manufacturing, and marketing. With 18 manufacturing facilities, 11 in India, and a strong focus on generics and biosimilars, Intas serves highly regulated markets like the EU and US.
Our Pharmez facility in Ahmedabad is a state-of-the-art hub for OSD and injectable production, supported by over 300 ANDAs filed with the USFDA. Learn more at www.intaspharma.com.
Important Disclaimer
Intas Pharmaceuticals Ltd. does not charge any fees for job applications, processing, training, or testing. Report suspicious requests to hrd@intaspharma.com.
Join Intas Pharmaceuticals and be part of a global leader creating a world of good health and happiness!