Join Intas Pharmaceuticals Ltd., a leading global pharmaceutical company founded in 1977, headquartered in Ahmedabad, Gujarat. With a turnover of ₹8,500 Cr, operations in 85+ countries, and a 20% CAGR, Intas is renowned for its USFDA, EU-GMP, WHO-GMP, and ISO 9001:2015-certified facilities, producing injectables, oral solid dosages (OSD), and biologics. Certified as a Great Place to Work, Intas derives 70% of its revenue from regulated markets like the EU and US.
We’re hosting a walk-in drive on May 17, 2025, at our Matoda facility in Ahmedabad for Quality Assurance (QA) and Manufacturing roles, targeting professionals with 1-9 years of experience in pharmaceutical manufacturing.
Event Details: Walk-In Drive
This walk-in drive seeks candidates for QA (IPQA, QMS, Documentation, Validation) and Manufacturing (OSD, Injectable) roles at our Matoda facility, a key hub for injectables and OSD production. Candidates with regulatory exposure (USFDA, EU-GMP) are preferred.
Date and Time
- Date: Saturday, May 17, 2025
- Time: 9:30 AM – 2:00 PM IST
Venue
Intas Pharmaceuticals Ltd.
Plot No. 457, 458, Sarkhej Bavla Highway, Matoda Village, Sanand Taluka, Ahmedabad, Gujarat – 382210
Job Location
- Same as venue: Intas Pharmaceuticals Ltd., Matoda, Ahmedabad, Gujarat – 382210
Job Opportunities at Intas Pharmaceuticals
We’re hiring for Officer, Senior Officer, Executive, Senior Executive, and Associate roles in QA and Manufacturing to support our Matoda facility, compliant with cGMP standards. All positions require experience in regulatory-approved facilities.
1. Quality Assurance – IPQA (Injectable), IPQA (OSD), QMS, Documentation, Validation and Qualification
- Position: Officer / Senior Officer / Executive / Senior Executive
- Qualification: B.Pharm, M.Pharm, M.Sc. (Chemistry, Microbiology)
- Experience: 2-9 years in QA for injectable or OSD facilities
- Key Responsibilities:
- IPQA (Injectable/OSD): Conduct in-process checks, line clearances, and sampling during manufacturing
- QMS: Manage deviations, CAPA, change controls, and OOS/OOT investigations
- Documentation: Review BMRs, BPRs, SOPs, and ensure 21CFR Part 11 compliance
- Validation/Qualification: Perform equipment qualification, process validation, and cleaning validation
- Support USFDA/EU-GMP audits and ensure laboratory safety
- Key Skills:
- Expertise in IPQA, QMS, and validation protocols
- Knowledge of cGMP, ICH Q9/Q10, and regulatory standards
- Proficiency in documentation and audit preparation
- Strong analytical skills for deviation handling
- Openings: Multiple (likely 6-10 based on QA operations)
- Salary: ₹4.0–12.0 Lakhs/year (estimated based on experience)
2. OSD Manufacturing – Manufacturing, Dispensing, QMS
- Position: Senior Officer / Officer / Associate
- Qualification: B.Sc. (Chemistry), M.Sc., B.Pharm, M.Pharm, Diploma (Pharmacy)
- Experience: 1-5 years in OSD manufacturing
- Key Responsibilities:
- Manufacturing: Operate equipment for granulation, compression, coating, and packing
- Dispensing: Weigh and dispense raw materials per BMR
- QMS: Support deviation reporting and CAPA implementation
- Ensure cGMP compliance and accurate documentation
- Monitor in-process parameters and support process validation
- Key Skills:
- Proficiency in OSD equipment (e.g., RMG, Fette, CAM)
- Knowledge of cGMP and QMS processes
- Precision in dispensing and documentation
- Ability to troubleshoot manufacturing issues
- Openings: Multiple (likely 8-12 based on OSD lines)
- Salary: ₹2.5–6.0 Lakhs/year (estimated based on experience)
3. Injectable Manufacturing – Aseptic Operations, QMS, SKID, Multi-Vessel, SVP, Visual Inspector
- Position: Senior Officer / Officer / Associate
- Qualification: B.Pharm, M.Pharm, M.Sc., B.Sc., Diploma (Pharmacy), ITI
- Experience: 1-5 years in injectable manufacturing
- Key Responsibilities:
- Aseptic Operations: Perform filling, sealing, and compounding in cleanrooms
- SKID/Multi-Vessel: Operate SKID systems and multi-vessel setups for SVP
- Visual Inspector: Inspect vials/ampoules for defects (particulates, cracks)
- QMS: Document deviations and support CAPA
- Ensure cGMP compliance and maintain aseptic behaviors
- Key Skills:
- Expertise in aseptic techniques and injectable equipment
- Knowledge of cGMP and QMS for injectables
- Precision in visual inspection and documentation
- Familiarity with SKID and multi-vessel operations
- Openings: Multiple (likely 10-15 based on injectable lines)
- Salary: ₹2.5–6.0 Lakhs/year (estimated based on experience)
Why Join Intas Pharmaceuticals?
Intas, with 18,000+ employees, is rated 4.0/5 on AmbitionBox for job security (4.2/5) and work culture (3.9/5). Our Matoda facility, one of 14 global manufacturing sites, supports injectables and OSD for 85+ countries, with USFDA and EU-GMP approvals. Employees praise regulatory exposure (4.1/5) and Great Place to Work certification but note high-pressure roles (3.7/5 work-life balance). With 70% international revenue and a focus on biologics, Intas offers a dynamic career platform.
Key Benefits
- Work in a USFDA/EU-GMP-compliant facility
- Gain expertise in aseptic operations, QMS, and validation
- Support global markets with innovative medicines
- Join a Great Place to Work with ₹8,500 Cr turnover
- Access growth in Ahmedabad’s pharma hub
How to Apply
Attend the walk-in drive on May 17, 2025, from 9:30 AM to 2:00 PM at Intas Pharmaceuticals, Matoda, Ahmedabad. Bring:
- Updated resume
- All educational certificates (B.Pharm, M.Pharm, M.Sc., B.Sc., Diploma, ITI)
- Experience letters and salary documents (last 3 months’ payslips, increment letter)
- Aadhar and PAN cards
- Passport-size photographs (2)
Verified by Trusted HRs
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Preparation:
- QA: Review IPQA, QMS, validation, and USFDA/EU-GMP audits
- OSD Manufacturing: Study granulation, compression, and cGMP
- Injectable Manufacturing: Prepare for aseptic operations, visual inspection, and SKID
- Be ready to discuss regulatory exposure and laboratory safety
Note: Candidates interviewed at Intas in the last 6 months should not apply. Intas does not charge recruitment fees; verify communications via @intaspharma.com emails. For queries, contact hr@intaspharma.com.
About Intas Pharmaceuticals
Intas operates 14 manufacturing facilities, with Matoda specializing in injectables and OSD. Producing 10,000+ SKUs, we lead in oncology, neurology, and respiratory therapies, with approvals from USFDA, EMA, and MHRA. Our R&D center, with 500+ scientists, drives innovation, supported by a 7% revenue investment.
Our Mission
- Create a world of good health, happiness, and hope
- Deliver innovative, affordable medicines
- Foster a collaborative, inclusive workplace
Attend the walk-in drive on May 17, 2025, at Intas, Matoda, and join our mission to advance global healthcare!