Intas Pharmaceuticals Ltd., a global leader in pharmaceutical formulation development, manufacturing, and marketing, is hosting a walk-in interview drive for multiple roles at our Matoda facility in Ahmedabad. With a presence in over 85 countries, a 20% CAGR, and 70% of revenues from highly 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, Intas offers a dynamic environment for professionals to grow and contribute to innovative healthcare solutions.
Why Work at Intas Pharmaceuticals?
Intas, headquartered in Ahmedabad, is a vertically integrated pharmaceutical giant with 19,000+ employees and 21 manufacturing facilities worldwide. Rated 4.1/5 on AmbitionBox based on 3.5k+ reviews, Intas is praised for job security (4.0/5) and work-life balance (3.9/5). Our Matoda facility is USFDA, MHRA, and EU-GMP approved, providing exposure to cutting-edge technology and cGMP-compliant processes.
- Work in a globally recognized organization with a $2.5 billion+ revenue milestone
- Contribute to a diverse portfolio, including injectables, oral solid dosages (OSD), and biologics
- Benefit from a supportive culture with transport facilities and polite, accessible management
- Opportunities for skill development in a regulatory-compliant environment
Walk-In Interview Details
- Date: April 26, 2025 (Saturday)
- Time: 9:30 AM – 2:00 PM
- Venue: Intas Pharmaceuticals Ltd., Matoda, Plot No. 457, 458, Sarkhej-Bavla Highway, Matoda Village, Sanand Taluka, Ahmedabad, Gujarat 382210
- Job Location: Matoda, Ahmedabad
Requirements:
- Updated resume
- Educational certificates (mark sheets, degree certificates)
- Experience documents (offer letters, relieving letters)
- Salary documents (latest salary slip, CTC breakup)
- Passport-size photo, Aadhar, and PAN card copies
Important Notes:
- Candidates who attended an Intas interview in the last six months are not eligible
- Thorough knowledge of cGMP norms and laboratory safety is mandatory
- Experience in USFDA, MHRA, or EU-GMP regulated facilities is preferred
- Intas does not charge any fees for job applications, processing, training, or testing. Beware of fraudulent activities.
Contact: Email resumes to hr_matoda@intaspharma.com, mentioning the desired position and department in the subject line (e.g., “Officer QA-IPQA Injectable Application”).
Open Positions
We are hiring for Quality Assurance (QA), Quality Control (QC), and Manufacturing (OSD and Injectable) roles at our Matoda facility. Candidates must have relevant experience in pharmaceutical manufacturing and a strong understanding of cGMP standards.
1. Quality Assurance – IPQA (Injectable/OSD) & QMS/Documentation/Validation and Qualification
- Position: Officer / Senior Officer / Executive / Senior Executive
- Qualification: B.Pharm / M.Pharm / M.Sc.
- Experience: 2–9 years
Skills Required:
- Expertise in In-Process Quality Assurance (IPQA) for Injectable (autoclave, sterilizers, filling) or OSD (granulation, coating, tablets, capsules)
- Proficiency in QMS (deviations, CAPA, change control), documentation, and validation/qualification
- Knowledge of equipment audit trails, BMR/BPR review, and line clearance
- Experience in USFDA, MHRA, or EU-GMP regulated facilities
Responsibilities:
- Conduct IPQA checks during manufacturing and packing
- Manage QMS activities and validation protocols
- Ensure compliance with cGMP and regulatory standards
- Review batch records and support audit preparedness
2. Quality Control
- Position: Officer / Senior Officer / Executive
- Qualification: B.Sc. / M.Sc. (Organic Chemistry, Analytical Chemistry) / B.Pharm / M.Pharm
- Experience: 2–7 years
Skills Required:
- Proficiency in analytical testing for Finished Goods (FG), Stability, and Analytical Method Validation (AMV)
- Hands-on experience with instruments like HPLC, GC, UV-Vis, and Dissolution testers
- Familiarity with Chromeleon or Empower software
- Knowledge of cGMP, GLP, and regulatory compliance
Responsibilities:
- Perform analytical testing and stability studies
- Document results and ensure compliance with pharmacopeial standards
- Support method validation and instrument calibration
- Maintain laboratory safety and data integrity
3. OSD – Manufacturing/Dispensing/QMS
- Position: Senior Officer / Officer / Associate
- Qualification: B.Sc. / M.Sc. / B.Pharm / M.Pharm / Diploma
- Experience: 1–5 years
Skills Required:
- Experience in OSD manufacturing (granulation, compression, coating, capsule filling)
- Knowledge of dispensing processes and QMS activities
- Familiarity with equipment like GEA, Glatt, KORSCH, or CADMACH
- Understanding of cGMP and SOP compliance
Responsibilities:
- Operate and monitor OSD manufacturing and dispensing equipment
- Perform line clearance and batch documentation
- Support QMS tasks (deviations, CAPA)
- Ensure adherence to safety and regulatory standards
4. Injectable – Manufacturing (Aseptic Operations/QMS/SKID/Multi-Vessel/SVP)
- Position: Senior Officer / Officer / Associate
- Qualification: B.Sc. / M.Sc. / B.Pharm / M.Pharm / Diploma
- Experience: 1–5 years
Skills Required:
- Expertise in aseptic operations, SKID, multi-vessel systems, or Small Volume Parenterals (SVP)
- Knowledge of QMS processes and cGMP compliance
- Experience with equipment like autoclaves, vial filling machines, or lyophilizers
- Familiarity with USFDA or MHRA audit requirements
Responsibilities:
- Conduct aseptic manufacturing and filling operations
- Maintain cleanroom standards and equipment functionality
- Document processes and report deviations
- Support QMS and regulatory compliance activities
How to Apply
Attend the walk-in interview on April 26, 2025, from 9:30 AM to 2:00 PM at Intas Pharmaceuticals Ltd., Matoda, Ahmedabad. Alternatively, email your updated resume to hr_matoda@intaspharma.com, ensuring the subject line specifies the position and department. Bring all required documents listed above to the interview. For more details, visit www.intaspharma.com.
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Join Intas’ Mission!
Be part of a leading pharmaceutical organization that drives innovation and quality across 85+ countries. At Intas Pharmaceuticals, your expertise will contribute to life-saving formulations in a USFDA-approved facility. We look forward to meeting you at our Matoda walk-in drive on April 26, 2025!
