Intas Pharmaceuticals Ltd., a global leader in pharmaceutical formulation development, manufacturing, and marketing, is hosting a walk-in interview drive in Aurangabad for multiple roles at our Ahmedabad facilities. 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 a Great Place to Work certified organization. Rated 4.1/5 on AmbitionBox for job security, we invite skilled professionals to join our mission of creating a world of good health, happiness, and hope.
Why Work at Intas Pharmaceuticals?
Intas, headquartered in Ahmedabad, employs 19,000+ professionals across 21 manufacturing facilities, with 10+ USFDA and MHRA-approved sites. Our Ahmedabad facilities specialize in sterile injectables, oral solid dosages (OSD), and biologics, offering exposure to cutting-edge technology and cGMP-compliant processes. With a 3.9/5 rating for work-life balance, Intas provides a supportive environment for career growth.
- Work in USFDA, MHRA, and EU-GMP approved facilities exporting to 85+ countries
- Contribute to a portfolio of 2000+ products across oncology, cardiology, and neurology
- Benefit from a collaborative culture with transport facilities and accessible management
- Gain expertise in sterile manufacturing, quality systems, and regulatory compliance
Walk-In Interview Details
- Date: April 27, 2025 (Sunday)
- Time: 9:00 AM – 3:30 PM
- Venue: Lemon Tree Hotel, R 7/2, Airport Road, CIDCO Cannought, Chilkalthana, Chhatrapati Sambhaji Nagar, Maharashtra 431210
- Job Location: Ahmedabad, Gujarat
Requirements:
- Updated resume
- Original and photocopies of final year mark sheets and degree certificates
- Experience documents (offer letters, relieving letters)
- Salary documents (CTC breakup, latest salary slip)
- Passport-size photo, Aadhar, and PAN card copies
Important Notes:
- Candidates must have pharmaceutical experience in USFDA, MHRA, or EU-regulated plants
- Openness to work in shift duties is mandatory
- Candidates who attended an Intas interview in the last six months are not eligible
- Intas does not charge any fees for job applications, processing, training, or testing. Beware of fraudulent activities.
Contact: Email resumes to hr_ahmedabad@intaspharma.com, mentioning the position and department in the subject line (e.g., “Officer QC Application”).
Open Positions
We are hiring for Quality Control (QC), Quality Assurance (QA), Engineering, Instrumentation, and Sterile/Injectable Manufacturing/Packing roles at our Ahmedabad facilities. Candidates must have relevant experience in formulation pharmaceuticals, cGMP compliance, and familiarity with regulated environments.
1. Quality Control (QC – FG/Stability/AMV)
- Position: Officer to Executive
- Qualification: M.Sc. (Chemistry) / B.Pharm / M.Pharm
- Experience: 2–7 years
Skills:
- Expertise in analysis of Finished Goods (FG), Analytical Method Validation (AMV), and Stability testing
- Hands-on experience with HPLC, GC, and knowledge of Chromeleon software (preferred)
- Strong understanding of cGMP, GLP, and laboratory safety protocols
Responsibilities:
- Perform analytical testing for FG, stability, and method validation
- Document results and ensure compliance with pharmacopeial standards
- Support QMS activities (OOS, OOT, deviations) and instrument calibration
2. Quality Assurance (Lab QA)
- Position: Senior Officer to Senior Executive
- Qualification: M.Sc. / B.Pharm
- Experience: 3–10 years
Skills:
- Good exposure to Lab QA activities, including review of analytical data and lab compliance
- Knowledge of QMS (deviations, CAPA, change control) and audit preparation
- Familiarity with USFDA/MHRA regulatory requirements
Responsibilities:
- Oversee lab QA processes, ensuring data integrity and compliance
- Review analytical records, stability data, and validation reports
- Support internal and regulatory audits
3. Quality Assurance (IPQA/Qualification – Sterile Background Only)
- Position: Officer to Executive
- Qualification: B.Pharm / M.Pharm / M.Sc.
- Experience: 2–7 years
Skills:
- Expertise in Sterile IPQA (vial filling, PFS, lyophilization) and equipment qualification
- Knowledge of aseptic processes, line clearance, and BMR/BPR review
- Familiarity with cGMP and regulatory compliance (USFDA, MHRA)
Responsibilities:
- Conduct IPQA checks during sterile manufacturing and packing
- Manage equipment and process qualification activities
- Ensure compliance with sterile facility standards and QMS
4. Engineering (Plant Maintenance – Sterile)
- Position: Technician / Executive / Assistant Manager / Manager
- Qualification: M.Sc. / B.Pharm / M.Pharm (relevant experience in engineering roles)
- Experience: 2–15 years
Skills:
- Expertise in plant maintenance and instrumentation in sterile facilities
- Knowledge of HVAC, autoclaves, lyophilizers, and cleanroom systems
- Familiarity with preventive maintenance and cGMP compliance
Responsibilities:
- Perform maintenance of sterile manufacturing equipment
- Support instrumentation and calibration activities
- Ensure uptime and compliance with regulatory standards
5. Instrumentation (Sterile)
- Position: Technician / Executive / Assistant Manager
- Qualification: M.Sc. / B.Pharm / M.Pharm (relevant experience in instrumentation)
- Experience: 2–15 years
Skills:
- Proficiency in instrumentation maintenance in sterile facilities
- Experience with PLC, SCADA, and calibration of critical equipment
- Knowledge of cGMP and safety protocols
Responsibilities:
- Maintain and calibrate instrumentation systems in sterile areas
- Troubleshoot equipment issues and document activities
- Support regulatory audits and compliance
6. Sterile/Injectable – Manufacturing/Packing
- Position: Technician / Operator / Officer / Senior Officer
- Qualification: Diploma (Engineering) / D.Pharm / B.Pharm / M.Pharm
- Experience: 2–6 years
Skills:
- Expertise in Complex SKID, NODS, Aseptic operations (PFS, Vials, Liquid), Autoclave, Lyophilizer, and Batch Manufacturing
- Knowledge of sterile secondary packing, track-and-trace systems, and visual inspection
- Familiarity with cGMP and USFDA/MHRA audit requirements
Responsibilities:
- Operate and monitor sterile manufacturing and packing equipment
- Perform aseptic operations, visual inspections, and batch documentation
- Ensure compliance with SOPs, cGMP, and regulatory standards
How to Apply
Attend the walk-in interview on April 27, 2025, from 9:00 AM to 3:30 PM at Lemon Tree Hotel, Aurangabad. Bring all required documents (originals and photocopies) as listed above. Alternatively, email your updated resume to hr_ahmedabad@intaspharma.com, specifying the position and department in the subject line. For more details, visit www.intaspharma.com.
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Join Intas’ Mission!
Join a global pharmaceutical leader driving innovation and quality across 85+ countries. At Intas Pharmaceuticals, your expertise in QA, QC, engineering, or sterile manufacturing will contribute to life-saving therapies in our USFDA-approved Ahmedabad facilities. We look forward to meeting you at our Aurangabad walk-in drive on April 27, 2025!
