India's DMPLOI - Jobs & Networking AppIntas Pharmaceuticals Limited has announced a major Walk-In Drive for SEZ operations at its Pharmez facility in Ahmedabad, Gujarat. The recruitment drive offers career opportunities for experienced candidates across OSD Manufacturing, OSD Packing, Injectable Manufacturing, Injectable Packing, Engineering, Quality Control (QC), Quality Assurance (QA), QMS, IPQA, Qualification, Stability, and related pharmaceutical departments.
Candidates with qualifications including ITI, Diploma, B.Pharm, M.Pharm, M.Sc, B.E., B.Tech, M.E., and M.Tech and relevant pharmaceutical industry experience can attend the walk-in interview scheduled from 16th to 18th July 2026.
Intas Pharmaceuticals Walk-In Drive Overview
Particulars Details
Company Name
Intas Pharmaceuticals Limited
Recruitment Type
Walk-In Drive
Business Unit
SEZ
Job Location
Ahmedabad, Gujarat
Interview Dates
16th to 18th July 2026
Interview Time
10:00 AM to 4:00 PM
Experience Required
3 to 13 Years, depending on the position
Qualifications
ITI, Diploma, B.Pharm, M.Pharm, M.Sc, B.E., B.Tech, M.E., M.Tech
Official Website
www.intaspharma.com
About Intas Pharmaceuticals Limited
Intas Pharmaceuticals is a leading multinational pharmaceutical formulation development, manufacturing, and marketing company with operations in more than 85 countries worldwide.
According to the official recruitment advertisement, Intas is growing at approximately 20% CAGR, and around 70% of its revenues come from international markets, particularly highly regulated markets such as the European Union and the United States.
The company is inviting experienced pharmaceutical professionals to participate in its upcoming walk-in recruitment drive for various technical and operational departments.
Intas Pharmaceuticals Vacancy Details
1. Technician – OSD Packing
Department: OSD – Packing (HV1 & CAM nMX)
Position: Technician
Qualification: Diploma / ITI
Experience: 3 to 12 Years
Candidates with relevant experience in Oral Solid Dosage (OSD) packing operations can attend the interview.
2. Senior Officer / Officer / Technician – OSD Manufacturing
Department: OSD – Manufacturing
Positions: Senior Officer / Officer / Technician
Qualification: B.Pharm / Diploma / ITI
Experience: 3 to 12 Years
Applicants should have relevant experience in pharmaceutical manufacturing operations, production equipment, GMP practices, and documentation.
3. Technician – Injectable Manufacturing
Department: Injectable – Manufacturing (Aseptic / Isolator / Ampoule)
Position: Technician
Qualification: Diploma / ITI
Experience: 3 to 12 Years
Candidates should possess practical experience in injectable manufacturing operations involving aseptic processing, isolator technology, or ampoule manufacturing.
4. Executive / Senior Executive / Assistant Manager – Engineering
Department: Engineering (Plant Maintenance & QMS – Injectables)
Positions: Executive / Senior Executive / Assistant Manager
Qualification: B.E. / B.Tech / M.E. / M.Tech
Experience: 7 to 13 Years
Applicants should have relevant pharmaceutical plant engineering experience, including equipment maintenance, utility systems, preventive maintenance, engineering documentation, and Quality Management System activities.
5. Technician – Injectable Packing
Department: Injectable – Packing
Position: Technician
Qualification: Diploma / ITI
Experience: 3 to 8 Years
Candidates should have experience handling pharmaceutical injectable packaging lines, equipment operations, documentation, and GMP compliance.
6. Senior Officer / Executive – Quality Control
Department: QC (HPLC / FP / Stability / AMV)
Positions: Senior Officer / Executive
Qualification: M.Sc / B.Pharm
Experience: 3 to 8 Years
Candidates with relevant Quality Control experience in HPLC analysis, finished product testing, stability studies, or analytical method validation (AMV) can apply.
7. Senior Officer / Executive – QC Microbiology
Department: QC (Micro – EM)
Positions: Senior Officer / Executive
Qualification: M.Sc / B.Pharm
Experience: 3 to 8 Years
Applicants should possess relevant pharmaceutical microbiology experience, particularly in Environmental Monitoring (EM) and associated GMP documentation.
8. Senior Officer / Executive / Senior Executive – Quality Assurance
Department: QA (Qualification / QMS / Doc Cell-Stability / IPQA – OSD/INJ)
Positions: Senior Officer / Executive / Senior Executive
Qualification: B.Pharm / M.Pharm
Experience: 3 to 10 Years
Candidates should have relevant Quality Assurance experience in areas such as qualification, Quality Management Systems, documentation cell, stability, and In-Process Quality Assurance (IPQA) for OSD or injectable facilities.
Walk-In Interview Schedule
Walk-In Dates: 16th to 18th July 2026
Interview Time: 10:00 AM to 4:00 PM
Candidates meeting the required qualification and experience criteria can directly attend the walk-in recruitment drive during the specified dates and timings.
Interview Venue
Intas Pharmaceuticals Ltd. (Pharmez)
Plot No. 5 to 14, Pharmez, Near Village Matoda,
Sarkhej-Bavla National Highway No. 8-A,
Taluka: Sanand, District: Ahmedabad – 382213, Gujarat.
Documents to Carry for the Interview
Candidates attending the Intas Pharmaceuticals walk-in interview should carry an updated resume/CV, recent passport-size photographs, educational certificates and mark sheets, experience certificates, current company appointment letter or employment proof, latest salary slips, Aadhaar Card or another valid government-issued photo ID, and any other relevant professional certificates.
Applicants should carry both original documents and photocopies wherever required for verification.
How to Apply for Intas Pharmaceuticals Recruitment
This recruitment is being conducted through a direct walk-in interview process. Interested candidates should carefully verify their eligibility for the relevant position, update their resume with accurate employment and technical experience details, prepare the required documents, and attend the interview at the specified venue between 16th and 18th July 2026.
Candidates should preferably arrive early to complete registration and document verification procedures.
Important Instructions for Candidates
Candidates should apply only for positions matching their educational qualifications and professional experience. Experience requirements vary from 3 to 13 years, depending on the department and designation.
Applicants working in pharmaceutical manufacturing environments should be prepared to answer technical questions related to their department, including GMP, SOPs, equipment operations, data integrity, deviation management, CAPA, validation, qualification, safety procedures, and regulatory compliance.
Recruitment policies, candidate selection, salary packages, and final appointment decisions remain at the discretion of Intas Pharmaceuticals Limited.
Why Join Intas Pharmaceuticals?
Intas Pharmaceuticals provides professionals with opportunities to work in a global pharmaceutical organization serving regulated international markets. Employees can gain exposure to modern manufacturing technologies, Quality Management Systems, regulatory requirements, sophisticated analytical instruments, aseptic processing technologies, engineering systems, and large-scale pharmaceutical operations.
The recruitment drive can be particularly relevant for experienced pharmaceutical professionals seeking career growth opportunities in manufacturing, packing, quality, and engineering functions.
5 Technical FAQs for Intas Pharmaceuticals Walk-In Interview
1. What is the difference between a deviation, CAPA, and change control in the pharmaceutical industry?
A deviation is an unplanned departure from an approved procedure, process, specification, or established standard. CAPA (Corrective and Preventive Action) involves identifying the root cause of an existing problem, correcting it, and implementing measures to prevent recurrence. Change control is a formal system used to evaluate, approve, implement, and document planned changes to facilities, equipment, processes, materials, analytical methods, or documents.
2. What is Environmental Monitoring (EM) in injectable pharmaceutical manufacturing?
Environmental Monitoring is a systematic program used to assess the microbiological and particulate conditions of controlled pharmaceutical manufacturing areas. It may include active air sampling, passive air monitoring through settle plates, surface monitoring using contact plates or swabs, personnel monitoring, and non-viable particle monitoring. EM is particularly important for maintaining contamination control in aseptic manufacturing areas.
3. What is the purpose of HPLC in pharmaceutical Quality Control?
High-Performance Liquid Chromatography (HPLC) is widely used for the identification, separation, and quantitative analysis of pharmaceutical compounds. It is commonly applied for assay determination, impurity analysis, dissolution testing, content uniformity, stability studies, and related substance testing. Proper system suitability, calibration, method validation, and data integrity practices are essential during HPLC analysis.
4. What are the major GMP requirements during OSD and injectable manufacturing?
Major GMP requirements include following approved SOPs and Batch Manufacturing Records, maintaining personnel hygiene, preventing contamination and cross-contamination, ensuring equipment cleanliness and line clearance, maintaining accurate documentation, complying with data integrity principles, controlling environmental conditions, investigating deviations, and performing manufacturing operations according to validated processes.
Injectable manufacturing additionally requires strict contamination control, aseptic practices, environmental monitoring, sterilization controls, and compliance with cleanroom procedures.
5. What is equipment qualification, and what are DQ, IQ, OQ, and PQ?
Equipment qualification provides documented evidence that pharmaceutical equipment and systems are suitable for their intended use.
DQ (Design Qualification) verifies that the proposed equipment design meets user and GMP requirements.
IQ (Installation Qualification) confirms that equipment has been installed correctly according to approved specifications.
OQ (Operational Qualification) demonstrates that the equipment operates correctly throughout predetermined operating ranges.
PQ (Performance Qualification) verifies that the equipment consistently performs effectively under routine production conditions.
Conclusion
The Intas Pharmaceuticals Walk-In Drive 2026 offers employment opportunities for experienced professionals across OSD Manufacturing, OSD Packing, Injectable Manufacturing, Injectable Packing, Engineering, Quality Control, Microbiology, Quality Assurance, QMS, IPQA, Qualification, and Stability departments.
Eligible candidates with 3 to 13 years of relevant experience can attend the walk-in interviews from 16th to 18th July 2026, between 10:00 AM and 4:00 PM, at the Intas Pharmaceuticals Pharmez facility in Ahmedabad, Gujarat.
Candidates are advised to verify their eligibility, prepare their technical interview topics, carry all necessary documents, and check the official company website for additional information before attending the recruitment drive.
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