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TAPI, a Global Pharma Leader, Launches Major Recruitment Drive in India
Malanpur, Gajraula, & Greater Noida Facilities Seek Experienced Professionals Across Production, R&D, and Engineering
TAPI, a leading international supplier of Active Pharmaceutical Ingredients (APIs), has announced a significant recruitment drive for its Indian manufacturing facilities. The company is seeking experienced professionals across various departments, including Production, Quality Control, Research & Development, and Engineering, to support its growing operations in Malanpur (Madhya Pradesh), Gajraula, and Greater Noida (Uttar Pradesh).
A cornerstone of the pharmaceutical industry, TAPI boasts a reliable history spanning over 80 years in the generic API sector. The company is a critical partner to the global pharmaceutical community, supplying APIs to 80% of the world’s top 50 pharmaceutical companies. This recruitment initiative underscores its continued expansion and commitment to maintaining the highest standards of quality and innovation.
A Call for Experienced Pharma & Chemical Talent
The open positions are specifically targeted at professionals with a background in pharmaceutical API or chemical manufacturing. The company has emphasized that “Pharma API / Chemical experience is a Must” for all roles, seeking to onboard candidates who can immediately contribute to its complex and regulated manufacturing environment.
Detailed Breakdown of Job Openings
The recruitment drive covers a wide range of specializations and experience levels, from early-career professionals to senior managers.
1. Production
Experience: 1 to 10 years (multiple brackets)
Qualification: M.Sc. (Chemistry) / B.Tech. or Diploma (Chemical)
2. Quality Control (HPLC / GC / Wet Lab / Micro / QMS)
Experience: 2 to 14 years (multiple brackets)
Qualification: M.Sc. (Chemistry) or M.Sc. (Microbiology) for QC Micro roles.
3. Research & Development
· Pilot Researcher: 2-10 years experience with a B.Tech./B.E. (Chemical)
· Analytical R&D Analyst: 3-10 years experience with an M.Sc. (Chemistry)
4. Engineering & EHS
· Manager – EHS (Safety): 12-15 years in API/Chemical with an M.Sc. (Chemistry) / B.Tech. (Chemical)
· Manager – Maintenance/Engineering (Mechanical): Min. 10 years in API/Chemical with a B.Tech. (Mechanical)
· Project Manager – Engineering (Mechanical): 8-10 years experience with a B.E./B.Tech. (Mechanical)
Why Build a Career with TAPI?
Joining TAPI means becoming part of a globally recognized leader in the API space. Employees have the opportunity to work on critical projects that supply essential medicines worldwide, leveraging decades of industry expertise. The company offers a dynamic work environment across multiple strategic locations in India, with roles that promise professional growth and development.
How to Apply?
Interested and eligible candidates who meet the specified experience and qualification criteria are encouraged to share their CVs directly to the recruitment team at TA.India@tapi.com.
The company has explicitly stated that only experienced candidates should apply, ensuring a fit with the technical and regulatory demands of the pharmaceutical API industry.
This expansive hiring initiative presents a prime opportunity for skilled professionals in the pharmaceutical and chemical sectors to advance their careers with an industry titan.
For More Information:
Prospective applicants can review the specific experience requirements for each role and submit their applications to TA.India@tapi.com.
About TAPI:
TAPI is the go-to global supplier for active pharmaceutical ingredients(APIs), supporting the majority of the world’s leading pharmaceutical companies. With a heritage of over 80 years, the company is renowned for its quality, reliability, and extensive portfolio of generic APIs
FAQ:
1. What types of manufacturing technologies and equipment are used in TAPI’s API production facilities?
Answer:
TAPI’s production facilities employ a range of advanced technologies, including continuous flow chemistry, high-pressure hydrogenation reactors, centrifuges, and multi-purpose glass-lined and stainless-steel reactors. The sites also use automated control systems (DCS/PLC) for process optimization, ensuring consistency, safety, and compliance with global GMP standards.
2. How does TAPI ensure regulatory compliance and product quality across its Indian API manufacturing sites?
Answer:
All TAPI sites operate under cGMP (Current Good Manufacturing Practices) and are regularly audited by leading global health authorities such as USFDA, EMA, and WHO. Stringent Quality Management Systems (QMS), validated analytical methods (HPLC, GC, FTIR, LC-MS), and continuous training programs ensure adherence to global regulatory and quality benchmarks.
3. What analytical techniques and instrumentation are commonly used in TAPI’s Quality Control and Analytical R&D departments?
Answer:
TAPI’s QC and AR&D labs are equipped with HPLC, GC, UV-Vis spectrophotometers, FTIR, KF titrators, and Dissolution testers, along with advanced systems like LC-MS and ICP-MS for trace analysis. Analysts routinely perform method validation, stability testing, impurity profiling, and data analysis under ALCOA+ data integrity principles.
4. How does TAPI integrate EHS (Environment, Health & Safety) practices in its operations?
Answer:
TAPI’s EHS framework follows international standards such as ISO 14001 and OHSAS 18001, focusing on risk assessment, hazard identification, and emergency preparedness. Engineering controls, safety audits, waste minimization systems, and real-time emission monitoring are key components of its proactive safety culture. Specialized EHS teams ensure compliance with local and global environmental regulations.
5. What is the role of R&D and Engineering collaboration in process scale-up at TAPI?
Answer:
R&D and Engineering teams collaborate closely during process development and technology transfer phases. R&D establishes lab-scale synthesis and analytical methods, while Engineering designs and optimizes large-scale production systems. This ensures smooth scale-up from pilot to commercial batches, maintaining process robustness, yield efficiency, and regulatory compliance.
