At TAPI, we’re not just a company—we’re a community committed to advancing health from the core. As the world’s leading supplier of active pharmaceutical ingredients (APIs), we partner with 80% of the top 50 global pharmaceutical companies. With a legacy spanning over 80 years and a portfolio of more than 350 products, as well as custom CDMO services, we’re shaping the future of health worldwide.

Our strength lies in our people—a team of over 4,200 professionals across 13 state-of-the-art facilities in Italy, Hungary, the Czech Republic, Croatia, Israel, Mexico, and India. Together, we innovate, solve problems, and deliver excellence. Join us and be part of a mission that transforms lives.

1. Responsible for the validation protocol/report preparation.
2. Responsible for follow up of Validation.
3. Responsible for the study protocols and reports.
4. Responsible for review the deviation and monitor the deviation in track-wise.
5. Responsibility for preparation and support in cleaning matrix/protocols/reports.
6. Responsible for follow up of deviation from plants for conferring the root cause of deviation.
7. Responsible for preparation of investigation report.
8. Responsible for reviewing the investigation report by QA person.
9. Responsible for closer of investigation in track-wise on time.
10. Preparation of manufacturing process batch card through the R&D/Pilot report.
11. Preparation of different type of cleaning batch cards e.g. Product change over cleaning, periodic cleaning, general cleaning etc.
12.  Initiation of change controls in Track wise for manufacturing process/product change over cleaning batch cards.
13. Responsible for upload of manufacturing/Cleaning batch cards in Smart Team.
14. Responsible for follow up of batch cards and cleaning batch cards.
15. Responsible for Initiation of CAPA against investigation.
16. Responsible for follow up of CAPA.
17. Responsible for review the CAPA documents for closer.
18. Responsible for CAPA closer in track-wise on time.
19. Responsible for review of CAPA and deviation of dispatch for on time closing.
20. Responsible for coordinate with plants for query related to track-wise in deviation and CAPA.
21. Responsible for coordinate with dispatch person for smooth dispatch.
22. Responsible for coordinate with batch card preparation team for CAPA implementation in batch card.
23. Responsible for coordinate with engineering department team for CAPA implementation related to equipment's.

Qualification: Bachelor / Master of Science (Chemistry)/ Diploma (Chemical Engineering).

Experience: Minimum 5 Years

Make Your Mark with TAPI

Your journey with TAPI is more than a job—it’s an opportunity to make a lasting impact on global health. If you’re ready to lead, innovate, and inspire, we’re excited to welcome you to our team. Together, let’s shape the future of pharmaceuticals. Apply on top of this page and our talent acquisition team will be in touch soon!