Job Description

Company Description

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.

Main Responsibilities:

Improve the yield, efficiency, and cost-effectiveness of developed APIs by introducing new technologies and optimizing processes Preparation of various impurities required for quality control department with their characterization data as per CQA guidelines. Involved in new process scale-up, validation, and commercialization activities, adhering to TAPI Technology Transfer policies and regulatory requirements Evaluation and signoff Protocols received from manufacturing. User trial of raw material, intermediates and solvents required to verify new vendors as per the quality assurance guidelines. Establishing the solvent recover and reusability in lab and issue the reports. Generation of safety reports as and when required. Trouble shooting for the plant related problems, to overcome the process related difficulties for smooth production. Support to answer quarries related from customers. To maintain GMP in Lab. Coordinate with other departments from smooth functioning. Develop own skill by way of regarding / attending seminars etc. To maintain discipline and dignity of the organization. Contribute novel ideas by way of participation during technical discussion with superiors/ colleagues. Ensure that local and global EHS KPIs are met without any delay. Conduct Safety GEMBA walks to identify and mitigate workplace hazards. Prepare Nitrosamines Risk Assessments in line with regulatory expectations.

Key Attributes:

Excellent communication skills to interact internally with project teams and externally with customers Retrosynthesis Collaboration and influencing skills to build partnerships with the other disciplines, similar groups, Conscientious with a can-do attitude and thorough attention to detail. Experience in working to GMP. Experience in the application of Process Safety to the design of chemical processes

Key Skills:

Good understanding of Mole eq. calculations Technology Transfer Responsible for End-to-End Life cycle Management Cost reduction Continuous improvement Solvent recovery/recycle

Qualifications

Experience:

4 to 8 Years

Qualification:

M.Sc. (Organic Chemistry)

Additional Information

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!