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.
Job Description
We are looking for a proactive and detail-oriented QC Technician with strong experience in wet lab analytical testing, GMP/GLP practices, and audit compliance. The role involves working in a fast-paced pharmaceutical lab environment with a focus on accuracy, data integrity, and 24×7 audit readiness.
Key Responsibilities
- Perform sampling and testing of raw materials, intermediates, finished products, and cleaning samples as per SOPs, monographs, and testing requirements. Ensure accurate documentation and result entry in analytical sheets, LIMS, and QA systems in line with data integrity standards.
- Conduct routine analytical testing using wet lab techniques and instruments such as Karl Fischer titrator, auto-titrator, analytical balance, FTIR, UV, polarimeter, XRD, and related equipment.
- Handle calibration, verification, and routine maintenance of laboratory instruments to ensure compliance with regulatory requirements.
- Maintain laboratory areas, including reserved sample rooms, chambers, incubators, and autoclaves, along with inventory of chemicals, reagents, and reference standards. Ensure proper storage, labeling, safety, and recordkeeping.
- Support preparation, review, and implementation of SOPs, STPs, and QC-related documentation to maintain audit readiness and cGMP compliance.
- Ensure proper sampling, labeling (approved/rejected), and timely dispatch of samples to external laboratories when required.
- Initiate and support investigations for LIR, OOS, OOT, and borderline results, including root cause analysis, CAPA implementation, and regulatory reporting.
- Ensure continuous audit readiness by adhering to cGMP, GLP, housekeeping, and safety guidelines. Actively participate in internal, external, and regulatory audits.
- Coordinate with cross-functional teams (QA, RA, etc.) to provide required QC documentation and support regulatory needs.
- Prioritize tasks based on plant requirements and collaborate with team leaders to ensure timely completion of activities.
Qualifications
The ideal candidate will have:
- Education:B.Sc. / M.Sc. in Chemistryor B.Pharma
- Experience:5 to 6yearsof industrial experience.
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!
