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.

We're looking for a detail-driven Quality Control (QC) Technician with a strong foundation in GMP/GLP compliance, analytical testing, and audit readiness. If you excel in 24/7 audit preparedness, regulatory documentation, instrument calibration, and hands-on analysis of raw materials, intermediates, and environmental samples, this role offers a dynamic lab environment to thrive in. You'll lead investigations (LIR, OOS, OOT), ensure data integrity, support CAPA training, and drive QC efficiency through meticulous documentation, 5S practices, and cross-functional coordination.

Main Responsibilities:

24 x 7 audit readiness. Participation in internal, external, regulatory audits. Ensure 100% participation in training's against CAPA's. Responsible for initiation and investigation on LIR, OOS, OOT & boarder line results and reporting them to the in-charge. Supporting to share required documents from QC to RA / another requirement. Determining team priorities in accordance with the plant's needs, while coordinating with the team leader/Manger. Follow up the housekeeping, cGMP, GLP and Safety Guideline in laboratory. Sampling, analysis/ planning of RM/PG/intermediates/water/Environment monitoring samples based on requirement and result entry in analytical sheets, QA form and LIMS. Perform analytical test according to the monograph and SOP based on requirement in different shifts (A, B and C). Signing on approved column in data books, laboratory control card and signing on hard copies as well as approval in LIMS based on requirement. Responsible for calibration and verification of instruments. Maintaining of reserved samples room and chambers. Help in preparation of documents related to department (like STP's, SOP's etc.) Ensure the sampling of finished products, Raw material, Intermediate and sending sample to outside laboratory for analysis. Must be ensured sampled, approved and rejected labels timely as required. Responsible for maintaining the stock record of chemicals and reconciliation of standards. Responsible for maintaining safety CAPA. Responsible for maintaining 5-S in QC. Online documentation (based on requirement) must be ensured as per data integrity norms and awareness to team against data integrity. Responsible for support analysis reduction/QC efficiency enhancement programs. Any other job assigned by the Manger -QC Manger or group leader-QC

Qualifications

The ideal candidate will have:

Education:

B.Sc. / M.Sc. in Chemistry

.

Experience:

Minimum

6 years

of 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!