Quality Control Technician II - TAPI

Who we are

TAPI is the leading international supplier of active pharmaceutical ingredients (APIs). With the industry's broadest portfolio including over 350 API products. We are the go-to global supplier for APIs, supporting 80% of top 50 global pharmaceutical companies. We are proud of our reliable history in the generic API industry dating back over 80 years, and the fact we are considered to be one of the most trusted API suppliers, these enable TAPI to lead the industry, based on our experience, expertise, technologies, and exceptional customer service.

Our employees are at the core of our success.  Our Headquartered is in Israel, TAPI employs more than 4,000 professionals at 14  sites worldwide. Our state-of-the-art production facilities are located in Italy, Hungary, the Czech Republic, Croatia, Israel, Mexico and India. Our significant ongoing investment in R&D generates a steady flow of APIs, enabling timely introduction of new products to market.
 

How you’ll spend your day

1. 24 × 7 audit readiness.

2. Exposure in Wet Chemistry.

3. Responsible to works in different shifts.

4. Perform the raw material analysis & wet lab activity by using the technique (KF, pH, KFC, UV, FTIR, SOR, Oven, Auto titrator, Polari meter & TLC) etc.

5. Sampling of Raw material / FG / intermediates / cleaning samples based on requirement and result entry in analytical sheet, QA form, LIMS and online documentation as per data integrity norms.

6. Perform analytical test according to the monograph and SOP.

7. Follow up the housekeeping, cGMP, GLP and Safety Guideline in laboratory.

8. Participation in internal, external, regulatory audits.

9. Ensure 100% participation in training’s against CAPA’s.

10. Responsible for initiation and investigation on LIR, OOS, OOT & boarder line results and reporting them to the in-charge.

11. Determining team priorities in accordance with the plant’s needs, while coordinating with the team leader /Manger.

12. Responsible for calibration and verification of instruments.

13. Maintaining of reserved samples room and chambers.

14. Must be ensured sampled, approved, and rejected labels timely as required.

15. Responsible to maintain the stock record of chemicals and reconciliation of standards.

16. Any other job assigned by the Manger -QC Manger or group leader-QC

Your experience and qualifications

• M.Sc. / B.Sc. Chemistry

• 5+ Years (Pharma API Industry)

Already Working @TEVA?

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Teva’s Equal Employment Opportunity Commitment

Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's global policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws. We are committed to a diverse and inclusive workplace for all. If you are contacted for a job opportunity, please advise us of any accommodations needed to support you throughout the recruitment and selection process. All accommodation information provided will be treated as confidential and used only for the purpose of providing an accessible candidate experience.