Job Description

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

• 24 × 7 audit readiness.
• Experience of Wet Chemistry.
• Responsible to works in different shifts.
• 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/ other requirement.
• Determining team priorities in accordance with the plant’s needs, while coordinating with the teamleader /Manger.
• Follow up the housekeeping, cGMP, GLP and Safety Guideline in laboratory.
• Sampling and analysis of RM / FG / intermediates / cleaning samples based on requirement and result entry in analytical sheet, QA form, LIMS and online documentation as per data integrity norms.
• Perform analytical test according to the monograph and SOP.
• Responsible for calibration and verification of instruments.
• Maintaining of reserved samples room and chambers / autoclaves / incubators.
• Help to in charge in preparation of documents related to department (like STP’s, SOP’s and 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 to maintain the stock record of chemicals and reconciliation of standards.
• Any other job assigned by the Manger -QC Manger or group leader-QC

Your experience and qualifications

• Bachelor/Master of science (Chemistry)
• Minimum 3 years

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.

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