TAPI - QC Operation Laboratory Manager

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. Headquartered 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. Main Responsibilities And Activities In the QC Department, we are looking for a brilliant profile reporting to the QC Manager with the following responsibilities and activities: Use the StarLims in order to perform all the approval activities related to system management; in particular: tests approval, monographs approval, clients approval, stability protocols/studies approval, analytical sheets approval. Use the TrackWise system in order to manage/approve the laboratory investigations/deviations. Use the TrackWise system in order to manage/approve the CCM records. Act as QC manager backup in TrackWise, Smarteam and LIMS systems. Manage the practical activities of the department in order to ensure compliance with xGMPs, regulatory guidelines / Divisional Policy etc. Collaborate with the department manager in the issuance of analytical control procedures following reclamation activities. Support the department manager during audits and inspections (internal and external). Ensure compliance with safety regulations in the department. Coordinate a Group Of Supervisor And Lab Analysts Support Supervisors and, if necessary, Laboratory Analysts, in laboratory investigations (LIR, OOS, complaints) and in the implementation of effective CAPAs. Support the Supervisors in planning the activities of the department. If necessary, replace the Supervisor in the review and approval of the analytical work. Review and approve the laboratory activities necessary for its maintenance (eg, instrumental requalification, periodic checks, daily calibrations). Represent the practical contact point for the other departments of the Site. Collaborate in the organization of internal professional refresher courses. In line with the policies of the Human Resources department, ensure the motivation and development of employees, intervening with appropriate managerial actions where necessary. Requirements Education: University degree in Chemistry, Pharmacy or CTF Skills Ability to work cross-functionally Familiar with Quality IT Systems Experience in Inspection management Languages English and Italian (level of proficiency) Minimum Experience / Training Required Minimum: 4 years work experience in Quality Control What we offer? We try to take care of our employees, offering them small and large benefits. By way of example: Canteen Working flexibility for Caregivers and parents Coffee Key Recognition Program Welfare Platform Health agreement with medical centers of excellence Highly inclusive and multicultural working environment Continuous learning and development programs (with full access to Linkedin Learning) Type of contract: long term contract Location and working program Santhià (VC), from Monday to Friday Teva's commitment to equal opportunities Teva is committed to equal opportunities in the world of work. Our global policy requires equal employment opportunities to be provided regardless of age, race, religion, health, identity, gender expression, protected categories, or any other legally recognized status that is entitled to protection under applicable laws. J-18808-Ljbffr

Location: santhià, IT

Posted Date: 4/7/2025