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 Good understanding of GMP documentation. Preparation of SOP / schedule for Equipment/ Facility as per GMP documentation of API plant. Preparation engineering deliverables including Specifications, Datasheets, PM schedules etc. Responsible for GxP documentation i.e. Change initiation, DQ, SAT, IQ, OQ. Understanding and ensuring quality compliance with cGMP, GDP, GEP,GAMP, 21 CFR part 11 Good in computer skills and preparation of daily/monthly excel reports, work power point presentation and using of industrial software i.e. Priority. Handling complete mainatence module for preventive/ breakdown/productive maintenance of equipment’s. To use the problem-solving tools to find out the root cause of any failure and implement the CAPA accordingly. Expertise in problem Solving tools to find out the root cause of any failure and implement the CAPA. FMEA, Root cause analysis, with in depth knowledge about the latest Maintenance techniques and CI tools-5S, Kaizen, 5 why Analysis, RCA, CAPA. Preparation of investigation report and CAPAs. Tracking and implementation of GxP and EHS CAPA. Tracking and maintaining of down time of site related to engineering. Maintaining all documentation for engineering department. Maintaining statuary & regulatory compliance for department. Responsible for spare part management for engineering department. Preparations of budget requirement for engineering department. Tracking of departmental budget to maintain the allocated budget. Responsible to carry out the preventive maintenance of cGMP equipment, critical equipment and its subparts etc. as per schedule. Your experience and qualifications B.E. / B.Tech(Mechanical/Chemical) Minimum 7+ 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.