Who we are

Together, we're on a mission to make good health more affordable and accessible, to help millions around the world enjoy healthier lives. It's a mission that bonds our people across nearly 60 countries and a rich, diverse variety of nationalities and backgrounds. Working here means working with the world's leading manufacturer of generic medicines, and the proud producer of many of the products on the World Health Organization's Essential Medicines List. Today, at least 200 million people around the world take one of our medicines every single day. An amazing number, but we're always looking for new ways to continue making a difference, and new people to make a difference with.

Job Description

Human resources management, material and technical resources in order to guarantee compliance with the Production Program, Supply performance, Customer Service based on EHS, Good Manufacturing Practices, Quality System, guidelines, policies, regulations, processes and company rules that contribute to the permanence in the market of our products.

1. Supervise the manufacture of production batches according to the operating procedures, safety, ecology and in order to guarantee the standards of quality and standard performance of the product.

2. Human resource management, material and technological resources to comply with the Production, Supply Performance and Customer Service Program

3. / Plan, program and provide training to the personnel in charge, in order to develop the technical / practical skills of the same, as well as the personal and professional development of the people in their charge.

4.Documenting production processes to comply with the Good Manufacturing Practices, Safety, Ecology and Productivity, contributing to the traceability and quality of the product.

5. / Coordinate activities with areas of MS & T, Quality, engineering, projects and processes for continuous improvement of processes, facilities, design, activities to achieve the objectives of the company.

6. / Actively participate both in the activities and in the supervision of compliance with the safety and ecology guidelines in the modalities of leader or brigadista of the different commissions for the protection of the company's resources.

Your experience and qualifications

Education: /: I.Q., Q.F.B., Q., Q.B.P or similar career, o 5 years of experience developing activities in the production area.

Experience: 2 years of experience at the supervision level of chemical or pharmochemical companies.

Capabilities: / Administration of unionized and technical personnel, operation of reactors, centrifuges, pumps, dryers and equipment related to the manufacture of API's, GMP and Documentation, Security and Ecology, Computing, Brigadist/ Leader, Training.

Language: Intermediate english.

Make a difference with Teva Pharmaceuticals

Reports To

Sr Mgr Section/API Facility

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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.