Sr Mgr Section/API Facility

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 opportunity

• To prepare review, approve and distribution the instruction for the production of intermediates and /or APIs according to written procedure.

• To Ensure that all production deviation are reported and evaluated on time, critical deviation are investigated and the conclusion are recorded as per the standard procedure.

• Ensures that all work carried out is in compliance with the required standards conforming to company – e.g. cGMP, SOP, Health and Safety and Environmental requirements.

• Responsible for training and qualification of plant personnel and ensures that the required training is carried out and adapted according to need;

• Leads, staffs, and develops a motivated, skilled and optimally resourced team to ensure that performance levels and professional development achieve or exceed business objectives;

• Act as qualified trainer of those with less experience. Conduct in-direct supervision of others in the team

How you'll spend your day

• Provides input into annual performance evaluations of production technicians as applicable. Investigate and resolve problems. Clear and concise communication to Process Lead and Supervision

• Extensive equipment knowledge to perform trouble shooting and root cause analysis. Develops solutions to complex problems requiring resourcefulness and creativity/innovation and ensures solutions are consistent with organization’s objectives.

• As an Opex champion, identification of improvements projects in respective area and supporting functional head to implement the project

• Extensive Knowledge of Documentation in the Pharmaceutical industry related to process & cleaning validation, DHT, CHT , Cleaning Verification etc.

• Extensive Knowledge to carried out investigation of any OOS/OOT/ Deviation with proper tools.

• Coordination with the cross functional teams including Global teams(EHS, RA, R&D, SCM etc.) to provide accurate approach for the Implementation

• Estimate base line performance and implementation of OPEX in respective area to achieve the targeted continuous improvement in cost, quality , compliances and EHS.

Your experience and qualifications

B.Tech / B.E (Chemical) : 15 to 22 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.