Sr Supv Production

Date:  Jan 21, 2026
Location: 

Goa, India, 403722

Company:  Teva Pharmaceuticals
Job Id:  65223

We are Teva

We’re Teva, a leading innovative biopharmaceutical company, enabled by a world-class generics business. Whether it’s innovating in the fields of neuroscience and immunology or delivering high-quality medicine worldwide, we’re dedicated to addressing patients’ needs now and in the future. Here, you will be part of a high-performing, inclusive culture that values fresh thinking and collaboration. You'll have the room to grow, the flexibility to balance life with work, and the opportunity to better health worldwide, together.

How you’ll spend your day

  • Responsible for upkeep of Granulation area in Production.

  • Responsible for supervising the Granulation area in Production.

  • Preparation and review of SOP’s and other documentation in manufacturing areas.

  • Handling of SAP R/3 system (Manufacturing related transactions).

  • To prepare and review the investigations related to Deviations, OOS, OOT, Market complaints, Exception reports etc.

  • Signing of equipment qualification related documents as a business owner.

  • To review and ensure compliance, calibration, preventive maintenance of all machines in manufacturing areas.

  • Responsible to perform Glorya EDMS related activities.

  • Performing batch manufacturing activities as per BMR instruction.

  • Review of executed batch manufacturing records.

  • Material storage areas management.

  • Ensure Standard Operating Procedure compliance.

  • To comply with the cGMP practices.

  • Undergoing the training as per the identified training needs.

  • Training and utilization of the manpower allotted.

  • Training and development of the manpower allotted in the area to meet the business need.

  • To execute all the tasks assigned by immediate Supervisor/ HOD/ Designee.

  • Responsible for maintaining disciplined work culture in manufacturing area.

  • Management of inspection readiness Program in the Production Department.

  • Participate in the regulatory inspections and internal and external audits.

  • Identification of Shop floor related Improvement Project and implement best Practices in the Production Department.

Your experience and qualifications

  • B.Pharm / M.Pharm
  • 7-10 Years of experience 

How We’ll Take Care of You 

At Teva, better health starts from within, and that includes you. From day one, you’ll be supported with benefits designed to help you thrive in and out of work. This includes generous annual leave, reward plans, flexible working schedules (dependent on role), access to tailored health support, and meaningful ways to give back to the community. 

 

When it comes to your career, you’ll be encouraged to explore, evolve, and shape your path. Twist, our one-stop shop for career development platform, gives you access to a wide range of possibilities, from learning programs and short-term projects to opportunities for internal growth. Here, you’ll be part of a culture that empowers you to reach your goals and prioritize your wellbeing every step of the way. 

 

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.