Supv Production - Compression
Date:
Aug 5, 2025
Location:
Goa, India, 403722
Company:
Teva Pharmaceuticals
Job Id:
63160
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.
How you’ll spend your day
- Responsible for upkeep of Compression area in Production.
- Responsible for supervising the Compression 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.
- To initiate, review and impact assessment of Quality management systems as part of investigation such as Change controls, CAPAs, Risk assessment 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.
- Documentation of all activities in areas worked.
- Daily production planning and execution.
- Coordination with cross functional departments for smooth functioning of production activities.
- 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.
- To follow the normal safety precautions in production department.
- Responsible for maintaining disciplined work culture in manufacturing area.
- To ensure readiness of the department for regulatory inspections and ensure their compliance.
- 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.
- To ensure compliance to data integrity as per laid down system and procedure.
Your experience and qualifications
- B. Pharm / M. Pharm
- 6+ years of experience
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.
