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
- Receipt, registration and upkeep of all the samples in the laboratory.
- Perform sampling of water and compressed analysis as per plan to adhere to the schedules and meet priorities.
- Analysis to be performed based on qualification matrix of the analyst for MLT, environmental monitoring, water testing chemical, media preparation, growth promotion, compressed air testing etc.
- To perform microbial suitability testing for the new materials / product.
- Timely and error free documentation as per the GLP requirement.
- Calibrations of Laboratory Instruments and Equipment.
- Used media decontamination after reporting the observations.
- Revision and updation of Standard Operating Procedures, test methods and specifications.
- Maintenance of media, biological indicator and Gastec tubes etc.
- To ensure compliance to the requirements of policy and procedures on Data Integrity.
- Timely reporting of Out of Action/Alert Limits, OOT, Trends, Deviations and LIR (If any).
- To maintain the assigned Laboratory workplace, instruments, and equipment.
- To ensure timely disposition of analytical samples.
- To ensure that the analysis is Right first time and activity completion as per committed timeline.
- Trend preparation for the water, environmental monitoring and summary preparation for compressed air.
- Ensure timely completion of assigned trainings.
- Active participation in regulatory Audits.
Your Experience And Qualifications
- BSc/MSc in microbiology/Degree in Biotechnology
- 1-3 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.Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, genetic information, marital status, sexual orientation, gender identity or expression, ancestry, national or ethnic origin, citizenship status, military status or status as a disabled or protected veteran, or any legally recognized status entitled to protection under applicable federal, state, or local laws.
