Quality Control Analyst II- Microbiology
Date:
Jul 15, 2025
Location:
Goa, India, 403722
Company:
Teva Pharmaceuticals
Job Id:
62807
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
- To ensure receipt, registration and upkeep of samples in the laboratory.
- To complete review of microbiological testing reports related to (but not limited to) raw materials, finished products, stability
- study samples and Hold Time Study samples, water testing, microbial method validations and environmental monitoring.
- To ensure timely review and release of the report and submission to the respective section.
- Maintain GLP compliance, inspection readiness and best microbiology practices.
- To maintain laboratory workplace, instruments and equipment.
- Review of records related to microbial media preparation, sterilization, GPT, media reconciliation garment sterilization.
- Review of documents related to Temp and RH, Pressure differentials, UV, incubator cleaning and temperature data and area
- cleaning and sanitization and fumigation.Review, locking and usage decision of water reports entered in SAP.
- To ensure timely completion of laboratory instrument/ equipment’s and review of electronic records.
- To ensure timely disposition of balance analytical samples and expired media.
- To ensure readiness of water and Environmental monitoring trend and Summary report and Summary report of compressed air.
- Reporting and investigation of Deviations, Out of Action/AIert Limits and LIR in the laboratory.
- To ensure timely/ periodic revision of Quality Control Procedures, Standard Test Procedures, Specifications, Standard operating procedures and Glorya related activities.
- To support in facility qualification in coordination with the engineering and manufacturing for new area, area modification, water system, compressed air system for Microbiology section related activities.
- Timely closeout and effective implementation of CAPA assigned by different sections and identified during investigation of quality documents.To ensure compliance to the policy and procedures requirements on data integrity.
Your experience and qualifications
- M.Sc Microbiology
- 12+ 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.
