Job Description

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 maintain Good Laboratory Practices in the laboratory.
• To maintain the assigned Laboratory workplace.
• Timely analysis and reporting of finished products/stability study and ancillary item, to adhere to Production schedule and SOP instructions
• Maintenance of test procedure of raw materials and ancillary item.
• Responsible for sending samples to external laboratory.
• Vendor approval sample analysis.
• Hands on the techniques / SOPs / instructions to be followed up as per the good laboratory Practices.
• To participate in Method transfer and validation activities as per committed timelines of New Project.
• Reporting of Laboratory Investigation of OOS, OOT, Action Limit and Aberrant Analytical Test results, Chromatographic errors, and Deviations (If any).
• Responsible for maintenance and upkeep of Sample storage area.
• Exposure to authorized regulatory audit agencies, e.g. USFDA, MHRA etc.
• ANDA – regulatory submission awareness / basic knowledge.
• Ability to have a learning ability / troubleshooting experience on newly developed products.
• To ensure timely disposition of samples.
• Calibration of laboratory instruments.
• Any other responsibilities given by Section-Head.

Your experience and qualifications

• Bsc or Msc in Chemistry
• 3 to 10 years relevant experience in Quality Control Laboratory

Reports To

Lead Analytical Scientist- Solid Oral Dose - India

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.

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