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.

The opportunity

• Finished product testing and analytical method development by HPLC, GC, IC, UV etc.
• Analytical method validation and transfers, analysis of API, Finished product R&D samples

How you’ll spend your day

• Analysis of Solid oral dosage i.e. Dissolution, Assay, CU, BU and Related substances etc.
• Analysis of samples received from Formulation department (samples include in-process, finished product, pre-formulation study samples and stability samples etc.).
• To carry out analytical method development and method validation, in-process samples and finished products.
• To carry out analytical method transfer activity to QC, Goa.
• Handling and testing of hi-potent compounds/molecules
• Trouble shooting of analytical instruments for difficulties faced during day-to-day operations.
• Calibration and maintenance of analytical instruments. Maintenance includes activities such as Qualification, keeping track of AMC, History, Spares, Usage records etc.
• Literature Search for development of analytical methods.
• To ensure that all activities undertaken are executed in the framework of good laboratory and documentation practices and the existing quality systems are adhered.
• To ensure safe practices are followed during the execution of activities and strict adherence to the EHS systems of the site.

Your experience and qualifications

• M.Sc. / M. Pharm./ Ph. D
• 3-8 Years relevant experience
• Sound knowledge of Chemistry and analytical method development, method validation and transfer, Instrumental method of analysis and logical approach.
• Hands on experience on Instruments viz., GC, HPLC, Ion Chromatography, UV and Dissolution apparatus etc.
• Knowledge of regulatory requirements for different markets (US, EU, Canada etc.
• Knowledge on ICH guidelines, forced degradation studies, impurity profile etc.

Personal attributes

• Basic communication skills
• Must be honest and trustworthy
• Be respectful
• Possess cultural awareness and sensitivity
• Outgoing, personable, responsible, self-motivated and confident

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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