Analytical Researcher I

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

• Development of Analytical methods by HPLC, GC, IC, UV etc.
• Development of analytical methods, analytical method transfers, analysis of 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, in-process samples and finished products.
• To carry out analytical method transfer activity to QC, Goa.
• 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.
• Laboratory compliance and data integrity during day-to-day operations.
• Literature Search for development of analytical methods

Your experience and qualifications

• M.Sc. / M. Pharm qualified
• Relevant experience - 4 to 8 years
• Sound knowledge of Chemistry and analytical method development, Instrumental method of analysis and logical approach.
• Hands on experience on Instruments viz., GC, HPLC, Ion Chromatography, UV and Dissolutions 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

Reports To

Group Leader/ Manager

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.