Analytical Scientist

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.
• Laboratory compliance and data integrity during day-to-day operations.
• To prioritize and plan the analytical activities in an effective manner based on the given timeline to facilitate progress of the projects.
• Allocation of daily work based on priorities.
• To guide team members for develop effective analytical methods for developmental projects.
• To have effective coordination between all concerned functions to facilitate timely completion of projects.
• Literature Search for development of analytical methods.
• Review of analytical data generated in the laboratory.
• Prepare analytical method transfer protocol and reports.
• Review of calibration reports.
• Preparation and updation of STP and analytical related SOPs.
• Laboratory resources management.

Your experience and qualifications

• Required M.Sc./ M Pharm/ PhD qualification
• Relevant Experience is 6 to 10 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.