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
-
To support the Global R&D sites for Nitrosamines related Projects
-
Executing the routine analytical activities such as Method Development, Method validation and Method Transfer activities related to Nitrosamines Impurities and other various tests for API, intermediate products and finished products R&D samples under the guidance of supervisor.
How you’ll spend your day
- To execute the daily analytical work based on allocation and priorities related to the Nitrosamines impurities in an effective manner based on the given timeline.
- Handling and reconciliation of Global analytical samples received from In-house FRD & different Teva Sites.
- Compilation of analytical data generated in the laboratory data strictly adhering to the Quality compliance and in accordance with GLP.
- Support the team in maintaining the prerequisites for Laboratory such as Column, Standards, Chemicals, Spares and Consumables etc.
- To ensure that all activities undertaken are executed in the framework of GLP practices as well as good documentation practices and the existing quality systems are adhered to.
- Support in preparing various Laboratory Documentations such as STPs and analytical related SOPs etc.
- Trouble shooting of analytical instruments for difficulties faced during day-to-day operations.
- Executing the daily Instrument calibration activities
- Laboratory compliance and data integrity during day-to-day operations.
- Actively participate in the implementation of EHS system/Policy. To ensure safe practices are follow during the execution of analytical activities and strict adherence to the EHS systems of the site.
- Literature Search for development of analytical methods
Your experience and qualifications
- MSc./M. Pharm/ Analytical Chemistry
- Masters with 6-9 years relevant experience OR Ph.D. with 3-6 years relevant experience in Analytical Chemistry especially in Analytical method Development & Validation for Nitrosamine Impurities in Drug Substance and Drug Product and logical approach.
- Hands on experience on advance Mass technology such as LCMSMS, GCMSMS, LC-HRMS etc.
- Knowledge of regulatory requirements for different markets (US, EU, Canada etc.)
- Sound knowledge of pharmaceutical Quality System, ICH guidelines etc.
Personal attributes
- Basic communication skills and ability to work in a matrix structure
- Must be honest and trustworthy
- Be respectful, Possess cultural awareness and self-motivated
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.
