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Analytical Researcher II
Watson Pharama
posted 1mon ago
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Job Description
Select how often (in days) to receive an alert: Analytical Researcher II Nov 18, 2024 Ambernath, India, 421506
Who we are
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
Employment Type: Full Time, Permanent
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Strict timing
Monday to Friday
Within city
Day Shift
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