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Analytical R & D Analyst I - TAPI
Watson Pharama
posted 3d ago
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Select how often (in days) to receive an alert: Analytical R&D Analyst I - TAPI Date: Feb 10, 2025
Location:
Gwalior, India, 244235
Company: Teva Pharmaceuticals
Job Id: 60743
Who we are
TAPI is the leading international supplier of active pharmaceutical ingredients (APIs). With the industrys broadest portfolio including over 350 API products. We are the go-to global supplier for APIs, supporting 80% of top 50 global pharmaceutical companies. We are proud of our reliable history in the generic API industry dating back over 80 years, and the fact we are considered to be one of the most trusted API suppliers, these enable TAPI to lead the industry, based on our experience, expertise, technologies, and exceptional customer service.
Our employees are at the core of our success. Our Headquartered is in Israel, TAPI employs more than 4,000 professionals at 14 sites worldwide. Our state-of-the-art production facilities are located in Italy, Hungary, the Czech Republic, Croatia, Israel, Mexico and India. Our significant ongoing investment in R&D generates a steady flow of APIs, enabling timely introduction of new products to market.
Our employees are at the core of our success. Our Headquartered is in Israel, TAPI employs more than 4,000 professionals at 14 sites worldwide. Our state-of-the-art production facilities are located in Italy, Hungary, the Czech Republic, Croatia, Israel, Mexico and India. Our significant ongoing investment in R&D generates a steady flow of APIs, enabling timely introduction of new products to market.
How you ll spend your day
To participate in method development and routine analytical support to pilot and CRD for raw materials, intermediates, in-process samples and drug substance.
Good knowledge of wet chemistry.
Familiar with HPLC, UPLC, GC,GC MS FTIR, PSD, TGA ,KF, Auto titrator and other analytical techniques.
Stability studies and Forced Degradation studies for drug substance as per ICH guidelines.
Calibration and Maintenance of sophisticated Instruments, such as Balance, HPLC, GC, IR, Karl Fischer, Melting point analyzer and Polarimetry.
Conducting routine analysis of CRD and pilot samples as per set procedures.
Documentation as per GMP requirements.
Adhering to safety norms and safe culture in lab.
To ensure online data compilation and recording to have full compliance.
To contribute in maintaining analytical laboratory as per the GLP and safety requirements.
To contribute in providing necessary support to QC during validation batches as well as in routine (Need based in justifiable fashion).
To support in full-filling the regulatory/customer related tasks related to commercial/pipeline products (as per real need and assigned task).
To participate in departmental trainings/discussion programs.
Your experience and qualifications
MSc. in Organic Chemistry/Analytical chemistry
Work Experience: Required: 3-5 years
Already Working @TEVA?
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Teva s Equal Employment Opportunity Commitment
Employment Type: Full Time, Permanent
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Strict timing
Monday to Friday
Within city
Day Shift
Watson Pharama Benefits
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