Dr.Reddy's Scientist - Analytical R&D - API
Reporting To: Sr. Tech Lead - API
Location: IPDO, Bachupally, Hyderabad
Key Responsibilities:
- Review relevant literature.
- Genotoxic Impurities quantification method development by
using the chromatography.
- To work on the regulatory deficiency queries.
- Qualification of reference standard/working standards.
- Develop analytical methods, conduct validations of these
methods and transfer method to QC.
- Prepare Method Development and Method Validation reports.
- Compile forced degradation & identification of unknown
impurities.
- Do online sample analysis for product development.
- Compile stability data of previously completed projects.
- Analyze the product strategy, efficiency, working
relations and cross-functional issues in AR&D.
- Visualize the developmental needs of the product.
- Understand the scalability of the chosen process.
- Procure chemicals, solvents, columns, etc.
- Maintain lab equipment's as per GLP.
- Investigate abnormal results and discuss them with group
leaders.
- Understand the safety and environmental aspect.
Calibrate the instruments according to the calibration
schedule and follow GLP and SOPs.
- Keep the work area clean and the laboratory under
controlled temperature.
Maintain the documents well
Key Attributes:
- Self-starter, able to work independently with minimal
supervision
- Good communication and writing skills
- Learning aptitude to learn and understand analytical
Operating Network: Product Development Teams, Plant QA/QC
teams, Regulatory Teams, Manufacturing teams etc
Educational Qualifications:
M.Sc Chemistry / B.Pharm / M.Pharm
Experience Required: 2-4 years of experience in QC
Validations, API
Email: tatipdo@drreddys.com
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