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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