Dr. Reddy's Lab
Work as Team Member–TTG (Analytical-Method development)
Established in 1984, Dr. Reddy's Laboratories (NYSE: RDY) is an emerging global pharmaceutical company with proven research capabilities. The Company is vertically integrated with a presence across the pharmaceutical value chain. It produces finished dosage forms, active pharmaceutical ingredients and biotechnology products and markets them globally, with focus on India, US, Europe and Russia. The Company conducts research in the areas of cancer, diabetes, cardiovascular, inflammation and bacterial infection.
To perform and monitor Analytical trouble shooting, Method development, method transfers and other related activities for TTG analytical Academic Having in depth knowledge on analytical methods, instrumentation and calibrations.
•Well versed with analytical instrumentation like HPLC, GC, Dissolution, UV, IR spectrophotometers etc.
•Should have sound knowledge on instrumentation and wet analysis principles.
•Should have hands on experience on development and analysis of various dosage forms.
•Should have experience and capable of online documentation and monitoring lab compliance.
•Should have good knowledge of cGMP and cGLP and other regulatory guidelines such as ICH etc.
•Analytical method development,
Trouble shooting and related analysis.
•dentify, justify and implement method improvements/modifications, OOS/OOT investigations
•Analytical method validation
•Study and interpret analytical and related documents such as DMF open parts, patents, STPs SOPs etc.
•Preparations of equivalency reports, transfer protocols & reports, stability protocols & reports etc.
•Maintenance of lab compliance such as calibration schedules etc, preparation of SOPs and other documents.
Key performance Indicators:
•Number of method developments/improvements.
•Number of validations.
•Addressing trouble shooting through root cause analysis.
•Contribution to AVDs
•Identification of potential threats in routine analytical practices and resolving.
Key personal attributes:
•Should have good communication & interpersonal
•Ability to work with cross functional teams
•Should be good team player, patient and listener
•Should have positive attitude and Analytical thinking and innovative thinking for trouble shooting.
•The position shall work at shop floor of different plants and interact with different departments like Supply chain, Production, QC, QA, RA etc.
•The position also needs to work with other companies.
•Should be M.Pharm ( Pharmaceutical chemistry, Pharmaceutical analysis)/ MSc (Organic, analytical)
•4-6 years of experience in Analytical method development / Analytical method validation.
Experience: 4-6 Years
Functional area: Healthcare, Medical, R&D
Industry Type: Pharma/ Biotech/Clinical Research
Business Unit: FTO Unit II
Reference Code: C 236