Dr Reddy’s Laboratories Ltd Job Vacancy for Process R&D Scientist/ Formulation Scientist - OSD
PROCESS R&D SCIENTIST -API (FEMALE)
Experience: 3 to 8 yrs
Location: Hyderabad
Job Description
Selection/Designing non-infringing, cost effective and scalable synthetic routes by thorough review of journals and patents.
Identify and evaluate the reaction parameters. Study the Process Feasibility, Process Optimization, Lab Validations and Technology Transfer to plant.
Understand underlying science and fundamental concepts behind the product development. Robust process development skills are desirable.
Keeping up to date with relevant scientific and technical developments. Execute experiments efficiently with high reproducibility.
Interpretation of analytical and spectral data to ensure quality and compliance (HPLC, GC, IR, NMR, XRD, DSC, TGA and other analytical methods)
Write technical development reports, QbD reports, justification reports and DMF filing related documents. Ensure full documentation compliant (GMP) with R&D quality procedures.
Provide support in scale up batches execution and ensure process reproducibility at scale.
Ensuring lab safety and process safety is mandatory.
Note : Kindly Share CV to bchakradhar@drreddys.com
FORMULATION SCIENTIST – OSD
Job Description:
Formulation development activities:
Pre-formulation activities, design and execution of formulation trials, getting the samples analysed and interpret the results. Discuss with superiors on further plans and execution of trials IN ORDER TO get stable and bio equivalent product.
Strategize and propose formulation approaches for product development in order to meet target product profile.
Search and review scientific information / literature for on-going and up-coming projects in order to run and generate programs (projects on innovative medicine) for business.
Identify and propose formulation strategy for product development.
Read, discuss with superiors and derive the technology, innovation, commercial scale-up feasibility and criticality/complexity IN ORDER TO make proposal drafts and initiate formulation development for assigned project.
Visualize the developmental needs of the product.
Carry out pilot experiments and finalisation of stable , robust formulation for bio studies.
Support to supply manufacture for clinical trials and execution of registration batches.
Understand the safety and environmental aspect.
Understand the scalability of the chosen process.
Knowledge on Risk Assessment and QbD development .
Execute & ensure proper Pilot bio batches as per GMP requirements.
Understanding of good In vitro -In Vivo relations.
Proper risk assessment at different strategy of development.
Proactive working and be prepared for different phase gate meetings.
Specification preparation for RM, FP, Stability specifications.
Ensuring proper licences and Raw material in advance manner.
Co-ordination with cross-functional teams:
Drafting, submitting applications with all necessary information to RA for related Lics; and material procurement with SCM for smooth functioning in product development.
Work along with Cross functional team towards project milestones as per timelines
Documentation:
Maintaining the documents well.
Compilation of conclusive data (formulation and analytical) for individual project as a Product Development Report IN ORDER TO summarize product development for further technical and commercial decisions.
Misc. Lab function:
IQ/OQ/PQ of new equipment and instrument, daily and scheduled calibration of lab instruments/ equipments, procurement of lab consumables IN ORDER TO ensure fully operational level for different projects
Interested Candidates Can share their
CVs to the given mail ID: Chintalapatikavya@drreddys.com
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