3 – 8 Years
Do literature search and study.
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.
Ensure the compatibility of API and excipients.
Carry out stability and bioequivalence study at each stage of formulations development.
Conduct pilot and pivotal experiments on the PE batch and Exhibit batches respectively.
Compile stability data of previously completed projects.
Maintain lab equipments as per GMP/GLP.
Investigate abnormal results and discuss them with group leaders.
Understand the scalability of the chosen process.
Visualize the developmental needs of the formulation.
Understand the safety and environmental aspect.
Analyze the formulation strategy, efficiency, working relations and cross-functional issues in AR&D.
Calibrate the instruments according to the master calibration schedule and follow GLP and follow SOPs and STP.
Keep the work area clean and the laboratory under controlled temperature.
Maintain the documents well.
Educational Qualifications: M.Pharm/M.Sc.
Experience Required : Minimum 2-6 yrs. experience in Analytical Research & Development (formulations).
Note:Â Minimum of two years of experience in current or previous company is mandatory
Salary: Not Disclosed by Recruiter
Industry: Pharma / Biotech / Clinical Research
Functional Area: Medical, Healthcare, R&D, Pharmaceuticals, Biotechnology
Role Category: Analytical Chemistry Associate/Scientist
Role: Analytical Chemistry Associate/Scientist
Doctorate – Any Doctorate – Any Specialization, Doctorate Not Required