Description:
Roles & Responsibilities :–
Working on Formulation & Development of dosage forms like Oral Solids (Tablet & Capsules)&ndash IR tablets, Sustained release tablets, extended release tablets, Bilayer tablets, Capsule etc. & External preparations like Gels, Pastes, Creams, Ointments etc. under guidance of consultant.
Working under guidance of consultant, to plan of work to meet regulatory market compliances as per QbD guidelines.
Performing Literature search and conducting the pre-formulation studies under consultant&rsquos guidance.
Planning and organising day-to-day research activities & performing quality scientific experimentation as per Consultants design. Taking Consultants guidance to resolve any procedural problems as appropriate to the timely completion of research objectives.
Properly documenting activities of the project under investigation under guidance of consultant. Preparation and Review of document like Product Development Report, Master Formula Card and Batch Manufacturing Record, product development report as per ICH, USFDA guidelines under consultant&rsquos guidance.
Coordinating & continuous follow up with various departments like analytical development, purchase and store.
Working under guidance of consultant for Execution of Scale up batches and Pre-Exhibit batches.
Preparation and Review of document like CQA, QTPP, CPP and BOM.
Initiating Change Control for scale-up batches.
Supporting the activities of the R&D Department, including safety performance, employee relations and quality.
Highest Qualification :–
M.Pharm
Location :–
Akola
you can mail your resumes on [email protected]