For Research & Development

• Conduct pre-formulation study for method development
• Perform analytical method development activities of Raw Material & Finished products
• Conduct formulation activities for new & existing products and its registration activities as per WHO & DGDA regulatory norms
• Ensure the trouble-shooting activity of the products to solve any product problem by maintaining compliance with quality
• Raise Document initiating form Change Control Report (CCR), Change Document Report (CDR), Handling of Deviation and perform risk assessment as per requirement
• Prepare Process Optimization (PO), Process Validation (PV) documents like protocol, batch documents etc. and conduct the PO and PV Batches as per procedural requirement

For Production

• Monitor and ensure the manufacturing process as per planning, guidelines & Standard Operating Procedure (SOP) to ensure in-time production
• Ensure cGMP compliance in all production activities
• Prepare Batch Manufacturing Records (BMR), Batch Packaging Records (BPR) and other documents
• Supervise & provide training to the Operators, Helpers and other Production Workers
• Monitor productivity on daily, monthly as well as yearly basis

• M.Pharm / B.Pharm (Professional)
• 1-2 years experience in related work in reputed pharmaceutical company is preferable but fresh candidates are also encouraged to apply
• Good interpersonal and communication skills
• Candidate must possess excellent planning & execution skills as well as strong quantitative & qualitative analytical skills
• Well conversant with MS Office
• Within 30 years of age

Only short-listed candidates will be called for further hiring process and hard copy of CV will not be entertained.

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