Conduct chemistry-related testing of entire QC batch.
Maintain and update GMP compliant along with state-of-the-art analytical laboratories.
Coordinate pharmaceutical-related activities for all products.
Evaluate natural plus synthetic materials to identify physical and chemical makeup using different scientific techniques.
Develop relations and coordinate with all colleagues plus compare research.
Prepare, update and maintain reports on basis of scientific deductions.
Develop and present well-structured technical presentations inclusive of R and D reports, quality investigation reports and regulatory filing documents.
Resolve all complex analytical issues inclusive of validation and development of analytical procedures.
Ensure to transfer of new and current products as appropriate.
Interpret all Master Manufacturing Formula documents and perform with production on entire process development.
Ensure to follow cGLP, cGMP and OSHA guidelines with respect to work safety and practices.
Train laboratory staff about usage of analytical and equipment techniques.
Evaluate raw, midway, final product along with stability samples as per given guidelines.
Ensure to qualify, explain and maintain all laboratory equipments.
Write, revise and prepare SOPs as required.