B.Sc

B.Sc./ M.Sc./ B.Pharm / M.Pharm. Manufacturing / Packing, Quality Control, Quality Assurance. Exposure to OSD Manufacturing operations like Granulation, Compression, Coating, Pellet coating, Capsule filling, Primary Packing and Secondary Packing. Working in USFDA Plant.

M.Sc/ B.Pharm / M.Pharm. To plan, prepare and review of high quality dossier with support and guidance, assuring technical concurrency and regulatory compliance, meeting agreed upon timeline.

M.Pharm, B.Pharm, M.Sc, B.Sc, ITI, Diploma; Experience Into Analytical Validation. Finished Goods. Raw Material. Stability & CLP

M.Pharm. Exposure in EU/ US/ UK/ ROW market. Formulation patent exposure. Strong communication skills, Problem-Solving, & Adaptability.

Preparing eCRF specifications, Edit check specification and other study specific set up documents.

Should be well-versed with techniques such as Spraytech, and Sprayview8t Pattern, Pump delivery test also good working knowledge of HPLC. 

Bachelors degree in chemistry, toxicology, product stewardship, industrial hygiene or related discipline required

You will be responsible for preparation, review, and approval of Cleaning Master Validation Plan, Cleaning Validation and Verification Protocols and Reports, Acceptance Criteria documents, Cleaning Validation matrix, and Periodic Monitoring Schedule

Degree in Pharmacy from an Institute / University recognized by All India Council of Technical Education. Public Service Commission