Company Jobs

BS degree in Pharmacy or Life Sciences or relevant education. Minimum 1 year of relevant experience in regulatory affairs, quality or product development in the pharmaceutical, medical devices or similar FMCG industries.

Identify and execute appropriate workup and purification technique to produce an intermediary / final compound of desired quality

The objective of the role is to perform chemical synthesis of molecules, the role involves process development, process validation and transfer to production units.

Support business partners in assessing brief submitted by project sponsors for each new project. Identify any gaps and missing information to be collected with the sponsor.

Candidate should be science Graduate having good communication skills.

Responsible for discussion and planning strategies for product development, executing them and recording them in E-Lab notebook. Identify and proactively discuss potential challenges along with possible way forward.

OSD-coating, Compression, Packing, Granulation, Ointment-External Preparation (General & Sterile Manufacturing). Injectable (Aseptic, SIP, CIP, Batch Manufaturing, Bulk Manufacturing, Dry Powder), Oral Liquid

Review of drafts includes checking content pieces developed by other team members for clarity, perspective, accuracy, appropriateness for target audience, and overall quality, in line with all applicable guidelines and internal checklists.

Preparation, review and submission of Dossiers, Good exposure on Life Cycle Management. Handling Post approval & Pre approval