1st class Post Graduate Degree, Including the integrated PG Degree in Life Sciences Or 2nd Class Post Graduate Degree, Including the integrated PG Degree with PhD in Life Sciences
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.
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.
M.Tech / M.S (Pharm) / M. Pharm / MSc in Pharmacy / Nanotechnology from a recognized University with sound knowledge in the application of nano formulations in drug delivery plus GPAT/GATE/NET/ any national- level entrance test, qualified
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.
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.
Granules India is a vertically integrated, high-growth pharmaceutical company with 38 years of proven performance and increasing performance and increasing presence across the world.
Execution QA comprehensively reviews rendering quality, Metadata, Content Matrices accuracy with the email build, Subscriber segmentation, Journey configurations, and deployment accuracies. Calls out and communicates all inconsistencies to Campaign Managers and Deployment teams.
Preparation of documents and facilitation of documentation management in R&D while following established guidelines for correctness, completeness and clarity.
The role is responsible to asses / audit Sun manufacturing sites against current regulatory expectations / standards to ensure regulatory compliance. It includes adhering to applicable regulations, as well as Sun Pharma's policies and procedures.
Analytical Method Transfer of various pharmaceutical dosage forms like oral solid, oral liquid, Injectables, Nasal Spray. Analytical method development and validation for pharmaceutical dosage forms.