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.
Responsible for In-process production related activities in DP manufacturing, filling, and packing sections. Preparation of batch manufacturing records, process validation protocol/report of DP area and its associated records.
Any M.Pharmacy / MSc (Full time) with 6 to 10 Years (or) B.Pharmacy with 8 to 12 Years of relevant Experience in Manufacturing (Upstream/Downstream) injectables with Strong people management
Review documents required for regulatory submissions across global markets, including product development reports and scientific justifications for responding to regulatory queries.
Bachelors or Masters degree in a field related to Science, Healthcare, Clinical Research or Life Sciences like Biology, Pharmacology, Nursing, or a related discipline.
Centaur Pharma is one of the rapidly growing Pharmaceutical Company in India. To keep pace with our growth plan, we required young and energetic professionals for our Pune site, having experience in Formulation / Oral solid dosage.
To design and conduct experiments for preformulation, formulation optimization of Microsphere and long acting complex non oral dosage form based on QbD approach. To execute the experiments as per Design of experiments