Collaborate with lab staff to gather study requirements, test article information, and study design details necessary for study initiation, laboratory assignment, and resource planning.
Manage and deliver a wide range of medical writing tasks to a consistently high standard and take the role of Clinical Reporting Project Lead or Medical Writing Lead.
Perform and monitor in-process Quality Assurance activities during the manufacturing process. Responsible to perform line clearance activities in different stages of drug substances manufacturing and Monitoring of cleanroom behavior, aseptic activities, BMR review. Preferred for biological experience.
B.Sc. / M.Sc. / B.Pharm; Knowledge & experience in ointment, cream and topical batch manufacturing. Knowledge of equipment is must for filling lines and manufacturing vessels. Dr.Reddys Lab
Demonstrated ability to operationalize local, EU, and global regulatory expectations into fit-for-purpose bioanalytical plans, including inspection readiness, data integrity, and documentation standards.