B.Pharmacy from a recognized institute or with science stream Physics, Chemistry, Biology Approved Diploma In Pharmacy from an institute recognized by the Pharmacy council of India and registered as Pharmacist under Pharmacist Act 1948.
PhD, MD, MPH, M.Sc, Doctor of Pharmacy, Nursing Biostatistics, or any other equivalent Degree with minimum three years of experience in research and teaching
Personnel handling this profile will be responsible for performing reactions as per the requirement of the project. They are also responsible for documenting the observations in relevant note books. They are to follow instructions from the supervisor and work in a group (or individually) to accomplish the tasks in a timely and efficient manner.
Ensure process is in place to maintain the PV QD Training Matrix, training curriculum updated. Ensure global traceability and monitoring of investigations of all identified quality gaps, quality risks and ensure that Corrective and preventive Action Plans are implemented in timely manner.
The Quality Manager responsible for handling technical complaints is tasked with investigating and managing technical complaints raised by clinical investigator sites regarding Investigational Medicinal Products and Medical Devices.
Support data integrity incidents, manage escalations, and contribute to global DI networks and initiatives.
Familiarity with institutional requirements for animal use and welfare in pharmacology experiments is essential. Additionally, you will effectively communicate the goals, protocols, and results, contribute to regulatory submissions, and foster cross-team collaboration to enhance IMA research innovation and decision-making processes.
M.Pharm, M.Sc or in any equivalent field plus minimum of 2 years of experience in the design and development or manufacturing or research or testing or quality in medical device field.