November 2024

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. 

Diploma in Mechanical, Electrical & Pharmacy. Candidates must clear technical and English proficiency tests.

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.

12th Pass in Science subject and Diploma in Pharmacy from a recognized Institution, Board. Experience in dispensing and, or storage and dispensing of drugs in a reputed hospital or institution or in a drug store or a pharmaceutical concern.

Applications are invited on a plain paper for the contractual post of Junior Materiovigilance Associate under NCC-MvPI, IPC Regional centre, Department of Pharmacology, PGIMER, Chandigarh-160012. Masters in Pharmacy, Biomedical Engineering and Clinical Engineering.

Post Graduation in Science M.Pharm, Life Sciences, Biotech, Zoology, Botany, etc. PG Diploma in Clinical Research mandatory. One year of experience as Clinical Trial, Research Coordinator is required.