Jubilant Generics Limited Hiring 2023 .Jubilant Generics Limited Notification full details below..Interested and eligible candidates can Apply Now.Jubilant Pharma Limited is a global integrated pharmaceutical company offering a wide range of products and services to its customers across geographies. We organise our business into two segments, namely, Specialty Pharmaceuticals, comprising Radiopharmaceuticals (including Radio pharmacies), Contract Manufacturing of Sterile Injectable, Non-sterile & Allergy Therapy Products, and Generics & APIs, comprising Solid Dosage Formulations & Active Pharmaceutical Ingredients.
Vacancy details:
- Post Name: Executive-Pharmacovigilance
- Qualification: Post Graduate Life Sciences/B.Pharm/Equivalent
- Experienced: 0-2 years in Pharmacovigilance/Pharma industry/clinical research and/or drug safety
Job Description: Greeting from Jubilant Generics Limited !!!!
Important Details :
- Location: Greater Noida, Uttar Pradesh, IND
- Selection Process: The selection will be on the basis of Interview.
Job Context: To ensure prompt and adequate reporting of suspected adverse drug reactions in line with current regulatory requirements, together with customer enquiries.
Challenges: To be responsible for assisting management of all local Pharmacovigilance systems to ensure regulatory compliances.
Principle Accountabilities
Case processing / data entry and related activities in the Argus safety database as per DE conventions within specified timelines.
Participate in downloading, triaging, uploading and book-in of regulatory and EMA MLM ICSR reports.
Participate in triaging and book-in of literature reports.
Triage, Case book-in, data entry & archiving.
Ensure use of PV-MedDRA for coding adverse reactions
Documentation
Ensure that pharmacovigilance SOPs, procedures, processes, and guidelines are adhered to communicate with external and internal customers in a timely manner, as per the requirement.
Statutory Compliances
Maintain an awareness of current legislation associated with the Worldwide Regulatory Pharmacovigilance requirements.
Ensures regulatory compliance by providing timely, quality information for aggregate reports and signal review following SOPs and regulations.
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