\ \ Job Title Manager Regulatory AffairsIndustry PharmaWork location NoidaExperience required 8+ yearspackage upto 10LPAJob Description:Manager Regulatory Affairs having experience of at…
\ Job description:Roles and Responsibilities: Ensure timely authoring and submission of dossiers (Module 2 5) for regulated and ROW in the eCTD…
MEDICAL REPRESENTATIVE (ASSOCIATE) FOR A FASTEST GROWING PHARMACEUTICAL COMPANY FROM BANGALORE FOCUSING ON GASTROS,SURGEONS,GYNAE AND PHYSICIAN. Relationship Building : Build and maintain…
Experience: 10+ years of experience including team handling experience in similar domainLocation: Ahmedabad, GujaratSummary of Profile specifications:Incumbent should have sound knowledge of…
\ Roles and Responsibilities DMF submissions, Annual Reports, Variations, Renewals etc. for US and Europe market. Compilation and publishing in eCTD/CTD format…
DMF API Submission experience is must Preparation of New Drug Master Files as well as DMF amendments for Brazil, US, and ROW…
Company DescriptionWe are PrimeVigilance (part of Ergomed PLC), a specialised mid size pharmacovigilance service provider established in 2008. We are proud to…
Position: Drug Regulatory Affairs Executive Industry: Pharmaceutical Manufacturing (Third Party Manufacturer) Location: Chandigarh, Baddi About Us We are a leading pharmaceutical company…
Vodafone Idea Limited is an Aditya Birla Group and Vodafone Group partnership. It is India\'s leading telecom service provider. The Company provides…
Job Req ID: 45911 Location: Ernakulam, IN Function: Other About: Vodafone Idea Limited is an Aditya Birla Group and Vodafone Group partnership.…
MEDICAL REPRESENTATIVE (ASSOCIATE) FOR A FASTEST GROWING PHARMACEUTICAL COMPANY FROM KOLKATAFOCUSING ON GASTROS,SURGEONS,GYNAE AND PHYSICIAN. Relationship Building : Build and maintain positive…
1) Responsible for obtaining approval for new pharmaceutical product 2) Updating legal or regulatory knowledge 2)Learn the regulations that apply to the…
Job Requirements • Regulatory Compliance: Ensure that company products and processes comply with relevant regulations, such as FDA (21 CFR Part 820),…
Candidate should be Msc/M.Pharm/B Pharm Experience: 4 8 years in Regulatory Dossier preparation and response Job Types: Full time, Permanent Benefits: •…
Candidate should be Msc/M.Pharm/B Pharm Experience: 0 3 years in Regulatory Dossier preparation and response Job Types: Full time, Permanent Benefits: •…
Johnson & Johnson is currently seeking an Associate Director to join our global function Data Science and Digital Health function Innovative Medicine…