Job Req ID: 45911 Location: Ernakulam, IN Function: Other About: Vodafone Idea Limited is an Aditya Birla Group and Vodafone Group partnership.…
About the internshipPosition Summary:As a Regulatory & Compliance Intern, you will be supporting the Regulatory & Compliance team in ensuring that Soulflower\\\'s…
Vodafone Idea Limited is an Aditya Birla Group and Vodafone Group partnership. It is India\'s leading telecom service provider. The Company provides…
Job Title Manager Regulatory AffairsIndustry PharmaWork location NoidaExperience required 8+ yearspackage upto 10LPAJob Description:Manager Regulatory Affairs having experience of at least 4…
Department: RA Semaglutide and GLP 1, Global Regulatory AffairsAre you passionate about ensuring regulatory compliance for patient focused products and/or managing product…
Johnson & Johnson is currently seeking an Associate Director to join our global function Data Science and Digital Health function Innovative Medicine…
MEDICAL REPRESENTATIVE (ASSOCIATE) FOR A FASTEST GROWING PHARMACEUTICAL COMPANY FROM KOLKATAFOCUSING ON GASTROS,SURGEONS,GYNAE AND PHYSICIAN. Relationship Building : Build and maintain positive…
Position Title: SE / AM (Regulatory) Department: Regulatory Location: Mumbai Position Summary: The SE / AM (Regulatory) is responsible for monitoring all…
We are seeking a meticulous and dedicated Regulatory Affairs and Quality professional to ensure our pharmaceutical products meet regulatory and quality standards.…
Company Description At Intuitive, we are united behind our mission: we believe that minimally invasive care is life enhancing care. Through ingenuity…
Candidate should be Msc/M.Pharm/B Pharm Experience: 4 8 years in Regulatory Dossier preparation and response Job Types: Full time, Permanent Benefits: •…
Company DescriptionDr. Reddys Laboratories Ltd. is a leading multinational pharmaceutical company based across global locations. Each of our 24,000 plus employees comes…
JOB DESCRIPTION You are a strategic thinker passionate about driving solutions in Regulatory Reporting . You have found the right team. As…
Job Requirements • Regulatory Compliance: Ensure that company products and processes comply with relevant regulations, such as FDA (21 CFR Part 820),…
Job description:Roles and Responsibilities: Ensure timely authoring and submission of dossiers (Module 2 5) for regulated and ROW in the eCTD format…
Company DescriptionWe are PrimeVigilance (part of Ergomed PLC), a specialised mid size pharmacovigilance service provider established in 2008. We are proud to…
DMF API Submission experience is must Preparation of New Drug Master Files as well as DMF amendments for Brazil, US, and ROW…
Summary of the Position:The Product Support Engineering team is responsible for sustaining activities that support products in the field. This team is…
Assist in the preparation and review of regulatory dossiers in CTD/eCTD format for submission. Support in the compilation of documentation for New…
As an R&D Scientist in the API Development team, you will be responsible for independently planning and executing the synthesis of drug…