This is where you save and sustain lives At Baxter, we are deeply connected by our mission. No matter your role at…
\ Description JOB SUMMARY Primary point of contact for clinical trial related regulatory affairs in India. Accountable for and provides management support…
Site Name: India Maharashtra Worli Mumbai Posted Date: May 11 2023 This role reports to the EVP Legal & General Counsel and…
Job Description Manager Regulatory Affairs NEW PRODUCT REGISTRATION Supports and ensures submission of new drug approvals for assigned therapeutic area in India…
Department Details Role Summary Effectively support the Clinical strategy from TPP till submission of the dossier to regulatories like (FDA, EMEA, DCGI,...)…
\ Who are we? Teva is a global pharmaceutical leader and the world\\\'s largest generic medicines producer, committed to improving health and…
Who are we? Teva is a global pharmaceutical leader and the world\'s largest generic medicines producer, committed to improving health and increasing…
Job Description Associate Director – Regulatory Affairs Our Regulatory Affairs team bring new medical advancements to the world by facilitating communications and…
\ Description JOB SUMMARY Primary point of contact for clinical trial related regulatory affairs in India. Accountable for and provides management support…
Location: Delhi NCR (Delhi/ Gurgaon)\ Experience: 1\\xe2\\x80\\x932 year Experience in Medical devices (Fresher with interest in Medical devices may also apply)\ Qualifications:…
\ Company Description\ We are the company that cares \\xe2\\x80\\x93 for our staff, for our clients, for our partners and for the…
\ Job Description:\ \ Handling of filter validation activities including review of PPQ form, filterability trial documents, filter validation protocol and report.…
\ \ \ \ \ \ From 12 to 15 year(s) of experience\ \ \ 9 30,00,000 40,00,000 P.A.\ \ \ \…
Job Description Designation: HEAD QUALITY ASSURANCE Location: Dehradun Reporting To: Manufacturing Head Industry: Medical Device KEY RESPONSIBILITIES: Incumbent will be overall responsible…
\ \ The Manager QA/AC plays a critical role in the development and launch of new pharmaceutical products within the organization. This…
\ Job Description : The incumbent will be responsible for reviewing and finalizing regulatory documents, providing regulatory documents to institutional and ecommerce…
\ \ \ \ \ Title: Sr Exe Rnd (Form Dev) \ \ \ \ \ \ \ \ \ Date: Feb…
\ \ Be a part of a global pharmaceutical firm. \ Opportunity to work with one of the fastest growing organization in…
\ Site Name: India Maharashtra Worli Mumbai Posted Date: Jun 28 2023 1. Compilation and submission of Quality Regulatory Dossiers for following…
\ Literature search and study designing of Bioavailability and Bioequivalence studies of oral & non oral products(injectable, Semisolids, TDS etc.) towards different…