A globally operating Swiss based pharmaceutical company with a reputation of delivering innovative medicines to market is currently seeking an experienced Global Program Regulatory Manager to take over projects within international regulatory affairs and regulatory compliance. This is an ideal opportunity to apply for a position where you will be involved in worldwide brands and
Great Permanent opportunity – CMC Regulatory Affairs – Consulting division.My client , global clinical research organisation is looking for a regulatory affairs associate or manager to join their team and support CMC dossier submission.Your will be working on wide variety of projects including different products which are at different stages of development. You will work
REGULATORY AFFAIRS MANAGER, AUSTRIA An interesting and self-responsible working environment is waiting for you. Within this position my client is offering extensive introduction into the position and attractive social benefits. Your tasks: * Timely preparation of high quality drug product Quality (CMC) documentation to support regulatory submmision * Function to support the definition of the technical regulatory strategy for
Une société internationale- leader dans le monde de la santé qui fournit des produits dans les domaines d’oncologie, de la nutrition clinique et de solutions de perfusion est à la recherche d’un charge (e) d’affaires réglementaires. Si vous recherchez un nouveau défi ou vous allez directement influencer la croissance de cette société sur des marches
An independent and globally operating biotechnology company that consistently delivers truly innovative and life-changing drugs is looking for an experienced regulatory affairs manager to take over projects in regulatory affairs and regulatory compliance for their Swiss affiliate based in Zurich.
Responsibilities : *Participate in project teams related with Industrial Area Projects as representative of the department and as the interface between the technical areas and the Regulatory Department *Maintain a good level of knowledge of the worldwide regulations related to marketed products, and provide informed regulatory intelligence to internal and/or external clients *Prepare and/or co-ordinate
Great Contract opportunity – 12 month contract as a Regulatory Manager – specialized in Oncology, Emerging markets, CTA, MAA – in a big pharmaceutical company , a leader in biotechnology based in UK. For more information’s please contact directly with Beata Klecz or send your cv to Beata.Klecz@secpharma.com
My client , global biotechnology company is looking for an experienced manager to take over projects in regulatory affairs and regulatory compliance.
Background: Pharmacist or Medical Doctor,Regulatory affairs experience,Regulatory affairs compliance experience ,Market access and pricing/reimbursement experience ,Drug safety reports coordination experience .
For more inforamtions please contact directly with Beata Klecz +44 207 255 6665 or send your cv to beata.klecz@secpharma.com
Freelance Contract! Regulatory Affairs Manager – South East, UK
|Freelance|6+ months |South East| Competitive
For immediate consideration call Nikolay on +44 (0) 2072556665 or e-mail nikolay.dimitrov@secpharma.com
Senior Regulatory Affairs Manager, Global Vaccines, Switzerland, Exceptional Growth Opportunities
One of the leading vaccines businesses, part of a top pharmaceutical company, is currently looking for a Senior Regulatory Affairs Manager, to join one of their main facilities located in Switzerland. As a Senior Regulatory Affairs Manager, you will join a highly skilled and multinational team of professionals.
A leading medical device company with a track record of attracting and retaining some of the brightest talent in the industry currently ( due to expansion) has two new openings for a Clinical Scien More Details
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