Offres d'emploi Regulatory Submissions Associate près de chez vous

For our client, a leading pharmaceutical firm, we are actively looking for a. Senior Regulatory Affairs.. Proven track record in managing EU submissions for NPD projects, CE Mark documentation, and Notified..

As a Global Regulatory Affairs Associate, you will play a crucial role in ensuring compliance with.. Manage and maintain product registrations and submissions for global markets Prepare and review..

About the Role As a Senior Clinical Research Associate with TFS HealthScience, you will be a vital part.. Key Responsibilities Submission & Amendment Support. Assist with initial and ongoing submissions..

Are you a fluent German speaker with expertise in regulatory affairs? Do you have a passion for.. Key Responsibilities. Provide strategic guidance on regulatory requirements and submissions in Germany..

We help create sustainable change by stimulating innovation, unlocking data possibilities, navigating risk and regulatory complexity, optimising deals, and aligning costs with business strategy..

Your main tasks Develop and implement regulatory strategies in collaboration with regulatory sub functions and teams like quality and clinical Prepare and manage CMC regulatory submissions..

Job Description Primary Function of Position. The Senior Regulatory Affairs Specialist plays an.. and maintaining EU Medical Device dossiers, CE Mark submissions, and associated Technical Documentation..

0. Duration. 6 months with possible extension Your mission. Author review CTD module 3.2 (drug substance product) for biological products to support global regulatory submissions for the..

Your Mission. Manage all post marketing regulatory activities of chemical pharmaceutical drug products.. To author, review and lead high quality documents for regulatory submissions. Prepare response to..

Their ideas, big and small, genuinely improve the world. And that's the kind of work we want to be part of.We are looking for an Associate Director, Regulatory Affairs Small Molecules (f m d) to..

Innovative Biologic submissions. early to late phase Our client is an R&D driven biotech company based.. Your Challenges Develop and implement regulatory strategies for biologics drug development Provide..

You will be responsible for Conducting environmental exposure assessments for European regulatory submissions of plant protection productsProviding strategic scientific advice to clients on..

Die qualitativ hochstehenden Services werden verstärkt nachgefragt. Wir suchen deshalb eine n erfahrene n Sr. Regulatory Affairs Consultant für neue Projekte in der Schweiz. Tragen Sie in..

Ihre Aufgaben. Führung und Unterstützung der Mitarbeitenden RA Verantwortlich für die Regulatory Compliance der Medizinprodukte Enger Kontakt zu den externen Fachstellen (Benannte Stelle..

Join a Leading Regulatory Affairs Team!About Our ClientWith a diverse portfolio of iconic brands across.. Join the team to discover why!The OpportunityOur client is seeking an experienced Associate Regulatory..

The PositionClinical Trial Regulatory Lead The Pharma Development Regulatory (PDR) organization develops.. build regulatory submissions and deliver fit for purpose solutions to achieve organizational goals and..

Requirements.Ability to interpret regulations and guidelines.Experience and knowledge in the preparation of regulatory submissions and supportive amendments or supplementsStrong communication..

Guidelines and manuals, patient informed consents) Manage and prepare ethical and regulatory submissions in collaboration with the SAKK Regulatory Affairs Unit Ensure efficient and timely..

For his Regulatory Affairs Department, Debiopharm Research & Manufacturing in Martigny is looking for a.. To author, review and lead high quality documents for regulatory submissions. Prepare response to..