Associate Director, Regulatory Cmc

**Site Name**: UK - London - New Oxford Street, Switzerland - Zug, UK - Hertfordshire - Stevenage **Posted Date**: Nov 25 2024 Are you interested in a highly visible regulatory affairs role that allows you to drive strategy and shape integrated regulatory development across portfolios? If so, this Regulatory Affairs CMC role could be an ideal opportunity to...

Position Summary: The Regulatory Affairs Associate Manager will report to and support the Regulatory Affairs Director/Associate Director by leading the preparation and submissions of regulatory dossiers to European and Swiss competent authorities, in line with the global regulatory plan for one or more Oncology products. Principal Responsibilities: -...

Job Description Associate Director Regulatory Strategy, Switzerland OVERVIEW: - We are looking for a Swiss regulatory expert for our Swiss affiliate in Zug to grow our regulatory team and to ensure Vertex establishes and implements best practices in accordance with national requirements in Switzerland - Support and contribute to local Swiss...

**The role can be based in Munich, Germany or Zug, Switzerland** **Position Summary**: The Associate Director Pharmacovigilance (PV) International is responsible for managing local PV processes and systems in ex-US territories (focusing on Europe), maintaining compliance with local/regional PV regulations and guidance, particularly EU Good Pharmacovigilance...

**Title: Associate Director, International Advertising and Promotion Regulatory Affairs** **Location: Zug or remote (Europe)** **Reporting: Senior Director, International Regulatory Affairs** **Description**: - The Associate Director of International Advertising and Promotion (A&P) serves as an internal expert on industry codes and guidance and...

About Bioeq Bioeq AG is a Swiss biopharmaceutical joint venture between Polpharma Biologics Group and Formycon and is based in Zug. We license, develop and commercialise a biosimilar, which is a successor product of Lucentis® (ranibizumab), a successful branded biopharmaceutical. We are a young and dynamic company, supported by an international network of...

Position Summary: The Regulatory Affairs Manager will report to and support the Regulatory Affairs Director by leading the preparation and submissions of regulatory dossiers to European and Swiss competent authorities, in line with the global regulatory plan for one or more Oncology products. Principal Responsibilities: - Provide effective regulatory and...

**Site Name**: UK - London - New Oxford Street, Home Worker - USA, Zug House **Posted Date**: Dec 3 2024 **We create a place where people can grow, be their best, be safe, and feel welcome, valued and included. We offer a competitive salary, an annual bonus based on company performance, healthcare and wellbeing programmes, pension plan membership, and...

**Reports to**:Head of MSAT **Position Summary**: As part of the MSAT team, the Associate Director of Drug Substance, Manufacturing Science and Technology (MSAT), will assume broad responsibility for tech transfer, process qualification and validation at contract drug substance manufacturing sites. The Associate Director of DS MSAT is responsible for...

**Site Name**: USA - Pennsylvania - Upper Providence, Belgium-Rixensart, GSK HQ, USA - Massachusetts - Waltham, Zug House **Posted Date**: Dec 11 2024 **Job Purpose**: The Executive Director is accountable to the SVP, Regulatory Affairs Therapeutic Group, for influencing and driving the overall direction and strategy for the Established Products (EP)...

Hobson Prior are in search for an Associate Director Clinical Operations to join a fantastic pharmaceutical company on a permanent basis with the ability to work remotely. Our client is focused on supplying patients with important medicines. Please note that to be considered for this role you must have the right to work in this location. **Key...

**Snr Director Regulatory - Contract**: In collaboration with a well funded fast paced BioTech, BioTalent are looking to connect a seasoned Regulatory Industry professional to fulfil EU and UK requirements in alignment with the Global Team. This role will offer you - 3-6 month rolling contract - Ability to work part time - Hourly pay rate - Remote...

Site Name: UK – London – New Oxford Street, Home Worker - USA, Zug HousePosted Date: Dec 3 2024About Us: We create a place where people can grow, be their best, be safe, and feel welcome, valued and included. We offer a competitive salary, an annual bonus based on company performance, healthcare and wellbeing programmes, pension plan membership, and...

**Company Description** Deciphera, a member of ONO, is a biopharmaceutical company focused on discovering, developing and commercializing important new medicines to improve the lives of people with cancer. We are leveraging our proprietary switch-control kinase inhibitor platform and deep expertise in kinase biology to develop a broad portfolio of innovative...

**Job Overview** The position of the Director Regulatory for Combination Product, Medical Devices and Emerging Technologies is based in the HQ of SHL Medical AG in Zug. It holds overall responsibility for Regulatory matters related to combination products, medical devices and emerging technologies. The holder is responsible for establishing applicable...

If you are currently performing the role for a Clinical Trial Manager or Clinical Operations Manager and looking to step into a Director position this is your chance! My Client who is an international company is looking for a Associate Director - Clinical Operations to join their team in the office in Zug, Switzerland on a 12 month contract. They are focused...

**Associate Director, International Medical Affairs Operations** Location(s): Zug, Switzerland Level of position: Associate Director Position type: office-based Reporting Line: VP Medical Affairs, International ***How will your role help us transform hope into reality?** ***This position reports into the VP of International Medical Affairs and will...

**Site Name**: UK - London - New Oxford Street, Stevenage, Switzerland - Zug, USA - Massachusetts - Waltham, USA - Pennsylvania - Upper Providence, Warsaw **Posted Date**: Nov 21 2024 MEDICAL DIRECTOR- ONCOLOGY CLINICAL DEVELOPMENT Are you looking to join an ambitious oncology clinical development organisation, focusing on the development of ADCs in the GI...

QA Associate This position will support the Global data collection automatization activities to improve CMO and suppliers data collection and KPI process establishment. The role reports into the Senior Director of External Quality and sits within a growing External Quality Operations team that is part of our expanding Global Center of Excellence focused on...

The Senior Clinical Project Manager/Associate Director, Clinical Operations will provide operational expertise within the Research and Development function to ensure timely initiation, execution and reporting of clinical trials in accordance with ICH/GCP and all applicable requirements (including local regulations) to support licensure of products in the...