Manager 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: Principal Responsibilities: - Provide effective strategic and tactical leadership to support global regulatory plans including: - Conducting regulatory review of documents for health authority submissions - Representing the regulatory function on cross-functional teams and communicate regulatory requirements to ensure optimal execution of...

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...

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: -...

BioTalent are partnered with an exciting company to assist their search for a newly created Regulatory Affairs Project Manager on a permanent basis as part of their ongoing growth plans. **Key Responsibilities**: Maintain the approved dossiers of the lifecycle of the products Ensure that Regulatory procedures and records with respect to CMC / Quality are...

**The R&D Procurement Research Category **is recruiting for **a Manager, Research Procurement, CMC, **preferably located in **Beerse (Belgium) or Springhouse/Titusville (US). Secondary locations are Leiden (The Netherlands), Schaffhausen/Zug (Switzerland), Tampa/Raritan/New Brunswick (US), Prague (Czech Republic) and Shanghai (China).** The** Manager,...

For more than 130 years, diversity, equity & inclusion (DEI) have been part of our cultural fabric at Johnson & Johnson and woven into how we do business every day. Our commitment to respect the dignity and diversity of all is embedded in our Credo. We know that the success of our business depends on having the best talent in a workforce that reflects the...

Johnson & Johnson is currently seeking a Regulatory Affairs Manager to join our local Regulatory Affairs team located in Zug, Switzerland. This role will be working in a hybrid working model. We are looking for a highly motivated individual to join our team as a Regulatory Affairs Manager. In this position, you will play a crucial role in ensuring adherence...

**Job Description Summary** Reporting to the SVP and Head of International, based in Zug, and the VP Regulatory Affairs & Quality, based in San Diego, this professional will be part of both the International Leadership and the Global Regulatory Affairs Teams with responsibility for oversight of EU and International Regulatory activities to support corporate...

Janssen Supply Group is recruiting a Pharmaceutical Regulatory Compliance Manager within the Johnson & Johnson Regulatory Compliance (JJRC) team! The position will be preferably located in Latina, Italy, Zug, Switzerland, Horsham, PA, Malvern, PA, Titusville, NJ, Raritan, NJ, Beerse, Belgium, Leiden, Netherlands or Cork, Ireland. The Pharmaceutical...

Seagen is a global, multi-product biotechnology company dedicated to developing and commercializing transformative cancer medicines. As the industry leader in antibody-drug conjugate (ADC) technology, we pioneered a new generation in the science of harnessing antibodies to deliver cell-killing agents directly to cancer cells. Seagen’s dedication to...

Proclinical are recruiting a Regulatory Project Manager for a pharmaceutical organisation. This role is on a contract basis and is located in Zug. *** **Responsibilities**: - Handle regulatory duties affiliated with the development, assistance, and deployment of the company's non-medical and medical device software products. - Supervise and examine both...

In this role you will manage activities associated with regulatory approval of** in vitro diagnostic medical device**s. You will be responsible for activities which lead to and maintain domestic and international regulatory approval to market devices. Additionally, you are responsible for assessment of device changes for regulatory...

Proclinical are recruiting a Regulatory Affairs Manager (LSW) - RZ for a pharmaceutical establishment. This role is on a contract basis and is located in Zug with hybrid working available. The client is focused on supplying novel solutions for various illnesses. **Responsibilities**: - Accountable for upkeep of product technical files and for current...

**Site Name**: Belgium-Wavre, Italy - Siena, Switzerland - Zug, UK - London - New Oxford Street, USA - Maryland - Rockville, Warsaw Rzymowskiego 53 **Posted Date**: Oct 31 2024 **Global Regulatory Affairs Manager, Vaccines Therapeutic Group**: Job purpose: As a **Global Regulatory Affairs (GRA) Manager**, you will join the GRA Vaccines Therapeutic Group in...

**Regulatory Affairs Manager (M/F/d)**: - Location Zug - Contract type temporary contract - Start/End: ASAP - 12 months after start date Tasks & Responsibilities - Manages regulatory responsibilities associated with the development, support, and deployment of the Company’s non-medical and medical device software products. - Manages development and...

**ROLE OVERVIEW** **WHAT YOU CAN EXPECT TO DO IN THE ROLE**: Reporting to the EVP, Regulatory & Scientific Affairs, you will partner with the Head of Regulatory Countries and Head of Commercial EU & International to ensure that regulatory licenses are submitted to grow the business. You liaise, negotiate, and orchestrate meetings and teleconferences with...

**Abbott** **is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 115,000 colleagues serve people in more than 160...

Meda Pharmaceuticals Switzerland GmbH At VIATRIS, we see healthcare not as it is but as it should be. We act courageously and are uniquely positioned to be a source of stability in a world of evolving healthcare needs. Viatris empowers people worldwide to live healthier at every stage of life. We do so via: Access - Providing high quality trusted...