Regulatory Project Manager

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...

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...

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: -...

**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...

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...

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...

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...

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...

**What it's about** In order to complement our growing Compliance team in globally, we are seeking a Project Manager who has a passion for impact, and therefore understands the importance of being hands-on to achieving success. Key responsibilities would be the following: - Manage projects of strategic importance to the Compliance team and lead those...

**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...

**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...

FULL TIME- Remote - Europa - With Professional Experience - 8/28/24**What you will be doing**: - Lead MES implementation across two sites, ensuring timely delivery, budget adherence, and compliance with quality standards. Coordinate cross-functional teams and maintain detailed project plans. - Oversee the deployment, configuration, and integration of the...

Scenic Group is a leading luxury global travel company with offices around the world and has grown over its 35+year history to include award-winning, all-inclusive escorted tours; two award - winning river cruise lines - Scenic and Emerald Waterways; and, in 2019, the World’s First Discovery Yacht - Scenic Eclipse. We are currently recruiting for the role...

**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...

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...

**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...

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...

**Responsibilities**: - Coordinate with clients, internal resources, user and stakeholders for the execution of projects - Ensure that all projects are delivered on time, within scope and budget - Develop project scopes and objective - Develop detailed project plan to track progress - Report and escalate to management as needed - Manage the relationship...

**Responsibilities**: - Coordinate with clients, internal resources, user and stakeholders for the execution of projects - Ensure that all projects are delivered on time, within scope and budget - Develop project scopes and objective - Develop detailed project plan to track progress - Report and escalate to management as needed - Manage the relationship...

**What does Thomson Reuters Labs do?** We experiment, we build, we deliver. We support the organization and our customers through applied research and development of new products and technologies. TR Labs innovates collaboratively across our core segments in Legal, Tax & Accounting, Government, and Reuters News. We undertake a diverse portfolio of projects...