Aktuelle Jobs im Zusammenhang mit Associate Regulatory Affairs Director – Join Innovative TeamNonStop Consulting - Zug - NonStop Consulting
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Manager/associate Director
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Regulatory Affairs Manager
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Zug, Schweiz Johnson & Johnson VollzeitJohnson & 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...
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Regulatory Director for Combination Product
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Zug, Schweiz SHL Medical AG Vollzeit**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...
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Associate Director, Medical Affairs, International
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Zug, Schweiz BridgeBio VollzeitBridgeBio International Zug, Switzerland Commercial **About BridgeBio**: **BridgeBio** is a biopharmaceutical company founded to discover, create, test, and deliver transformative medicines to treat patients who suffer from genetic diseases and cancers with clear genetic drivers. We bridge the gap between remarkable advancements in genetic science in...
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Interim Director Medical Affairs
vor 10 Minuten
Zug, Zug, Schweiz Hays VollzeitInterim Director Medical AffairsStart:asapWorkload:100%Duration:9-12 monthsLocation:Zug, SwitzerlandAbout the OpportunityWe are supporting our client, an international biopharmaceutical company, in the search for an experienced Interim Director Medical Affairs. In this senior role, you will act as a subject matter expert within Medical Affairs and play a...
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Global Regulatory Affairs Manager, Vaccines
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Zug, Schweiz GSK Vollzeit**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...
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European Regulatory Affairs
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Zug, Schweiz Proclinical VollzeitProclinical are recruiting a European Regulatory Affairs - CTA Liaison for a biotech corporation. This role is on a contract basis and is located in Zug. **Responsibilities**: - Collaborate with regulatory affairs consultants/service suppliers on CTA proposals. - Serve as a representative for EU regulatory affairs at cross-functional study management team...
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Emea Medical Affairs Director, Evidence Strategy
Vor 6 Tagen
Zug, Schweiz Johnson & Johnson Vollzeit**Job Function**: Medical Affairs Group **Job Sub Function**: Medical Affairs **Job Category**: People Leader **All Job Posting Locations**: Zug, Switzerland Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the...
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Regulatory Affairs Manager
vor 2 Wochen
Zug, Schweiz Proclinical VollzeitProclinical are recruiting a Regulatory Affairs Manager for a biotech corporation. This role is on a contract basis with the ability to work remotely in Europe. **Responsibilities**: - Handle the relationship with the Clinical Research Organisation contracted for some clinical studies. - You will assist with different regulatory proposals to the marketing...
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International Government Affairs Director
vor 2 Wochen
Zug, Schweiz Exact Sciences Corporation VollzeitPosition Overview The International Government Affairs Director, Switzerland is responsible for coordinating activities with external stakeholders (political, patient, and others) focused on market access for Exact Sciences products in target expansion markets around the world. Collaborating closely and cross-functionally with the Medical, Market Access,...
Associate Regulatory Affairs Director – Join Innovative TeamNonStop Consulting
Vor 3 Tagen
Join a Leading Regulatory Affairs Team About Our Client With a diverse portfolio of iconic brands across 20 countries, our client operates in Australia & New Zealand, Asia, and Africa. Their team is dedicated to putting people’s health first every day, and they pride themselves on their unique blend of leadership and empowerment. Our client, celebrated as a Best Place to Work in 2021, is a trailblazer in the health and wellness industry. Known for their innovation, motivation, and unwavering commitment to customer health, they offer a work environment that their employees love. Join the team to discover why The Opportunity Our client is seeking an experienced Associate Regulatory Affairs Director, Europe, to become an integral part of their Regulatory Affairs team. This full-time role is pivotal in steering and managing strategic and operational regulatory activities across Europe, including the EEA, Eastern Europe, Switzerland, and the UK. Key Responsibilities Lead European Regulatory Operations Oversee regulatory activities in Switzerland and coordinate those in the EEA, Eastern Europe, and the UK. Ensure compliance and support for the Middle Eastern and African markets where our client holds marketing authorizations. Develop and Maintain Procedures Implement and update regional Regulatory Affairs procedures and ensure staff training. Champion regulatory information management systems and ensure their alignment with organizational systems. Regulatory Leadership and Compliance Align regulatory affairs with business objectives, ensuring timely market introduction of new products. Interface with various key functional groups to provide quality regulatory input. Promote cross-regional regulatory collaboration and knowledge sharing. Commercial Support Develop and optimize regulatory strategies for new business opportunities in Europe. Conduct regulatory due diligence for new products and provide strategic regulatory guidance. Support major commercial expansion projects and the creation of product registration dossiers. About You To excel in this role, you should have a recognized degree in pharmacy, medicine, or a relevant science, and a minimum of 8-10 years of experience in the pharmaceutical industry, with at least 5 years in the European region. Key Requirements Thorough understanding of regulatory requirements for a range of health-related products. Familiarity with clinical, regulatory, registration, and compliance principles. Strong project planning and organizational skills, with the ability to manage multiple projects. Excellent interpersonal, communication, and influencing skills. Ability to work independently and as part of a team. Additional Requirements Occasional business travel. Commitment to the company’s values. Benefits Our client offers a supportive and dynamic work environment with a variety of benefits, including: Hybrid working arrangements. Health and wellness initiatives. Awards and recognition programs. A day off for your birthday Join a team where your expertise will make a significant impact on regulatory affairs across Europe and beyond Apply today to be part of a company that values health, innovation, and excellence. Contact me for more details and I will give you a call to discuss the role in details: email address: For a confidential discussion about this role, or to apply, then send your CV to or call me, Angelina Andreenkova, Search Specialist – Life Sciences – Switzerland, at (intern 3594). Please feel free to visit my Linked-in profile to see my references/recommendations. NonStop is one of the largest and fastest-growing specialised life sciences recruitment companies in Europe. We are proud members of the APSCo life sciences group who ensure we meet the highest quality standards within the recruitment industry. Our offices are located in the UK, Luxembourg, Switzerland, Romania, the US and the Czech Republic and we hold labour leasing licences across Switzerland.
