Regulatory Change Expert

Switzerland - Zürich - Process, project and program management - Global Wealth Management **Job Reference #** - 264560BR **City** - Zürich **Job Type** - Full Time **Your role** - Are you a highly motivated and capable individual? Do you enjoy working in a dynamic and diverse environment? Do you want to strive for impact in UBS Global Wealth...

We have an exclusive mandate for one of our clients in Medical Devices based in Canton of Neuchatel. As a Regulatory Affairs Manager, you will be responsible for: - Support new product development by using in-depth knowledge and understanding of US domestic and international medical device, regulations (including 510k, and International dossiers) - Lead...

Location: role can be located anywhere in Europe At Corza Medical, our mission is to support surgical providers with remarkable service, trusted performance, and outstanding value by creating an unmatched experience that stems from listening to the surgical experts themselves. Our product family is the result of years of experience championing surgeons and...

At Roche, we are committed to fostering diversity, equity, and inclusion in our global operations. Our goal is to ensure that everyone has access to the best possible healthcare solutions. To achieve this vision, we need talented individuals who share our passion for innovation and customer satisfaction.The One PDR Early Talent ProgramThis two-year program...

**EINFÜHRUNG**: As a preferred supplier for Roche in Basel, we are looking for an individual as **Technical Regulatory Support Manager**: with contract for 1 year. The earliest start date is within 2 months. Home Office will be possible for max. 2 days a week. **AUFGABENBESCHREIBUNG**: - Proactively support the technical regulatory department on the...

**Regulatory Affairs Coordinator 4881 SRS** As the Regulatory Affairs Coordinator you will support the Regulatory team in managing, tracking and archiving regulatory requests received from our partners companies in their respective territories. **Main Responsibilities**: - Ensuring all documents/declarations/statements are signed by company...

**THE POSITION**: This role of is the senior most regulatory role within EPD in the Emerging Market business unit_. _As a leader, the role of the Director, Regulatory Affairs is to combine knowledge of scientific, regulatory and business issues to support and partner the business by ensuring the successful development, manufacture and distribution of...

Contract Type: Permanent Closing date: Reference: VN1863 About Us Vectura Fertin Pharma’s ambition is to become a market-leading wellness and healthcare business. Formed in March 2022, the business brings together two unique organizations: Vectura, experts in inhalation technology and Fertin Pharma, experts in oral and intra-oral delivery systems. We...

**Takeda Neuchâtel** **Site de Production Biotech | Biotech Manufacturing Site** Takeda is an industry-leading, global pharmaceutical company with an unwavering dedication to putting patients at the center of everything we do. We live our values of Takeda-ism - Integrity, Fairness, Honesty, and Perseverance - and are united by our mission to strive...

Contract Type: Permanent Closing date: Reference: VN1710 - Who we are - Vectura Fertin Pharma’s ambition is to become a market-leading wellness and healthcare business. Formed in March 2022, the business brings together two unique organizations: Vectura, experts in inhalation technology and Fertin Pharma, experts in oral and intra-oral delivery systems. -...

**Quality Assurance & Regulatory Affairs (QA/RA) Manager - Medical Devices** ALTOGEN is a Swiss engineering and consulting company specialized in life sciences with proven expertise in pharmaceuticals, biotechnology, medical devices. With several years of experience, technical expertise and project coordination, we support our partners throughout all areas...

REGULATORY AFFAIRS Associate Director, Europe (with focus on Switzerland) Regulatory Affairs, Basel, Switzerland Reports To: Director, Team Lead of EU Regulatory Affairs **Job Description**: The (Swiss) Regulatory Affairs lead will report to the team lead of Regulatory Affairs Europe and will have dotted line reporting to the Swiss General Manager. The...

**The Role**: Reporting to the Director Quality Systems & Compliance the AD Regulatory Compliance will be responsible to be the liaison function between Quality and the Regulatory CMC functions of Moderna. The role will implement and continuously improve required processes to ensure the compliance of Moderna’s product with the registered...

**The Role**: Reporting to the Director Quality Systems & Compliance the Snr Manger/AD Regulatory Compliance will be responsible to be the liaison function between Quality and the Regulatory CMC functions of Moderna. The role will implement and continuously improve required processes to ensure the compliance of Moderna’s product with the registered...

Company Overview: BeiGene, Ltd. (NASDAQ: BGNE; HKEX: 06160) is a global, commercial-stage, research-based biotechnology company focused on molecularly targeted and immuno-oncology cancer therapeutics. With a global team of over 9,000 employees located in China, the United States, the EU, the UK, Switzerland and Australia, BeiGene is advancing a pipeline...

Takeda is an industry-leading, global pharmaceutical company with an unwavering dedication to putting patients at the center of everything we do. We live our values of Takeda-ism - Integrity, Fairness, Honesty, and Perseverance - and are united by our mission to strive towards Better Health and a Brighter Future for people worldwide through leading...

Proclinical are working alongside a pharmaceutical organisation who are recruiting for an individual to join their team. This role is on a contract basis. The opening position is for a Regulatory Affairs Manager. For more information, please get in touch now! **Responsibilities**: - Conduct regulatory evaluations for aberrations and change control. -...

The Position Clinical Trial Regulatory Lead  The Pharma Development Regulatory (PDR) organization develops and maintains the licensees that permit Roche to market and sell its life improving therapies worldwide. We are the stewards of the safety and efficacy of medicines, collaborating with regulators of every country in which Roche does business...

**At Bayer we’re visionaries, driven to solve the world’s toughest challenges and striving for a world where ,Health for all, Hunger for none’ is no longer a dream, but a real possibility. We’re doing it with energy, curiosity and sheer dedication, always learning from unique perspectives of those around us, expanding our thinking, growing our...

**_The Life Science Career Network_** **Technical Regulatory Support Manager -5446** Our client is a pioneer in Drug Discovery and Development and one of the frontrunners in Personalised Healthcare. As the world's largest R&D spender in the pharmaceutical and diagnostics domain, they work in a vast number of drug discovery & therapeutic areas and are...