Experienced Regulatory Affairs Professionals

Job SummaryITech Consult AG is seeking a highly qualified Regulatory Affairs Professional to join our team in Switzerland.The ideal candidate will have substantial experience with ISO 14155, ISO 20916, and ISO 13485, as well as a strong understanding of global regulations such as 21 CFR 812, IVDR, and MDR.Key Responsibilities:Process Development and...

As a highly motivated and experienced professional, you'll thrive in our dynamic environment where no two days are ever the same. As DIRECTOR OF LOCAL REGULATORY AFFAIRS ADVANCED SYNTHESIS, you'll be responsible for ensuring the regulatory framework is aligned with global and regional strategies.Key requirements include:Exceptional communication and writing...

About the Roledsm-firmenich is a leading company in the industry, and we are seeking an experienced Regulatory Affairs Manager to join our team. As a key member of our Health, Nutrition & Care (HNC) business unit, you will be responsible for ensuring compliance with regulatory requirements across various regions.Main Responsibilities- Develop and implement...

Join our Regulatory Affairs team at Straumann Group and contribute to the development and maintenance of compliance with regulatory requirements in the medical device industry.As a Regulatory Affairs Coordinator, you will work closely with cross-functional teams to ensure compliance with regulatory requirements.Your key responsibilities will...

About the CompanySobi, Inc is a global biopharmaceutical company dedicated to providing innovative treatments for rare and debilitating diseases. We are seeking a highly skilled Regulatory Affairs Professional to join our team.Job DescriptionThe successful candidate will be responsible for ensuring compliance with current GMP & GDP regulations, quality...

**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...

Exponent is seeking a highly motivated Regulatory Affairs Manager to join our team. In this role, you will be responsible for managing complex regulatory projects, providing strategic advice and technical expertise to our clients on EU REACH and UK REACH regulations.The successful candidate will have a strong understanding of EU REACH and UK REACH...

dsm-firmenich Manager Regulatory Affairs Pharma in Kaiseraugst, SwitzerlandManager Regulatory Affairs PharmaAre you ready for the next challenge? As Manager Regulatory Affairs – Pharma within the Health, Nutrition & Care (HNC) business unit of dsm-firmenich, you will be part of a cross-functional team of around 15 employees, based in Kaiseraugst,...

About Our TeamWe are a dynamic team at Sobi, Inc. working together to bring innovative treatments to patients with rare diseases.We are seeking a Regulatory Affairs Expert to join our team, responsible for ensuring compliance with regulatory requirements and maintaining high-quality relationships with external suppliers.Key ResponsibilitiesDevelop and...

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...

We are seeking a skilled professional to lead our Regulatory Affairs function. As a Senior Regulatory Leader, you will be responsible for delivering high-quality regulatory submissions and supporting cross-functional teams in the development and implementation of global regulatory strategies.Job Expectations:Develop and execute global regulatory strategies...

About the OpportunityWe are seeking a highly skilled Global Regulatory Affairs Lead to join our team at dsm-firmenich. In this role, you will be responsible for leading the development of global API product approval strategies and managing regulatory affairs across various regions.Key Responsibilities- Develop and implement global API product approval...

**Regulatory Affairs Manager, Novartis, Basel, Switzerland** 1 unique opportunity to join Regulatory Affairs Team! Person on this position will take care of all drug regulatory affairs matters regarding the assigned indication group. Acts as an interface between global Regulatory Affairs departments and Swiss medic in order to obtain new marketing...

The Life Science Career NetworkOur client is a global pharmaceutical leader that is undergoing a cultural transformation, focusing on novel therapies in Oncology, Ophthalmology, Neuroscience, and Dermatology.This is an exciting opportunity for an experienced Senior Global Labeling Manager to join our client's team and contribute to the development and...

Job OverviewAbout UsWe are Coopers Group GmbH, a leading company in the pharmaceutical industry.Job DescriptionWe are seeking an experienced Regulatory Affairs Global Labelling Manager to join our team.The successful candidate will be responsible for maintaining regulatory compliant, competitive, and up-to-date global labeling documents. This...

Title: Manager, Regulatory Affairs (CMC)Hybrid working pattern: 2 WFHLocation: Basel or VispRelocation support is provided – subject to criteria.Today, Lonza is a global leader in life sciences operating across three continents. While we work in science, there’s no magic formula to how we do it. Our greatest scientific solution is talented people working...

My client is offering an amazing opportunity to work on site in Basel for 7 months as a Regulatory Affairs Project Manager. During your time in this role you will also have the opportunity of growth and promotion giving you the possibility of earning even more money over the period of the contract. **Requirements**: 3+ years Regulatory experience in a...

ABOUT ARCONDIS Arcondis is a global consulting company with an exclusive focus on the healthcare and life science industries, with their particularly demanding requirements on quality and regulatory aspects. We have been managing challenges and solving problems for our clients in the areas of compliance, business processes, information technology, and...

**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...

Join our global team dedicated to innovation and initiative, where physical walls and different time zones don’t limit, but encourage, collaboration. Where all contributions and new ideas are explored with an open mind and work is driven by our shared values: be courageous, be accountable, be honest, be inclusive and elevate others. Job Description...