Senior Associate Regulatory Affairs

As a Senior Regulatory Affairs Specialist, you will be responsible for ensuring compliance with regulatory requirements for biocide products. You will work closely with cross-functional teams, regulatory authorities, and external partners to facilitate the registration and approval processes for biocide products in different markets. Your expertise in...

For the expansion of our regulatory team, argenx is looking for an Associate Director/Director Regulatory Affairs, argenx, based in Europe, to support the rapid growth needed for successful commercialization. Key Accountabilities and Responsibilities: The Associate Director/Director Regulatory Affairs is a key member of the global regulatory team. This role...

**WHO ARE WE?**: At Boehringer Ingelheim we develop breakthrough therapies that improve the lives of both humans and animals. Founded in 1885 and family-owned ever since, Boehringer Ingelheim takes a long-term perspective. Now, we are powered by 53,000 employees globally who nurture a diverse, collaborative, and inclusive culture. We believe that if we have...

Location: **Gent** **#23587** **Regulatory Affairs Specialist** Vast Contract - Regio Gent **#regulatory #affairs #specialist #food** Beschik je over een masterdiploma met een voorkeur voor een specialisatie in landbouw, voeding of chemie? Heb je min. 3 jaar ervaring in Regulatory Affairs? Ben je zelfstandig, zeer communicatief en computervaardig? Lees...

As a Junior Regulatory Affairs Specialist, you will be responsible for assisting in the management of regulatory affairs activities related to our biocide products. You will collaborate closely with the regulatory affairs team and other cross-functional departments to ensure compliance with relevant regulations and standards. **Responsibilities**: - Assist...

Requisition ID - 39 - Job Family 1- Regulatory & PSRM - Country 1- Belgium - Location 1- Hybrid - About us - **Cooper Consumer Health** is a leading European consumer healthcare player that develops, produces, and distributes a diverse range of OTC (over-the-counter) products with strong brands such as Valdispert, Oenobiol, Excilor, Vitascorbol, Lashyle and...

**About us** As a leading contract development and manufacturing organization (CDMO) within the pharmaceutical industry, **Ardena** is dedicated to supporting pharmaceutical companies, from virtual biotech to major players, in bringing their valuable molecules to the clinic and market. Our commitment extends to providing a comprehensive and integrated...

For the expansion of our EMEA team, argenx is looking for a Head of Regulatory Affairs, EMEA. argenx argenx is a fast-growing global immunology company committed to improving the lives of people suffering from severe autoimmune diseases. Thanks to colleagues based in Europe, the United States and Japan, we translate immunology breakthroughs into a...

For the expansion of our EMEA team, argenx is looking for a Head of Regulatory Affairs, EMEA. PURPOSE OF THE ROLE The Head of Regulatory Affairs, EMEA, is a key member of the global regulatory team as well as the EMEA Leadership Team (ELT). This role serves as a close business partner and facilitator of regulatory activities, and is expected to contribute...

**The job**: We are looking for a Regulatory Affairs Specialist to support the global product stewardship and regulatory affairs Crop Protection team. In close collaboration with business, technology and product management, you give support in protecting the existing portfolio of products and actively engage in projects to extend our growth worldwide. This...

Key Accountabilities and Responsibilities: Leads the CMC Regulatory Affairs function within post-marketing CMC. Provides strategic leadership to support development and execution of regulatory strategies for marketed products in the US, EU, Japan and roll-out to other territories world-wide. Critical to this role are strong CMC regulatory strategy and...

Roles and Responsibilities: - Identify and permanently monitor the information needs of the internal stakeholders. - Participate in the external environment parsing, extracting relevant information. - Analyze and interpret changes to the regulatory landscape. - Keep up to date with latest guidelines from Health Authorities e.g.: EMA, MHRA, FDA, PMDA and...

We are currently looking for an experienced research associate or associate scientist to join our dynamic R&D team at argenx, where we strive to innovate and deliver groundbreaking medicines to patients. We are seeking a dedicated and mature researcher who thrives in a fast-paced, collaborative environment. In this lab-focused role, you will plan, execute...

We are currently looking for (Senior) Research Associate, with working experience in the laboratory to join our R&D team in our facility in Gent/Zwijnaarde. Work description **Responsibilities**: - Discover, characterize and optimize therapeutic antibodies - Plan and execute experiments independently including interpretation and reporting of the results -...

Gent Legal, Regulatory & Public Affairs Eneco Solar 3 - 5 jaar, 4 - 6 jaar Waar ga je werken?Eneco Belgium levert elektriciteit uit 100% hernieuwbare bronnen. Wat ons drijft? Een grote maatschappelijke betrokkenheid en verantwoordelijkheid. We willen een inspiratiebron zijn voor anderen door te laten zien dat een snelle transitie van fossiele naar duurzame...

To bolster our bioanalytical team, we're seeking a Senior Research Associate with a background in bioanalytical laboratory work. This position is based in Zwijnaarde (Ghent) and daily onsite working is required. Work description Your responsibilities include: - Contributing to the development of bioanalytical assays (ELISA, MSD, Gyros platforms) for...

Johnson & Johnson (J&J) is op zoek naar een Senior QA Associate aan voor het CAR-T-hub in Europa. De functie zal gevestigd zijn in Gent, België. CAR-T (chimeric antigen receptor T-cell therapy) is een innovatieve aanpak om kankercellen te elimineren, waarbij gebruik wordt gemaakt van de kracht van het eigen immuunsysteem van de patiënt. Ze worden...

For the expansion of our Business Information Systems (BIS) team, argenx is looking for an EMEA (Europe, Middle East and Africa) Commercial and Medical Affairs Operations Lead. The Lead will be a key member of the BIS Commercial and Medical affairs team and will act as the Digital, Process and Technology business partner for the EMEA Commercial and Medical...

The Head of CMC (Chemistry, Manufacturing, and Controls) Regulatory Affairs will lead and manage a team responsible for all aspects of CMC regulatory strategy, planning, and execution across the product lifecycle, including both development and commercial phases. This role plays a critical part in ensuring compliance with global regulatory requirements while...

We are currently looking for an (associate) technical scientist or senior research associate with demonstrated working experience in antibody discovery via phage display to join our dynamic R&D team at argenx, where we strive to innovate and deliver groundbreaking medicines to patients. Location: This position is located in Zwijnaarde (Ghent) and requires...