Regulatory Affairs Manager

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...

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 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...

The Regulatory Affairs team is expanding and is currently looking for a Regulatory Liaison. Purpose of the position: Assists in global regulatory activities and manages the operational aspects of regulatory filings, and other to health authorities. Supports global regulatory leader(s) in execution of project strategies. Key...

**Functie**: Key Responsibilities - Support admin tasks (enquiries, requests, appointments, calls, diaries) in an optimal, timely & proactive way - Ensure correct and timely onboarding of new colleagues - Management and optimisation of HR activities and processes - Lead (internal) projects like website and social media updates - Organisation of events...

**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...

Do you want to be an expert in **medical affairs** - **market access** and **regulatory affairs**? We have a great opportunity to be able to learn and to get an expert in these fields. The great thing about it, is that this mix of RA and Medical affairs or Market access is not that common in the field. This could be the reason why you as an RA professional...

For the expansion of our Clinical team, argenx is looking for a Clinical Scientist who directs the planning and implementation of clinical programs to meet corporate and clinical research goals. He/she will be the primary clinical/scientific contact for one or multiple clinical studies and provides clinical research expertise within the cross-functional...

This role supports EQ SQ Site point of contact activities for the Gent CAR-T Site and will act as first point of contact for assigned Business unit(s). In this role the individual will manage day to day support for supplier related activities within the EQ SQ scope of responsibilities for assigned Business Unit(s), including but not limited to managing...

The EMEA Associate Medical Director Neurology is a medical and scientific expert on argenx’s scientific data, products and trials, and will support and oversee execution of the EMEA Medical Affairs plans for Neurology indications, in very close collaboration with EMEA country medical affairs teams to ensure excellence in execution of medical affairs...

LEAD QUALITY TRAINING - Biotech- GhentWHAT IS OFFERED We offer strong compensation packages that reward your abilities, hard work and ingenuity in achieving success. We reward you with competitive wages and offer a strong package with additional legal benefits such as meal vouchers, eco vouchers, high health insurance (DKV) and group insurance. Depending...

At Nuwhï, we collaborate with leading organizations in the healthcare industry to provide tailored recruitment solutions. With a focus on innovation and excellence, we support companies in their mission to deliver high-quality healthcare solutions. **Company summary**: A consulting company specializing in supporting pharmaceutical companies in Regulatory...

VIB is an entrepreneurial non-profit research institute, with a clear focus on ground-breaking strategic basic research in life sciences and operates in close partnership with the five universities in Flanders. VIB is in search for a **leader** for its **Science Policy team**, reporting to the Managing Director. **Role purpose**: Lead the Science Policy...

Voor een toonaangevend consultancy bedrijf, dat bekend staat om zijn kwaliteit en betrouwbaarheid zijn we op zoek naar consultants die zich willen verdiepen in verschillende expertisedomeinen. Vanuit doorgedreven klantgerichtheid verstrekt het team professionele en gespecialiseerde adviezen en services voor de farmaceutische industrie zowel nationaal als...

The Senior Manager of Content Management will assist in the content creation efforts for the Global Medical Information function which will ensure timely and accurate responses are provided to unsolicited medical and clinical inquiries from healthcare professionals, patients, clinical sites and other healthcare organizations. This position will report to...

For the expansion of the bioanalytical team, argenx is looking for a (Associate) Director Bioanalytics, with profound experience in late-stage drug development of large molecules. The level and title will depend on the experience of the incumbent. He/she will conduct and lead bioanalytical support in all aspects for one of the argenx indication franchises....

**Introductie**: Heb je een passie voor chemie? En sta je graag in contact met verschillende partijen? Dan heeft SD Worx Jobs de vacature voor jou! **Wie zoeken we?**: De ideale kandidaat ziet er als volgt uit: - Je bezit een master diploma in een chemisch of aanverwante richting - Ervaring is niet vereist, doch een eerdere ervaring is een pluspunt - Je...

Proclinical is recruiting a Clinical Project Manager/Clinical Trial Manager for a Mid-size CRO. This role is on a permanent basis and is located in Belgium. **Responsibilities**: - Contribute to the strategy or plan for clinical development. - In the allocated clinical study, proactively identify and address problems to the head of trial operations, and/or...

**Program Manager Translational Research**: - Employer- VIB- Location- Ghent- Closing date- 18 Apr 2024- Discipline Life Science Job Type Principal Investigator Employment - Hours Full time Duration Permanent Qualification Professional certification Sector Academia- You need to sign in or create an account to a job. - Job Details - Company **Job...

**Program Manager Translational Research**: - Employer- VIB- Location- Ghent- Closing date- 19 May 2024- You need to sign in or create an account to a job. - Job Details - Company **Job Details**: - Description VIB is hiring a Program manager Translational research to lead the Grand Challenges program. The Grand Challenges Program is a translational...