Emplois actuels liés à Regulatory Affairs Assistant - Leuven - PSI CRO
-
Regulatory Affairs Assistant
il y a 4 jours
Leuven, Belgique PSI CRO Temps pleinCompany Description We are the company that cares - for our staff, for our clients, for our partners and for the quality of work we do. A dynamic, global company founded in 1995, we bring together more than 1,700 driven, dedicated and passionate individuals. We work on the frontline of medical science, changing lives, and bringing new medicines to those who...
-
European Regulatory Affairs Officer
il y a 2 semaines
Leuven, Belgique Avantor Temps plein**The **Opportunity**: Avantor is currently looking for someone with a Life Sciences or Legal (Bachelor/Professional Bachelor) to join our team as a Regulatory Affairs Officer on a fixed term contract until February 2025. This is a great opportunity for someone who wants to have a broad first experience within Regulatory Affairs within the Life Sciences...
-
Regulatory Affairs Officer
il y a 5 jours
Leuven, Belgique Terumo Europe Temps pleinAt Terumo, we enhance lifesaving medical technologies for the benefit of society. Are you eager to contribute to people's health and patients' wellbeing? We'll challenge you to become a master in your field of expertise. You can invest your talents in balance with your personal aspirations - live and work in harmony. Built on our Japanese origins; we are...
-
Clinical Affairs Specialist
il y a 1 semaine
Leuven, Belgique Materialise Temps pleinBelgium (HQ) Quality The Position Materialise is a dynamic, high-tech company headquartered in Belgium, with offices worldwide. Founded in 1990, today we have over 2,300 employees around the globe. Materialise’s mission is to innovate for a better and healthier world through our software and hardware infrastructure and in-depth knowledge of additive...
-
Regulatory Compliance Specialist
il y a 1 jour
Leuven, Flandre, Belgique Terumo Europe NV Temps pleinWe require a highly experienced Regulatory Compliance Specialist to join our quality team. As a regulatory expert, you will be responsible for ensuring that our quality management system meets the latest regulatory requirements, including those set out in ISO 13485 and 21 CFR Part 820.Your expertise in regulatory affairs, combined with your knowledge of...
-
Regulatory Specialist Mea
il y a 2 semaines
Leuven, Belgique GC Europe Temps plein**GC Europe NV** is the European subsidiary of **GC Corporation**, a family-owned company with headquarters in Tokyo. It is one of the biggest suppliers of dental products with over 2300 employees all over the world and 4 production branches in Japan, the USA, China and Europe. We supply an entire range of consumer materials, equipment and facilities for...
-
Senior Medical Affairs Specialist Radiation Oncology
il y a 4 jours
Leuven, Belgique Terumo Europe Temps pleinAt Terumo, we enhance lifesaving medical technologies for the benefit of society. Are you eager to contribute to people's health and patients' wellbeing? We'll challenge you to become a master in your field of expertise. You can invest your talents in balance with your personal aspirations - live and work in harmony. Built on our Japanese origins; we are...
-
Regulatory Submissions Manager
il y a 1 semaine
Leuven, Belgique NonStop Consulting Temps pleinAre you currently working in a CRO and looking to move your career forward to Regulatory Affairs ? This is a chance to do so. We are in search of a Regulatory Submissions Manager based in Leuven, Belgium to support this quality multinational CRO's daily operations. The company is focused on hiring the most talented people and are offering a lot of support in...
-
government affairs analyst vi
il y a 1 semaine
Leuven, Flandre, Belgique TE Connectivity Temps pleinAt TE, you will unleash your potential working with people from diverse backgrounds and industries to create a safer, sustainable and more connected world. Job Overview The candidate will join TE Connectivity's Global Government Affairs Team to support the shaping of policies through strategic partnerships with government and industry groups...
-
Corporate Affairs Director Zone Europe
il y a 11 heures
Leuven, Belgique AB InBev Temps pleinSeniority Level: Director As a Corporate Affairs Director you will manage, protect and enhance AB InBev’s reputation with stakeholders; protect AB InBev’s commercial license to operate; and work towards the best possible business environment for AB InBev’s operations across the Europe Zone territory by bringing the outside in; with a strong primary...
-
Biotech Research Expert
il y a 2 semaines
Leuven, Flandre, Belgique Planet Pharma Temps pleinAbout UsWe are a recruitment agency with expertise in Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs/Writing. We have been recognised by FORBES as the 17th best professional staffing firm and won multiple awards for our commitment to excellence and service delivery.
-
Sr. QA/ra Officer
il y a 1 semaine
Leuven, Belgique Terumo Europe Temps pleinAt Terumo, we enhance lifesaving medical technologies for the benefit of society. Are you eager to contribute to people's health and patients' wellbeing? We'll challenge you to become a master in your field of expertise. You can invest your talents in balance with your personal aspirations - live and work in harmony. Built on our Japanese origins; we are...
-
Director Ra/qa Emeaa
il y a 1 semaine
Leuven, Belgique Sterigenics Temps plein***: Reporting to the VP Global QA, the Director of Quality Assurance and Regulatory Affairs - EMEAA, provides technical, compliance, and regulatory guidance to processing facilities within Europe and Asia and has responsibility for the quality oversight of Sterigenics’ quality system implementation and execution. **DUTIES AND RESPONSIBILITIES**: -...
-
Senior Biotech Researcher
il y a 2 semaines
Leuven, Flandre, Belgique Planet Pharma Temps pleinPlanet Pharma is a global staffing services company that provides specialist knowledge and close relationships with clients in the biotech industry.The client, a leading biotech company, is seeking a Research Associate to support their work on innovative research projects related to immune interventions for chronic disease treatment.The successful candidate...
-
Scientific Researcher Position
il y a 6 jours
Leuven, Flandre, Belgique Planet Pharma Temps pleinOur client, a leading biotech company, is seeking a highly skilled Research Associate to support their groundbreaking work in immune interventions for chronic diseases.The ideal candidate will have experience with cell culture and hold FELASA B or C certification.The successful candidate will perform laboratory activities to analyze the efficacy, mechanism...
-
Associate Research Fellow
il y a 2 semaines
Leuven, Flandre, Belgique Planet Pharma Temps pleinOne of our biotech clients are seeking a Research Associate to support their work The client are a biotech that work on exciting innovative research on immune interventions to treat chronic disease. In the Research Associate role, you will perform the laboratory activities to analyse the efficacy, mechanism of action and the immune responses generated by...
-
Junior Farmacie en Biomedische Wetenschappen Specialist
il y a 2 semaines
Leuven, Flandre, Belgique TalentQuest BeNeLux Temps pleinTalentQuest BeNeLux zoekt een ambitieuze Junior Life Sciences Consultant/Apotheker om ons team te verstevigen.Als Junior consultant zal je worden ingezet in verschillende domeinen, waaronder:Kwaliteit en veiligheid van productenNaleving van regelgeving voor farmaceutische productenIn Medical & Regulatory Affairs zal je werkzaamheden uitvoeren...
-
Life Sciences Consultant/Farmaceutisch Expert
il y a 2 semaines
Leuven, Flandre, Belgique TalentQuest BeNeLux Temps pleinTalentQuest BeNeLux is op zoek naar een jonge expert in de farmaceutische sector. Als Junior Life Sciences Consultant/Apotheker word je opgeleid om meer ervaren collega's te ondersteunen.Je zal worden ingezet in verschillende domeinen, waaronder:Kwaliteit en veiligheid van productenNaleving van regelgeving voor farmaceutische productenOok zal je worden...
-
Internal Sales Representative
il y a 1 semaine
Leuven, Belgique Terumo Europe Temps plein_At Terumo, we enhance lifesaving medical technologies for the benefit of society. Are you eager to contribute to people's health and patients' wellbeing? We'll challenge you to become a master in your field of expertise. You can invest your talents in balance with your personal aspirations - live and work in harmony. Built on our Japanese origins; we are...
-
Ra Officer
il y a 2 semaines
Leuven, Belgique Terumo Europe Temps pleinAt Terumo, we enhance lifesaving medical technologies for the benefit of society. Are you eager to contribute to people's health and patients' wellbeing? We'll challenge you to become a master in your field of expertise. You can invest your talents in balance with your personal aspirations - live and work in harmony. Built on our Japanese origins; we are...
Regulatory Affairs Assistant
il y a 4 semaines
Company Description
We are the company that cares - for our staff, for our clients, for our partners and for the quality of work we do. A dynamic, global company founded in 1995, we bring together more than 1,700 driven, dedicated and passionate individuals. We work on the frontline of medical science, changing lives, and bringing new medicines to those who need them.
**Job Description**:
This is a fantastic opportunity to join our international Regulatory Affairs team. You will support regulatory aspects of clinical research projects, streamline communication, maintain electronic systems and managing documents for studies in Belgium and the Netherlands.
This position will be based at our Leuven office, however there is the possibility to work up to three days a week from home.
**You will**:
- Act as a point of contact for clinical project teams and support services on regulatory matters
- Prepare draft regulatory/ethics submission dossiers
- Be responsible for document management such as filing, processing, translations and quality control
- Update and maintain (automated) tracking systems, working files, and schedules
- Organise meetings, prepare agendas and minutes
**Qualifications**:
- Ideally, you will have a College/University degree or an equivalent combination of education, training & experience
- Life Science degree is a plus
- Prior experience in an administrative role is advantageous, along with experience in, or knowledge of the Clinical Research industry
- Fully proficient in Dutch and English, and French is beneficial
The ability to plan, multitask and work in a dynamic team environment
- Excellent communication and collaboration skills
**Please submit your CV in English**
Additional Information
If you feel it is time to make your skills and knowledge visible within a growing company with true focus on its people, then PSI is the right choice for you. We have a generous benefits package here at PSI as we understand the importance of giving back to our employees. Our benefits are focused on providing you with the support to excel both at work, and in your personal life