2 meilleures offres (regulatory affairs specialist, gent, vlg) (à pourvoir)

Senior Regulatory Affairs Specialist (Biocides)
Elements Advisory —Gand
- Doctorat
- Master
- Gestion de projet
Quality Specialist (Distribution Center)
Abbott Laboratories —Machelen
- Temps plein
- Anglais
- Microsoft Office
- Bachelier
il y a 8 jours

Other jobs to consider

Find your next job by exploring related positions.

Regulatory Affairs Senior Manager Benelux
Perrigo —Gand
Oversees the preparation, submission, approval, maintenance, and lifecycle management of regulatory dossiers, permits, licenses, certificates, authorizations,…
il y a 5 jours
REGULATORY AFFAIRS INTERNS - OBELIS SCHOOL OCTOBER 2026
Obelis Group —Bruxelles
18 days off (to be granted after start-up period: 3 months). Hybrid setting (to be granted after start-up period: 3 months). Follow-up on tasks assigned to you;
il y a 8 jours

Je souhaite recevoir la dernière alerte Emploi pour les postes de ce type : regulatory affairs specialist (gent, vlg)

En vous connectant à votre compte, vous acceptez les Conditions d'utilisation de SimplyHired et consentez à notre Politique relative aux cookies et Politique de confidentialité.

Afficher des offres d'emploi dans d'autres lieux

regulatory affairs specialist jobs near gent, vlg

Quality Assurance Tester, Bruxelles : emplois

Application Specialist, Ghent : emplois

Quality Specialist, Louvain : emplois

Senior Regulatory Affairs Specialist (Biocides)

Elements Advisory
Gand

Soumettre votre candidature

Détails de l'emploi

Qualifications

Doctorat
Master
Gestion de projet
Compétences en communication

Description complète du poste

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 biocide regulations and your ability to navigate complex regulatory landscapes will be critical to our success.

Responsibilities

Conduct regulatory assessments to determine compliance requirements for biocide products in various regions.

Prepare and submit dossiers, applications, and technical documents for product registrations and approvals.
Collaborate with internal teams to collect and compile data required for regulatory submissions.
Stay updated with the latest regulatory developments and communicate relevant changes to the organization.
Interact with regulatory authorities and external partners to address queries, resolve issues, and facilitate the regulatory review process.
Ensure compliance with labeling, packaging, and documentation requirements.
Conduct human health and environmental risk assessment.

Qualifications

Master's degree or PhD in a relevant scientific discipline (e.g., Chemistry, Biology, Toxicology) or a related field.

Strong knowledge of biocide regulations, including relevant legislation, guidelines, and registration processes.
Experience in preparing and submitting regulatory dossiers and applications for biocides or similar regulated products.
Excellent understanding of toxicology, ecotoxicology, and risk assessment principles.
Ability to interpret and apply complex regulatory requirements and communicate them effectively to non-regulatory stakeholders.
Detail-oriented with excellent organizational, analytical, and problem-solving skills.
Strong interpersonal and communication skills, with the ability to collaborate effectively with diverse teams and external partners.
Experience in project management and multitasking, with the ability to prioritize and meet deadlines.

What we offer

Pleasant working environment: We prioritize creating a positive and inclusive workplace where employees feel valued, respected, and supported. We encourage open communication, collaboration, and teamwork.

Flexible working conditions: We understand the importance of work-life balance and offer flexible working arrangements that promote productivity and well-being. We believe in empowering our employees to manage their time effectively.
Professional development opportunities: We are committed to the growth and development of our employees. We provide training programs, workshops, and opportunities to attend industry conferences, allowing you to enhance your skills and knowledge in regulatory affairs.
Cutting-edge projects: As a regulatory affairs specialist in the biocides industry, you will be involved in exciting projects at the forefront of innovation. You will have the chance to contribute to the development of sustainable and environmentally friendly solutions that make a difference.
International exposure: Our company operates in various markets in the EU. Working with us will allow you to collaborate with companies and regulatory authorities from different regions.
Competitive compensation package: We offer a competitive salary and benefits package that recognizes your skills, experience, and contributions to our company's success.
The opportunity to help build Elements Advisory.
Regular team activities during and after work.

How to apply

If you are a highly motivated and detail-oriented professional looking to contribute to the regulatory compliance of biocides, please submit your resume and a cover letter outlining your relevant experience and qualifications to [email protected]. We look forward to reviewing your application and potentially welcoming you to our team!

Soumettre votre candidature

Affinez votre recherche

regulatory affairs specialist emplois - gent, vlg

Senior Regulatory Affairs Specialist (Biocides)

Quality Specialist (Distribution Center)

Other jobs to consider

Je souhaite recevoir la dernière alerte Emploi pour les postes de ce type : regulatory affairs specialist (gent, vlg)

Afficher des offres d'emploi dans d'autres lieux

Responsibilities

Qualifications

What we offer

How to apply

Outils pour les chercheurs d'emploi

Outils Employeurs

Parcourir

Garder le contact