Regulatory Affairs Consultant
Enregistrez cette offre et organisez votre recherche
Créez un compte gratuit pour enregistrer des offres d'emploi, créer des alertes et revenir à cette liste depuis votre tableau de bord.
Contract
Regulatory Affairs Consultant | Medical Devices | EU MDR | Belgium | Freelance ContractAre you an experienced Regulatory Affairs professional looking for your next contract within the medical device industry. You'll have the chance to thrive in a collaborative, high-performing environment, with the opportunity to influence regulatory strategy, drive compliance, and make a real impact. If you're looking for the ability to succeed on a high-profile project with genuine scope for development, this could be the perfect next step.
In this role, you'll take ownership of regulatory submissions and compliance activities, working closely with cross-functional teams to ensure products meet EU MDR requirements and achieve successful market approvals.
Key Responsibilities
Develop regulatory strategies and submission plansPrepare and coordinate EU MDR regulatory submissionsSupport conformity assessment activitiesReview technical documentation and quality reportsApprove product labelling and marketing materialsMaintain regulatory licences, filings and change controlsWhat We're Looking ForProven Regulatory Affairs experience within medical devicesStrong knowledge of EU MDR and conformity assessmentExperience managing regulatory submissionsExcellent organisation and stakeholder management skillsFluent English (additional European languages are advantageous)Apply now Opportunities like this move quickly. If your experience matches what we're looking for, apply now and book time with me to discuss the role in more detail.
-
Freelance Regulatory Affairs Consultant — EU MDR
Il y a 6 jours
Antwerp, Flanders, Belgique Barrington James Limited Temps partielBarrington James Limited is seeking an experienced Regulatory Affairs Consultant for a freelance contract in Belgium. You will lead regulatory submissions, develop strategies, and ensure EU MDR compliance for medical devices across cross-functional teams.The role emphasizes strong submission management, conformity assessment knowledge, and stakeholder...
-
Regulatory Affairs Consultant
Il y a 6 jours
Antwerp, Flanders, Belgique Barrington James Limited Temps partielRegulatory Affairs Consultant | Medical Devices | EU MDR | Belgium | Freelance Contract Are you an experienced Regulatory Affairs professional looking for your next contract within the medical device industry. You'll have the chance to thrive in a collaborative, high-performing environment, with the opportunity to influence regulatory strategy, drive...
-
Regulatory Affairs Consultant
Il y a 3 jours
Antwerp, Flanders, Belgique Vi-Jo - Enlightened Consulting Temps pleinppExcellence Squad is a European consulting firm specializing in Operational Excellence, Quality Compliance, and Project Leadership across industries. We help organizations achieve measurable results through structured execution and performance excellence. /p pOur client, a leading medical device company based in Belgium, is looking for an experienced...
-
Regulatory Affairs Consultant
Il y a 7 jours
Antwerp, Flanders, Belgique Vi-Jo - Enlightened Consulting Temps pleinExcellence Squad is a European consulting firm specializing in Operational Excellence, Quality & Compliance, and Project Leadership across industries. We help organizations achieve measurable results through structured execution and performance excellence. Our client, a leading medical device company based in Belgium, is looking for an experienced...
-
CMC Regulatory Affairs Specialist
Il y a 4 heures
Antwerp, Flanders, Belgique USG Professionals Belgium Temps pleinOver het Bedrijf Voor onze key klant zijn we op zoek naar een Senior Regulatory Affairs Specialist. Je maakt deel uit van het Regulatory Affairs-team en bent verantwoordelijk voor de registratieactiviteiten van een toegewezen productportfolio. Je werkt nauw samen met collega's binnen Manufacturing, Quality Assurance, Supply Chain en de laboratoria in Puurs,...
-
Principal Scientist
Il y a 2 jours
Antwerp, Flanders, Belgique Johnson & Johnson Temps pleinAt Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to...
-
Regulatory Affairs Strategist – Medical Devices
Il y a 4 jours
Antwerp, Flanders, Belgique Vi-Jo - Enlightened Consulting Temps pleinA leading consulting firm in Antwerp, Belgium seeks an experienced Regulatory Affairs Consultant for an interim assignment with a prominent medical device company. The role involves developing regulatory strategies, coordinating submissions, and ensuring compliance with EU MDR. Ideal candidates have a strong track record in Regulatory Affairs, are organized,...
-
Biopharma Downstream Regulatory Consultant – Europe
Il y a 3 jours
Antwerp, Flanders, Belgique Ecolab Temps pleinpEcolab Life Sciences is seeking a Biopharma Technical Consultant to drive downstream purification optimization, resin performance, and regulatory change management across Biopharma manufacturing in Europe. You will collaborate with commercial, regulatory, RD, and field teams, travel regionally, advise on resin adoption, and help de-risk change while...
-
CMC Regulatory Affairs Specialist
Il y a 1 semaine
Antwerp, Flanders, Belgique Linkedin Temps pleinOver het Bedrijf Voor onze key klant zijn we op zoek naar een Senior Regulatory Affairs Specialist. Je maakt deel uit van het Regulatory Affairs-team en bent verantwoordelijk voor de registratieactiviteiten van een toegewezen productportfolio. Je werkt nauw samen met collega's binnen Manufacturing, Quality Assurance, Supply Chain en de laboratoria in Puurs,...
-
Medical Affairs Director
Il y a 4 heures
Antwerp, Flanders, Belgique EPM Scientific Temps pleinMedical Affairs Director (PR/607660) Flemish Region, BelgiumEPM Scientific are currently partnered with an international healthcare company focused on innovative wound care, skin health, and medical technologies. They are seeking a Medical Affairs Director to lead the global medical and clinical strategy across an expanding product portfolio and pipeline....
