Regulatory Specialist

QbD - Regulatory Affairs Specialist - ATMP in BelgiumTable of ContentsJoin our QbD team where Regulatory Affairs services cover regulatory strategy, CTD registration dossier writing, eCTD compilation, and submission to competent authorities, extending to Vigilance. We provide support from concept to commercialization. Are you passionate about ensuring...

QbD Belgium Regulatory affairs Table of Contents At QbD our RA Services go from regulatory strategy, clinical, technical file to Vigilance. We support from idea to commercialization. Do you want to support companies throughout the entire medical device regulatory lifecycle? Do you want to guide them through complex regulatory requirements? This...

RA The UK Regulatory affairs Table of Contents The UK team of the international QbD group, is a specialist regulatory and pharmacovigilance consultancy company. Our services consist in providing consultation throughout product development, regulatory approval, market launch, and into life cycle management. We have been offering support to life...

RA Austria Regulatory affairs Table of Contents QbD Austria , part of the international QbD group, is a young and growing consulting company offering services and training on regulatory affairs, regulatory compliance, business organization and quality assurance in the pharmaceutical, food supplement and medical device industry. Our headquarters...

Qarad Belgium Regulatory affairs Table of Contents Qarad, part of the QbD group, is a fast-growing consultancy company assisting manufacturers of In Vitro Diagnostics (IVD) and Medical Devices (MD) in coping with European and other regulations. Our objective is to provide manufacturers with practical solutions in the area of regulatory affairs...

Ben jij een ervaren Regulatory Affairs Specialist met een passie voor het waarborgen van naleving van regelgeving binnen de life sciences industrie? Wij zijn op zoek naar getalenteerde professionals die onze organisatie kunnen vertegenwoordigen bij bedrijven in ons Randstad netwerk in Antwerpen en Kempen.Als Regulatory Affairs Specialist in Life Sciences ben...

Ben jij een ervaren Regulatory Affairs Specialist met een passie voor het waarborgen van naleving van regelgeving binnen de life sciences industrie? Wij zijn op zoek naar getalenteerde professionals die onze organisatie kunnen vertegenwoordigen bij bedrijven in ons Randstad netwerk in Antwerpen en Kempen.Als Regulatory Affairs Specialist in Life Sciences ben...

Job Summary:Job description: The primary responsibility is to work with local evaluating competent authorities and with the European registration authorities (ECHA & EFSA) to register and gain approval of biocidal and pesticidal active substances, products and emergency authorisation permits for EU markets. The person must have strong knowledge and...

On top of the regulatory trends? A heart for sustainability? So do we Let's grow together.Main responsibilities and key tasks As part of the regulatory team, ensuring our complete product offering is compliant with the relevant legislation. As part of a multifunctional project team, provide regulatory input on new product developments. Alert the business on...

QbD The UK Quality management, Regulatory affairs Table of Contents The UK team of the international QbD group, is a specialist regulatory and pharmacovigilance consultancy company. Our services consist in providing consultation throughout product development, regulatory approval, market launch, and into life cycle management. We have been...

Qarad Belgium Regulatory affairs Table of Contents Qarad, part of the QbD group, is a fast-growing consultancy company assisting manufacturers of In Vitro Diagnostics (IVD) and Medical Devices (MD) in coping with European and other regulations. Our objective is to provide manufacturers with practical solutions in the area of regulatory affairs...

FunctieomschrijvingOns bedrijf is op zoek naar een specialist inzake Product Regulaties voor Fumiganten om ons team in Europa te versterken. De gekozen kandidaat zal verantwoordelijk zijn voor het beheer van productregistraties van biociden en pesticiden en de naleving van de regelgeving in overeenstemming met de Europese regelgeving.Functieomschrijving:- De...

We are looking for a Quality Operation Specialist to join our team and oversee the quality of all products and services that we produce at Tagaddod.Our Quality Operations Specialist responsibilities include developing quality standards, conducting tests and identifying issues in the production of our productsUltimately, you will work with a team to ensure...

ASSET MANAGEMENT - COMPLIANCE - AML - REGULATORY - UHNWI - ANTWERPStay vigilant on regulatory shifts, evaluating their repercussions on current business methodologies.Direct the execution of projects, initiatives, procedures, and measures in response to the fluid legal and sectoral environment.Execute thorough compliance assessments and effectively...

MissionIn direct report with the global head of science and innovation manager, your tasks are:To protect and support the company and its business growth and to strengthen its supply chain, ensuring best-in-class quality and service, and reduce the environmental impact of our business on the planet Prepare, under the coordination of the Group Regulatory...

QbD Belgium, The Netherlands Clinical, Qualification & Validation, Quality management, Regulatory affairs, Software validation Are you an expert within medical devices and passionate by helping companies in this area in their growth or to achieve their ISO13485 certificate? Apply now for the job of medical devices specialist at QbD Table of Contents ...

We are looking for an Operational Care Specialist to join our dynamic Sea Logistics Team. Your Role You are part of a team responsible for coordinating transport activities by executing the necessary bookings with our partners, executing the requisite data entry across all Kuehne+Nagel systems, and generating the required documentation, which is a major part...

We are looking for an Operational Care Specialist to join our dynamic Sea Logistics Team. Your Role You are part of a team responsible for coordinating transport activities by executing the necessary bookings with our partners, executing the requisite data entry across all Kuehne+Nagel systems, and generating the required documentation, which is a major part...

We are looking for an Operational Care Specialist to join our dynamic Sea Logistics Team. Your Role: You are part of a team responsible for coordinating transport activities by executing the necessary bookings with our partners, executing the requisite data entry across all Kuehne+Nagel systems, and generating the required documentation, which is a major...

JOB DESCRIPTION We are looking for a Sea Logistics Import Operational Care Specialist to join our dynamic Sea Logistics Team. Your Role Sea Logistics Import Operational Care Specialist is part of a team in the Operational Care Center responsible for coordinating transport activities by executing the necessary bookings with our partners (carriers),...