Regulatory Submission Planner

We have a very exciting new role and looking to hire a Regional Submission Lead (RSL) **location**: EMEA Purpose of the role The Associate Director Regional Submissions Lead will be accountable E2E for overall management and coordination of Clinical Trial submission activities across EEA countries for assigned Clinical Trials (Phase 1 - Phase 4) spanning...

We have a very exciting new role and looking to hire a **Associate Regional Submission Lead (aRSL)** Location: Belgium **Purpose of the role** The Associate Regional Submission Lead will manage the Clinical Trial Information System (CTIS) E2E for assigned CTAs in close collaboration with Translational Medicine EU Regulatory Lead to meet the strategic and...

For our site in Brussels, we are looking for a Regulatory Affairs Europe, Associate Liaison Primary Activities: - Provides administrative regulatory support during filing and review of new submissions, variations, in order to safeguard submissions according to EU requirements. - Plans and coordinates new submissions, variations, CHMP referrals, FUM. to...

In het kortbrussel / bruxelles bediende, freelancer 40 uur per week - Amandine JansenTalent Acquisition Lead Life Sciences 0032491153475 - **Regulatory Affairs Officer**: - Pharma & Sciences - Regulatory Affairs - Compile and maintain regulatory documentation databases or systems - Coordinate efforts associated with the preparation of regulatory documents...

In het kortbrussel / bruxelles bediende, freelancer 40 uur per week - Amandine JansenTalent Acquisition Lead Life Sciences 0032491153475 - **Regulatory Affairs Officer**: Pharma & Sciences - Regulatory Affairs - Compile and maintain regulatory documentation databases or systems - Coordinate efforts associated with the preparation of regulatory documents or...

The EU Regulatory Affairs Manager maintains the official record for all European product registrations, related to the design, manufacture, and sale of medical device and in-vitro diagnostic products. Also, they will update the technical files with design changes and ensure, that additional submissions are completed. The EU Regulatory Affairs Manager will be...

The RA Shared Service Delivery Model (SSDM) Regional Hub Lead is accountable for the delivery of all regulatory milestones related with strategy, planning, development, submission, registration, approval, and life cycle maintenance of Pharmaceutical Products Registration in compliance with our company standards and local applicable regulations associated...

Do you want to be part of our Oncology division, helping people fight cancer, supporting accessibility to our cancer medicines, and pursuing research in immuno-oncology to bring new hope to people with cancer? We have a new, exciting opportunity for a **Regulatory Affairs Liaison Oncology (Associate Principal Scientist) **to be based in Oss (NL), Brussels...

**Basic Functions & Responsibility**: - Has the overall responsibility for Regulatory in Belgium/Luxembourg and for managing related issues according to our ethics and standards. - Responsible for people management of Regulatory personnel in Belgium and provides clear leadership for the Regulatory group. Secures appropriate career development for the staff...

**Country Approval Specialist (Submissions) - Belgium** At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve...

Belgium Life Sciences Brussels On-site Ready to oversee regulatory compliance for diverse products?Join us as Regulatory Affairs Officer! - About The Member Company - We are a global high-tech consultancy company with a team of entrepreneurial engineers, scientists, and digital experts from around the world. Together we form a fast-growing and proud...

Working in partnership with Global Regulatory, and under the responsibility of the RA manager Personal Care FR and BNL, You will be a key point of contact to Global Regulatory and local Regulatory teams with respect to cosmetic, detergent and biocides regulation, relaying knowledge about external factors and internal impact on processes and timings. You...

**Job Description**: **Basic Functions & Responsibility**: - Has the overall responsibility for Regulatory in Belgium/Luxembourg and for managing related issues according to our ethics and standards. - Responsible for people management of Regulatory personnel in Belgium and provides clear leadership for the Regulatory group. Secures appropriate career...

**What you'll d**o** Qserve has an exciting opportunity to join our team as a Consultant Medical Devices Regulatory / US Submission Expert. As a consultant at Qserve, you serve a wide variety of clients in the medical device industry. With your regulatory knowledge of medical devices, you will be responsible for helping Qserve clients with regulatory...

**Major Functions & Responsibility**: - For assigned products ensures high quality labelling translation and artwork management. - Supports the agency interactions to ensure a seamless submission, assessment, and quick approval of the CTAs, according to the new EU CT Regulation, in cooperation with RAE Liaison, and other internal stakeholders. - For...

At Capgemini Engineering we value excellence, care, responsibility, dynamism and innovation. We offer a job with variation that leaves plenty of room for initiative and development. In fact, we are not just offering you a job, we’re inviting you to be part of our community where we will provide you trainings, tools & grounds for professional and personal...

**As a leading innovator of womens' health, we at Hologic are empowering people to live healthier lives everywhere, every day,** Our regulatory affairs team is responsible for keeping abreast of new, changing and existing regulatory requirements. They lead the development and implementation of a global vision for regulatory affairs to influence strategic...

**Description**: SASMAR is currently seeking a highly motivated and detail-oriented individual to join our team as a Regulatory Affairs Specialist. With our headquarters based in Brussels, Belgium, and operations in Sydney, Hong Kong, Mumbai, Malta, London, and Chicago, we are a fast-growing pharmaceutical company that specializes in personal care and...

**About EG** EG is the largest pharmaceutical company in Belgium. With an offering for just about every therapeutic area, we are the market leader in generic medicines and the biggest OTC company in Belgian pharmacies. We still produce many of our medicines and food supplements in Belgium. We currently have 180 employees and continue to invest in: - The...

**About EG** - EG is a Purpose driven company: at the core of everything we do, we aim to Care for People´s Health as a Trusted Partner.- EG is the largest pharmaceutical company in Belgium.- With an offering for just about every therapeutic area, we are the market leader in generic medicines and the biggest OTC company in Belgian pharmacies.- Most of our...