epm scientific

EPM Scientific is seeking a QA-CSV Specialist & Checklyst Manager Site Key User for a Belgium-based on-site role at a leading pharmaceutical manufacturing site. The position blends CSV quality oversight with governance of a site-wide digital checklist platform.You will ensure data integrity, manage validation activities, and act as the Site Key User for...

EPM Scientific in Belgium is seeking a Quality Assurance Officer to support and maintain the Quality Management System within a regulated medical device environment. The role focuses on CAPA handling, document control, audits, and continuous improvement across multiple quality processes.You will work in a hybrid setup (2 days on-site, 3 days remote) and...

EPM Scientific in Belgium seeks a Regulatory Affairs Specialist to support market access, product lifecycle management, and compliance across EMEA. You will collaborate with Regulatory Affairs, Quality Assurance and Compliance teams, manufacturers, distributors and regulatory authorities to ensure devices remain compliant and available across assigned...

EPM Scientific is seeking an experienced Quality Assurance professional to lead global serialization quality and support a Manufacturing Digital Connect integration in Beerse. The role oversees QA governance across cross-functional teams, ensuring alignment with evolving regulatory requirements and quality standards.The position focuses on developing a...

EPM Scientific is seeking an Ocean Freight Sales Exec (Field Sales) to drive new business growth across the Benelux region. The role is based in Antwerp with 1-2 days on-site per week and requires regular travel across Belgium and the Benelux region.The successful candidate will have 5+ years of sales experience in freight forwarding or logistics, fluency in...

EPM Scientific supporting a key client on their search for an Ocean Freight Sales Exec (Field Sales). Our client is seeking an experienced Outside Sales Executive to drive new business growth across the Benelux region. Working closely with internal sales and operations teams, you will be responsible for identifying and securing new customers, developing...

Who we are ? We are Pierre Fabre Laboratories, a global leader combining pharmaceutical expertise with dermo-cosmetics to support consumers and patients at every stage of their care journey. Our portfolio includes several medical franchises and international brands such as Eau Thermale Avène, Ducray, A-Derma, Klorane, René Furterer, and Pierre Fabre Oral...

Location: Belgium (On-Site)Contract End Date: 31 December 2026 / 2027 ( there is one role ending 2026 and one ending 2027)Function: Quality / ValidationIndustry: Pharmaceutical Manufacturing About the Role QA-CSV Specialist & Checklyst Manager Site Key User Location: Belgium (On-Site)Contract End Date: 31 December 2026 / 2027 ( there is one role ending 2026...

Working Pattern: 40 hours per week | Hybrid (2 days on-site, 3 days remote)OverviewA leading medical device organisation is seeking a Quality Assurance Officer to support and maintain its Quality Management System while ensuring compliance with applicable regulatory and quality requirements.This position offers the opportunity to work within a highly...

We are seeking an experienced Quality Assurance professional to join two strategic global initiatives within a pharmaceutical manufacturing environment. Acting as the Quality representative, you will provide leadership, governance, and compliance oversight across global cross-functional teams, ensuring alignment with evolving regulatory requirements and...

Regulatory Affairs Specialist - Medical DevicesIndustry: Medical Devices / Medical Equipment ManufacturingAbout the RoleAn established international medical device organisation is seeking a Regulatory Affairs Specialist to support regulatory market access, product lifecycle management, and compliance activities across multiple EMEA markets.Working within a...

Regulatory Affairs Specialist - Medical Devices Location: Belgium (Hybrid) Industry: Medical Devices / Medical Equipment Manufacturing About the Role An established international medical device organisation is seeking a Regulatory Affairs Specialist to support regulatory market access, product lifecycle management, and compliance activities across...

At Capgemini Invent, we believe difference drives change. As inventive transformation consultants, we blend our strategic, creative and scientific capabilities, collaborating closely with clients to deliver cutting-edge solutions. Join us to drive transformation tailored to our client's challenges of today and tomorrow. Informed and validated by science...