20 English-speaking jobs in Geel

We are constantly exploring. And have been since 1952. Driven by our passion for nuclear technology and empowered by our unique infrastructure. SCK CEN explores the limits of the possible. In this way, we continuously expand our knowledge in various nuclear fields.

Principal Scientist, CMC Regulatory Affairs - Combination Products provides regulatory subject matter expertise for drug-device combination products. This role develops and executes regulatory strategies for submissions and lifecycle management globally.

MSAT Process Engineer supports commercial manufacturing through process/method optimization and technology transfer. Focus is on cell culture or purification at lab/manufacturing scale, requiring strong scientific knowledge and GMP understanding.

Project Planner develops and maintains detailed project schedules for construction and infrastructure projects. This role monitors progress, analyzes performance, and prepares reports to support decision-making. Strong planning, analytical, and project control skills are required.

Junior QA Associate provides Quality Assurance oversight for Mobile Equipment Cleaning and acts as the primary Quality Point of Contact. The role ensures cGMP compliance while supporting operational departments and contributing to quality systems.

Experienced Senior Planner needed for a major pharmaceutical project. Responsibilities include developing detailed schedules, managing EVM, and reporting progress across the project lifecycle. Requires 5+ years in pharma/life sciences and P6 proficiency.

Senior or Principal Scientist to manage and coordinate metabolite profiling and identification studies for drug discovery and development programs. Responsibilities include designing, planning, and conducting in vitro incubations, performing LC/MS analysis, and serving as a subject matter expert for biotransformations. PhD in a relevant field and hands-on experience in structure elucidation using mass spectrometry are required.

Experienced Database Engineer needed to develop and maintain mission-critical data solutions. Responsibilities include designing relational databases, optimizing PL/SQL, and building reports with JasperReports. Requires 5+ years in PL/SQL and 3+ years with JasperReports.

Leads late-phase clinical development (P2b/3) of neuropsychiatry compounds. Develops and executes clinical development plans, designs trials, and prepares regulatory filings. Manages a matrix-based clinical team and oversees safety and medical activities. Requires an MD with post-doctoral training and 7+ years of clinical research experience, including 3+ years in phase II/III development.

Supervise mechanical installation teams for process equipment in pharmaceutical construction. Ensure compliance with GMP, FDA, and EMA standards while managing contractors, quality, and project schedules.

CSV & DI Engineer to co-lead efforts aligning site CSV & DI with industry best practices. Responsibilities include providing direction on best practices, overseeing projects, and ensuring quality compliance with FDA/EMA requirements.

Develops and executes global category strategies for Clinical Manufacturing and CMC Product Development services, driving value through supplier relationships and risk management.

Mechanical Piping Superintendent role involving safety, construction, quality, and commercial oversight. Responsibilities include developing work packs, signing off test packs, and coordinating disciplines. Requires 3-5 years' experience and knowledge of piping isometrics and P&IDs.

Experienced Quantity Surveyor/Contracts Manager needed to lead commercial and contractual activities for a pharmaceutical manufacturing facility construction project. Responsibilities include cost control, contract administration, and risk mitigation.

Experienced EHS Advisor needed for pharmaceutical construction. Develop EHS programs, conduct safety inspections, and ensure regulatory compliance. Requires 5+ years in construction EHS and 2+ years in pharma construction.

LOTO Coordinator for electrical systems on construction projects in Belgium. Develops and manages LOTO plans, coordinates isolation, verifies zero-energy states, and ensures compliance with safety regulations and site SOPs.

PM Group seeks an experienced Turnover Coordinator for a pharma construction project in Geel, Belgium. The role involves coordinating the systematic turnover of completed construction systems to commissioning, qualification, and operations teams. Responsibilities include developing turnover packages, managing schedules, facilitating inspections, and ensuring compliance with GMP requirements.

PM Group seeks a Construction PIM to manage asset information throughout its lifecycle. The role involves leading the Information Management team, implementing tagging strategies, and ensuring compliance with industry standards. Requires a Bachelor's or Master's Degree in Engineering or Information Systems and 5+ years of experience as a Project Information Manager.

Experienced EHS Advisor needed for pharmaceutical construction. Responsibilities include developing EHS programs, conducting safety inspections, ensuring regulatory compliance, and managing environmental aspects. Requires a Bachelor's degree and 5+ years of construction EHS experience.

Experienced Quality Lead needed for a major pharmaceutical construction project in Belgium. Responsibilities include implementing quality management systems, ensuring GMP compliance, and managing quality activities throughout construction and validation.