25 English-speaking jobs in Geel

Director of Forecasting, Randomization & Trial Supply Management drives digital transformation strategy for clinical kit forecasting and RTSM. This role leads multi-functional teams to modernize supply chain processes within R&D.

Define, standardize, and improve the delivery methodology for Transcend, a global transformation program consolidating ERP systems. Own program methodology across a multi-release environment, ensuring consistent standards and governance.

Lead early design inputs and technical strategy for synthetic drug substance (API) manufacturing processes. Provide expertise in unit operations like chemical reaction, crystallization, and filtration, ensuring cGMP compliance and process safety.

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 MD with post-doctoral training and 7+ years of clinical research experience, including 3+ years in phase II/III development.

Director, Medical Device Interface, Regulatory Affairs provides strategic regulatory leadership for medical devices in medicinal product development. This role requires deep global expertise in device regulations and experience leading device-related regulatory strategies.

Director, Business Readiness and Change leads a global transformation to modernize transactional processes into a standardized ERP platform. This role involves shaping business readiness strategies, advising senior leaders, and leading change artifacts.

Director, Global Advanced Therapies Planning leads end-to-end global CAR-T planning, including Supply, Demand, and Inventory Management. This role manages a team of 30 across multiple sites.

Director, Strategic Business Transformation leads strategic assignments, providing decision-focused insights for Therapeutics Development and Supply. Requires 10-12 years in consulting or strategy within the biopharmaceutical industry.

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.

Lead Software Engineer for R&D Technology designs and delivers solutions for next-gen R&D capabilities. This role bridges scientific needs with scalable technology, owning architecture, CI/CD, and integration across lab systems.

Construction Manager role requires 10+ years in mechanical projects within pharmaceutical or oil and gas industries. Responsibilities include onsite coordination, schedule monitoring, and subcontractor supervision.

Manage mechanical project execution, ensuring safe, efficient delivery to high quality standards. Responsibilities include planning, team management, subcontractor scope, and progress reporting. Requires prior mechanical project management experience.

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.

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.

The Director will develop and execute global category strategies for Clinical Manufacturing and CMC Product Development services, driving value through strategic supplier relationships and risk management.

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.

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.

EHS Advisor needed for pharmaceutical construction project in Geel. Develop and implement EHS programs, conduct safety inspections, ensure regulatory compliance, and investigate incidents. Requires a bachelor's degree in a related field, 5+ years of construction EHS experience, and 2+ years in pharmaceutical or regulated industry construction.

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.