38 English-speaking jobs in Geel

MSAT Scientist with expertise in upstream cell culture processes needed for technology transfer, process optimization, and support of commercial manufacturing. Requires a Master's or PhD in Life Sciences and 3-5 years of relevant experience.

Quality Scientist I needed for technology transfer of new products and processes to GMP manufacturing. Focus on upstream cell culture with support for existing commercial processes. Requires MS or PhD in Life Sciences with 3+ years (PhD) or 5+ years (MS) experience in MSAT, process development, or similar.

MSAT Scientist with expertise in upstream cell culture processes needed for technology transfer, process optimization, and support of commercial manufacturing. Requires a Master's or PhD in Life Sciences and 3-5 years of relevant experience.

MSAT Scientist needed for innovative biopharmaceutical organization. Focus on upstream cell culture, technology transfer, process optimization, and support for commercial manufacturing. Requires Master's or PhD in Life Sciences with 3+ years (PhD) or 5+ years (Master's) experience in MSAT, process development, or similar. Strong analytical skills, GMP knowledge, and experience with mammalian cell culture are essential.

Electrical Supervisor to lead and coordinate teams on a major pharmaceutical construction project in Geel, Belgium. Evening shift. Requires experience in electrical installations, GMP, and cleanroom standards.

Experienced Mechanical Supervisor needed for evening shift on a pharmaceutical construction project in Geel, Belgium. Responsibilities include supervising installation teams, ensuring GMP compliance, coordinating with construction teams, and managing contractors. Minimum 5 years supervisory experience in mechanical installations, pharmaceutical or cleanroom construction experience preferred. Strong leadership and communication skills required. Fluent English required, Dutch/Belgian language skills advantageous. Valid EU work authorization and flexibility to work evening shifts on site.

Supports the safe and compliant execution of analytical activities for raw materials, packaging, intermediates, APIs, and drug product intermediates. Coordinates investigations, performs root cause analyses, and contributes to continuous improvement initiatives.

Site Document Controller needed for a 2-year contract in Belgium. Manage document distribution, maintain registers, issue transmittals, and support site administration. Requires administration experience, strong communication, and proficiency in Microsoft Office.

Experienced CSA Package Owner/Lead to manage civil, structural, and architectural design for a pharmaceutical manufacturing facility. Responsibilities include leading multidisciplinary teams, ensuring compliance with industry standards, and managing project budget and timeline.

Administers contracts for mechanical systems (HVAC, piping, utilities) on a pharma construction project. Reviews submittals, tracks variations, and verifies contractor payments. Requires a mechanical engineering degree and 5+ years' experience in contracts administration for mechanical installations.

Material Handler II will pick, pack, and label chemicals accurately while adhering to safety procedures and quality standards. Experience in a manufacturing, operations, production, or lab setting is required.

Experienced Mechanical Piping Supervisor needed for pharma construction project. Supervise piping installation teams, ensure quality installation of various piping systems, and coordinate with trades. Manage material logistics, oversee testing, and report progress. Strong knowledge of piping regulations, GMP requirements, and sterile systems is essential.

HVAC & Sprinkler Package Owner for large-scale pharma project. Leads projects from a Building Services and Mechanical perspective, analyzes engineering problems, and provides support to budget proposals. Requires 5+ years of experience in heavy industrial engineering design, Chartered or working towards same. Experience in 2D CAD and 3D Revit/Cadworks design projects is preferred.

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 standards.

PM Group seeks an experienced Package Owner to lead and manage cleanroom and finishes delivery for a pharmaceutical manufacturing facility. Responsibilities include overseeing design coordination, contractor management, and ensuring compliance with EU GMP and Belgian regulations.

PM Group seeks an experienced E&I Package Owner to lead electrical and instrumentation package delivery for a pharma manufacturing facility. Responsibilities include design coordination, contractor management, system installation, and compliance with industry standards.

Experienced EHS Advisor needed for pharmaceutical construction project. Develop and implement EHS programs, conduct safety inspections, ensure regulatory compliance, and investigate incidents.

The Director EH&S for the Geel MAKE site is responsible for overseeing and managing EHS activities across the site, ensuring compliance with regulations and the safety of employees, visitors, and contractors. This role leads a team of EH&S professionals, develops and implements site EH&S strategies, and manages the site EHS function, including budgets, resource allocation, and performance. The Director EH&S is accountable for overall site performance, including compliance, risk reduction, and management initiatives.