Last updated: 2025-05-22

20 Quality Assurance And Engineering jobs in Brussels.

Hiring now: Operational Quality Mgr O @ Sgs, Qa Qualification Engr Pro @ Johnson Jo, Regulatory Affairs Proj M @ Perrigo, Production Mgr @ Novo Nordi, Validation And Qualificat @ Alten, Sr Principal Engr @ Baxter, Research Scientist Ii Cli @ Baxter Hea, Software Verification Mgr @ Baxter Int.Explore more at at kaamvaam.com

🔥 Skills

Quality Assurance (4) compliance (4) GMP (4) CAPA (3) risk assessment (3) Compliance (3) team leadership (3) validation (3) continuous improvement (3) regulatory compliance (3)

📍 Locations

Gent (6) Braine-l'Alleud (6) Brussels (4) Antwerpen (3) Mechelen (1)

Sgs

Skills & Focus: quality management, CRO, clinical trials, quality system, SOPs, non-conformance, CAPA, process improvements, risk assessment, cross-functional

Johnson & Johnson

Skills & Focus: Qualification Engineer, Process Equipment, Quality Assurance, Supply Chain Engineering, cGMP regulations, FDA/EU guidance, calibration, compliance, risk assessment, collaboration
About the Company: At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented,…
Experience: Experience required in quality assurance and engineering
Type: Full-time
Skills & Focus: quality assurance, investigations, deviations, complaints, CAPA, inspection, audit, batch documentation, GMP, ATMP
About the Company: A global healthcare company focused on innovative medicine and MedTech solutions to improve health worldwide.
Experience: At least 3 years in the pharmaceutical industry
Type: Full-time
Skills & Focus: Quality Assurance, Manufacturing Execution Systems, CAR-T, Automation, Validation, Compliance, Pharmaceutical Industry, GMP, Risk Assessment, Quality Standards
About the Company: Johnson & Johnson is a major American multinational corporation in the pharmaceutical, medical devices, and consumer goods industry.
Experience: At least 2 years of cross-functional experience in the pharmaceutical industry.
Type: Hybrid

Perrigo

Skills & Focus: Regulatory, Product, Approval, Lifecycle, Labeling, Compliance, Documentation, Submission, Market access, Project management
About the Company: Perrigo is a top 10 European consumer self-care market player and the largest U.S. store brand provider of OTC and infant formula, dedicated to providing trust…

Johnson & Johnson

Skills & Focus: industrial automation, project management, stakeholder engagement, problem resolution, GxP compliance, innovation, team leadership, communication skills, pharmaceutical sector, data integrity
About the Company: At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented,…
Experience: Proven experience in a GxP-regulated environment.
Type: Hybrid

Perrigo

Skills & Focus: Quality Assurance, regulations, GMPs, GMP, ISO 9001, ISO 13485, validation, audit, CAPA, regulatory
About the Company: Perrigo is a leading provider in the European Consumer Self-Care market and the largest U.S. store brand provider of over the counter and infant formula, commi…

Novo Nordisk

Skills & Focus: aseptic manufacturing, people management, quality standards, continuous improvement, performance optimization, GMP compliance, team leadership, audits management, stakeholder collaboration, operational excellence
About the Company: Novo Nordisk is its people. We know that life is anything but linear and balancing what is important at different stages of our career is never easy. That’s wh…
Experience: Minimum 10 years of experience in aseptic GMP manufacturing, with at least 4 years in people management

Alten

Skills & Focus: validation, qualification, pharmaceuticals, health-related products, project planning, risk assessment, Functional Specifications, Design Specifications, protocols, training programs

Novo Nordisk

Skills & Focus: validation, CSV, regulatory compliance, equipment qualification, GMP, pharmaceutical, validation projects, automated instruments, system decommissioning, continuous improvement
Skills & Focus: Sterility Assurance, contamination control, GMP Pharmaceutical Manufacturing, team leadership, quality standards, compliance, continuous improvement, microbiological controls, regulatory inspections, performance management
About the Company: Novo Nordisk is its people. We know that life is anything but linear and balancing what is important at different stages of our career is never easy. That’s wh…
Experience: Minimum 10 years of experience in Sterility Assurance, or contamination control (Microbiology) within GMP Pharmaceutical Manufacturing. At least 5 years of leadership experience in sterile manufacturing.

Baxter

Sr Principal Engineer Braine-l'Alleud
Skills & Focus: Polymer, Material Sciences, Medical Devices, Product Requirements, Traceability, Product Risk Management, Verification & Validation, Project Management, Mechanical Testing, Design History File
About the Company: Baxter's Research and Development teams work cross functionally to innovate, develop and introduce creative solutions for patients needs globally. The company …
Experience: Professional with experience in Polymer, Material Sciences, Medical Devices.
Benefits: Support for Parents, Continuing Education/ Professional Development, Employee Health & Well-Being Benefits, Paid Time O…
Skills & Focus: stability studies, cGMP, regulatory compliance, GxP, experimental design, project management, statistical analysis, quality systems, collaborative, medical innovations
About the Company: Baxter is a global healthcare leader dedicated to saving and sustaining lives through innovative solutions in medical devices and therapies.

Baxter Healthcare Corporation

Skills & Focus: Research, Development, Clinical Nutrition, Technical Lead, Project Management, Regulatory Compliance, Innovative Solutions, GxP Regulations, Quality System Regulations, Team Leadership
About the Company: Baxter's Research and Development teams work cross functionally to innovate, develop and introduce creative solutions for patients' needs globally. With over 8…
Experience: Bachelor's degree in a scientific field with at least 15 years of relevant experience, MS with at least 10 years, or PhD with at least 4-6 years of relevant experience.
Benefits: Support for Parents, Continuing Education/Professional Development, Employee Health & Well-Being, Paid Time Off, 2 Days…

Baxter

Skills & Focus: Change Management, Regulatory Standards, Quality Assurance, Documentation, Risk Assessment, Product Development, Cross-functional Collaboration, Compliance, Design Control, Clinical Nutrition
About the Company: A global healthcare company specializing in medical devices and therapies, dedicated to improving patient outcomes through innovative products and solutions.

Baxter International

Skills & Focus: Software Verification, Engineering, Medical Devices, R&D, Product Security, Embedded Software, Electromechanical, Integration, Healthcare, Innovation
About the Company: Baxter International is a leading manufacturer of medical devices and solutions, focusing on innovative therapies and healthcare solutions for patients worldwi…
Type: Full Time
Benefits: Our comprehensive benefits options reflect the value we place in our employees.

Baxter

Skills & Focus: innovation, regulatory, compliance, projects, product design, quality, reliability, technical, leadership, regulations
About the Company: Baxter's Research and Development teams work cross functionally to innovate, develop and introduce creative solutions for patients needs globally. From Scienti…
Experience: at least 15 years of relevant experience (Bachelor's), 10 years (MS), or 4-6 years (PhD)
Benefits: Support for Parents, Continuing Education/ Professional Development, Employee Health & Well-Being Benefits, Paid Time O…

Sgs

Skills & Focus: quality system, audits, accreditation, certification, improvement measures, procedures, quality controls, internal audits, external auditors, reporting
Skills & Focus: Cardiovascular, Soft Tissue, technical file reviews, European Medical Device Regulation, Medical Device Directive, UKCA, Class IIa, Class IIb, Class III, CE marking
Skills & Focus: Final Review, Certification, MDD 93/42 EC, MDR (EU) 2017/745, QMS, technical documentation, audit packs, compliance, certificate issuance, regulatory compliance
About the Company: SGS is a leading inspection, verification, testing and certification company.