14 Quality Engineering jobs in Brussels.

Hiring now: Spec Plant Qaqualified Pe @ Amgen, Quality Engr @ Bd, Sr Ops Dir Drug Substance @ Johnson Jo, Veeva Vault Consultant @ Cognizant, Sr Mgr Technical Services @ Steris, Sterility Assurance Sr Mg @ Novo Nordi, Prod Assessor @ Sgs.Explore more at jobswithgpt.com.

🔥 Skills

compliance (3) regulatory compliance (3) continuous improvement (2) cross-functional teams (2) project management (2) contamination control (2) AVEVA System Platform (2) automation (2) incident management (2) problem management (2)

📍 Locations

Brussels (7) Antwerpen (4) Breda (1) Temse (1) Geel (1)

Amgen

Skills & Focus: Quality Assurance, Compliance, GMP, Manufacturing, Pharmacy, Clinical Research, Supply Chain, Validation, Change Control, Audit
About the Company: Amgen is one of the world's leading biotechnology companies, dedicated to serving patients by researching, manufacturing, and delivering high-quality products …
Experience: Previous experience in processes involved in clinical and commercial manufacturing (GMP), warehousing, supply chain, equipment engineering principles, and validation.
Type: Full time

Bd

Skills & Focus: quality assurance, temperature management, inspections, regulatory requirements, MDR, IVDR, continuous improvement, cross-functional teams, CAPA, document management
About the Company: BD is one of the largest global medical technology companies in the world, advancing the world of health™ by improving medical discovery, diagnostics, and the …
Experience: Minimum of 3 years of experience in QA/QC, preferably in distribution or manufacturing
Salary: Competitive
Type: Full-Time
Benefits: Healthcare, 401(k)/ Retirement Plans, Professional Development, Paid Time Off, Awards & Recognition

Johnson & Johnson

Skills & Focus: Supply Chain Manufacturing, Plant Management, Drug Substance, Production Output, Quality Compliance, EHS, Leadership, Operational Strategy, Continuous Improvement, Team Development
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: Minimum of 15 years of experience in a pharmaceutical manufacturing environment.
Type: Fully Onsite
Skills & Focus: technology leadership, supply chain, product development, cell therapy, gene therapy, program management, cross-functional, ERP, stakeholders, compliance
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: 10+ years of experience in technology product management and/or technical program management
Type: Full-time

Cognizant

Skills & Focus: Veeva Vault, Veeva RIM, Veeva Quality, Veeva Clinical, technical leadership, software development life cycle, agile methodologies, troubleshooting, project management, regulatory compliance
About the Company: Cognizant is one of the world's leading professional services companies, transforming clients' business, operating, and technology models for the digital era. …
Experience: Extensive experience with the Veeva Vault platform and its modules (Veeva RIM, Veeva Quality, Veeva Clinical)
Salary: competitive salary based on your qualities and experience
Type: Full-time
Benefits: 32 days of paid holiday per year, a car allowance, a laptop and a smartphone, a pension scheme, and hospitalization ins…

Steris Corporation

Skills & Focus: technical services, contamination control, validation, pharmaceutical, biopharmaceutical, project management, customer support, stakeholder communication, microbiology, cleanroom environments
About the Company: STERIS is a leading global provider of products and services that support patient care with an emphasis on infection prevention.
Experience: Twelve or more years related work experience.
Type: Full-time

Cognizant

Skills & Focus: AVEVA System Platform, automation, IT support, incident management, problem management, change management, application operations, Pharma 4.0, GAMP, ISA 88
About the Company: Cognizant is a global leader in delivering digital transformation solutions across various industries, with expertise in areas such as Automation, MES & Digita…
Experience: 5+ years
Type: Full-time

Novo Nordisk

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.
Skills & Focus: Post Merger Integration, Production Support, Stakeholders, Project Management, Change Management, Risk Management, Aseptic Manufacturing, Collaboration, Diagnostics, Analytical Skills
About the Company: Novo Nordisk is a global healthcare company with more than 100 years of innovation and leadership in diabetes care. They also have a strong commitment to devel…
Experience: 10 years of relevant experience within project management.
Benefits: Novo Nordisk values its employees for their unique skills and makes room for diverse life situations, aiming to create …

Cognizant

Skills & Focus: AVEVA System Platform, automation, IT Engineer, pharmaceutical industry, incident management, problem management, change management, application operations, GAMP, ISA 88
About the Company: Cognizant is one of the world's leading professional services companies, transforming clients' business, operating, and technology models for the digital era. …
Experience: 5+ years relevant industry experience
Type: Full-time

Sgs

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.
Skills & Focus: Product Assessor, Active Medical Devices, technical documentation review, EU regulations, cross-functional teams, recruitment, KPI monitoring, training development, technical queries, medical devices certification
About the Company: A dynamic team focused on certification in the medical device sector.
Experience: Strong background as a Product Assessor within an EU notified body conducting MDD/MDR technical documentation review
Type: Full-time