16 qa English-speaking jobs in Walloon Brabant

QA Operations Specialist – Batch ReviewIn this role, you are responsible for ensuring quality and compliance ... data integrity principles (ALCOA+)Contribute actively to continuous improvement initiatives within QA ... You work closely with Production, QA, and QC to ensure that batch documentation and processes meet applicable ... GMP-regulated pharmaceutical manufacturing environmentProven hands-on experience in batch record review within QA ... detail-orientedProactive and comfortable working in a fast-paced manufacturing environment What we offer:A challenging QA

advice, support and management for technical operational QA and general QA matters associated with vendors ... #39;Alleud, Belgium .About The Role This position provides leadership and in-depth Quality Assurance (QA ... ) expertise to drive strategic and operational QA activities associated with Vendors engaged in preclinical ... ; work closely with Corporate QA teams, functional areas and affiliates across geographies.Be a Best ... record retention, audit rights).Support the Deviation & Escalation team (lead contact) by providing QA

requirements through close collaboration with vendor QA teams and UCB Technical Operations. ... It also provides internal QA consultancy and ensures compliance with MDR, ISO standards, and GMP/cGMP ... The position also works in partnership with affiliate and operational teams to ensure effective QA service ... approve deviations Track CAPA events and closure Oversee/track change controls Act as the Operational QA ... medical devices, combination products, and primary packaging, and internal stakeholders such as Corporate QA

Mission Join our Operational Quality team to strengthen Environmental Monitoring (EM) and QA ... Key Responsibilities • QA Oversight Design & Execution – Build and roll out oversight plans, workflows ... experience. • 4–6 years in a cGMP pharmaceutical/biotech environment, including ≥3 years focused on QA

Collaborate and interact with Quality Assurance (QA) and Regulatory Affairs (RA) departments. ... Proven ability to effectively collaborate and interact with Quality Assurance (QA) and Regulatory Affairs

Partner with IT, QA, Patient Safety, Clinical, R&D, and Automation teams. ... What you will do Quality Oversight & Compliance Provide senior‑level QA oversight for the full lifecycle ... Facilitate cross-functional decision-making and serve as a key QA representative in system-related projects ... Project & Stakeholder Management Provide QA guidance to project teams during system implementation, upgrades

We have extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions

understanding: Without being a developer, you understand the software lifecycle (CI/CD, environments, QA

required.Stakeholder CollaborationWork closely with internal stakeholders (Operations, Technical Services, QA

through October 2026 business go-live Integration Management Coordinate with Supply Chain, QA

processes and effectiveness, Partner with the UCB Network QA operational teams to prepare sites for ... committees, Lead improvement initiatives, identified by Senior Management, in-order to improve Corporate QA

Collaborate closely with discovery scientists, CMC, QA, and external CDMOs to ensure alignment and future

Send the material certificates to QA (reports and as-built drawings).

Send the material certificates to QA (reports and as-built drawings).

discovery teams and participate as a subject matter expert within cross-functional groups (e.g., CMC, QA

Management and the wider GXP Global Quality Auditing group, including outsourcing partners and senior QA