23 qa English-speaking jobs in Breda

We are looking for a Senior Associate QA to provide QA oversight for validation, packaging qualification ... Function as QA SME, collecting input from other QA areas and supporting risk-based decision-making. ... Provide QA support for testing strategies and quality investigations. ... Serve as QA contact for deviation management , especially for technical deviations. ... Act as QA SME (Subject Matter Expert) for risk assessments and support updates and reviews.

As a CW Sr Associate QA, you will perform complaint assessments in accordance with internal procedures ... initiate and manage minor deviations related to Product Complaint Inspection (PCI) activities and act as a QA

Functions as QA SME and collects input from different QA areas to complete the QA assessment for technical ... Deviation management Functions as QA contact for deviation records. ... PASX master data Review and approved master data in PASX system as QA. ... Perform QA oversight for validation of equipment and packaging qualification Perform review and approval

Act as QA SME for deviation records and change control assessments. ... In this role, you are mainly responsible to provide QA oversight for validation of equipment and packaging ... Pay rate- € 25,38 (around 4.170 - 4.376/month) Hybrid: 2-3 days in the office Responsibility: Provide QA

Functions as QA SME and collects input from different QA areas to complete the QA assessment for technical ... Deviation management Functions as QA contact for deviation records. ... PASX master data Review and approved master data in PASX system as QA. ... Packaging / PASX master data) Pharma industry Breda 40 hours per week Accountabilities Perform QA

Functions as QA SME and collects input from different QA areas to complete the QA assessment for technical ... Functions as a QA Contact for deviations records. ... Review and approved master data in PASX system as QA. Change control. ... Orion Group Life Sciences are looking for a Senior Associate QA (GMP) (Validation / Packaging / PASX ... Accountabilities Perform QA oversight for validation of equipment and packaging qualification.

Act as QA SME for deviations and change control processes. ... Provide QA support for validation, testing strategies, and investigations. ... /Bachelor’s degree in Life Sciences, Process Technology, or related field. 3+ years’ experience in QA ... Apply Now If you’re a QA Validation professional ready to make an impact in a GMP-driven environment ... Associate QA (Validation / Packaging / PASX Master Data) to provide quality oversight for equipment validation

Act as QA contact for deviation records and ensure compliance with quality standards. ... Senior Associate QA Breda, reference 2025-01907 Job description We are seeking a Senior Associate ... Ensure GMP compliance for equipment changes and provide QA guidance for technical assessments. ... QA to provide quality oversight for equipment validation, packaging qualification, and PASX master data ... Conduct final QA review of technical change controls and validate assessments from multiple stakeholders

and signing QA statements in GLP studies.Maintenance of the Master Schedule.Evaluation of CAPA plans ... system.Scheduling and performance of study, process, system and facility-based audits according to the QA ... Study Director/Principal Investigator, leading QA and management and follow up on audit responses.Preparing ... member in internal projects.Contribution to acquisition of new projects and public relations.Acting as a QA

Methods transfer, Engineering, Validation, QA, Supply Chain, Maintenance, Manufacturing, etc.).

QA delivers innovative risk-based audit, approaches that provide relevant insights to proactively secure ... Switzerland - Requisition Number: R France, Spain, Poland - Requisition Number: R As a Specialist, QA ... in writing, including writing reports with clarityProvides GCP Audit strategy support, especially on QA ... Clinical Auditor you will:Leads the planning, conduct and reporting of GCP QA routine audits and supports

Methods transfer, Engineering, Validation, QA, Supply Chain, Maintenance, Manufacturing, etc.).

QA delivers innovative risk-based audit, approaches that provide relevant insights to proactively secure ... in writing, including writing reports with clarityProvides GCP Audit strategy support, especially on QA ... work options may be considered on a case-by-case basis and if approved by the Company.As a Specialist, QA ... Clinical Auditor you will:Leads the planning, conduct and reporting of GCP QA routine audits and supports

Collaborate with cross‑functional teams across QA, RA, Packaging, Supply Chain, and Operations.

Collaborating with cross-functional teams (Methods Transfer, Engineering, Validation, QA, Supply Chain

Collaborate with cross-functional teams (i.e., Methods transfer, Engineering, Validation, QA, Supply

Associate Compliance AMGNJP00034697 Breda | QA | CAPA | GMP & GDP | Trackwise | Technical Writing | Your

compliance with GMP and quality standards.Collaborate closely with cross-functional teams including QA

design and functionality Work closely with international and cross-functional teams including UX, QA

Organizing Product Knowledge Product Lifecycle Management (PLM) Program Management Quality Assurance (QA