9 qa English-speaking jobs in Breda

Associate QA to ensure quality oversight within the clinical supply chain. ... Associate QA - Clinical Manufacturing / Supply Chain Location: Breda, full time 40 hours Hybrid. ... In this role, you'll provide QA support for clinical trial products received and shipped to clinical ... and regulatory compliance Preparation of monthly quality metrics Cross-functional issue resolution QA ... Bachelor's degree in Life Sciences or related field Minimum of 3 years of QA or manufacturing experience

Associate QA – Clinical Manufacturing & Supply Chain (Level 4) Breda, Netherlands – Full-time Company ... Associate QA, you will provide quality oversight across clinical manufacturing and supply chain operations ... improvement initiatives Requirements: Bachelor’s degree in Life Sciences or related field 3+ years’ QA ... issues in manufacturing and transport Review and approve deviations, SOPs, and work instructions Provide QA

Associate QA clinical supply chain, you will be responsible for providing QA oversight on the supply ... Execute QA compliance checks. What do you need to be successful in this role? ... In this role, you will provide QA support for clinical products received and distributed from ABR to ... Associate QA, you are mainly responsible to provide quality guidance for Investigational Medicinal Products ... assuring that GDP and GMP standards are maintained, and to support Clinical QA primary processes: Responsible

Associate QA, you will provide quality oversight for the clinical supply chain and support production ... Your key responsibilities include: QA support for Investigational Medicinal Products, ensuring GDP and ... SOP review to ensure alignment with corporate, site, and regulatory standards Preparation of monthly QA

between ABR and ATO Clinical Customer Service (CCS) teams, Development Supply Chain (DSC) stakeholders, QA

Support and work with QA: to ensure timely resolution of corrective actions from audit findings for your

Support and work with QA: to ensure timely resolution of corrective actions from audit findings for your

Support and work with QA: to ensure timely resolution of corrective actions from audit findings for yourown

-Support regulatory inspections (e.g., FDA/EMA) and collaborate with QA, Validation, Supply Chain, Engineering