QA Officer

Eurofins Scientific - Nederland; Breda; On-site; EUR 40,000 - 60,000; Full time

Job summary

Eurofins Scientific - Nederland is seeking a QA Officer to ensure quality assessments and compliance within their operational processes. The role involves planning audits, reviewing compliance with guidelines, and improving quality procedures.

The ideal candidate should have at least 2 years’ experience, a relevant Bachelor degree, and strong analytical and organizational skills. The position is based in Breda, Netherlands, within a dynamic global organization.

Qualifications

• At least 2 years of relevant work experience in QA.
• Strong affinity with GCLP and/or GCP quality systems.
• Experience in ISO/IEC 17025 and 15189.

Responsibilities

• Perform quality assessments and advise on improvements.
• Plan and execute audits according to procedures.
• Review raw data for compliance with guidelines.

Skills

Quality Systems Knowledge

Analytical Skills

Persuasiveness

Organizational Talent

Education

Bachelor degree in Life Science or Quality related education

Job description

Eurofins Central Laboratory is a dynamic, global organization dedicated to providing global central laboratory services to support all phases of clinical trials. As part of Eurofins Scientific, one of the world’s leading laboratory organizations, it offers end-to-end testing solutions in the industry. Eurofins Central Laboratory is setting new standards with GLP capabilities embedded within its Central Laboratory and supports customers with laboratory facilities in the USA, Europe, Singapore and China, and a back office in India.

Eurofins Central Laboratory is looking for a QA Officer.

Job Description

The QA Officer is responsible for acting as a QA coordinator within the organization, performing quality assessments on the operational processes and advising on improvements towards the departments.

Key Accountabilities

• Plan, execute and report audits according to the audit timetable and applicable procedures.
• Plan and execute protocol, laboratory and supporting data, and final report (interim, draft, final) audits and conduct in-life phase inspections as required for compliance with internal procedures and bioanalytical method validation guidelines (FDA, EMA).
• Perform review of raw data against the draft reports of bioanalytical studies to verify that the reports accurately and completely reflect the raw data generated.
• Monitor the progress, appropriateness and correct implementation of corrective measures.
• Prepare, review and improve QA procedures.
• Review and approve procedures of other departments within the organization.
• Provide quality-enhance training on your own initiative and on request.
• Act as a contact person for quality questions from the organization.
• Assist with the preparation and hosting of client audits and/or regulatory inspections.
• Review and evaluate adequacy of investigations and CAPA (corrective actions/preventive actions) reports.
• Maintain current knowledge of standard requirements according to GCLP, GCP, GMP, CAP, ISO17025 and ISO 15189 guidelines related to the business process.
• Archive and document control duties as assigned by QA Manager.
• Perform other related tasks that match training and experience on request of the QA Manager.

Qualifications

• At least 2 years’ relevant work experience.
• Experience with or strong affinity with quality systems set up according to GCLP and/or GCP.
• Work experience in the field of ISO / IEC 17025 and 15189 is a pré.
• Bachelor degree in Life Science or a Quality oriented education or MLO education with HLO work and think level.
• Confident to engage in the discussion with the management.
• Excellent command of English, spoken and written.
• Able to increase the quality consciousness of employees by your persuasiveness.
• Strong analytical skills.
• Organizational talent, continue to perform effectively under pressure and know how to monitor progress.