Location: Munich and flexible working
Our client is a clinical contract research organization (CRO) working from Phase I-IV delivering full-service across pharma, biotech and medical device sectors. They seek a QA Auditor to join their team in a variety of European locations, providing audit partnering to their international clients- post COVID this role will involve up to 50% travel.
Plan and execute internal system audits and external investigative site/vendor audits
Create, maintain, and revise departmental SOPs, forms, and templates
Coordinate, conduct, and track company-wide Regulatory Training (ICH/GCP, GLP, Medical Device)
Develop training materials and applicable tests and guides
Coordinate, conduct, track, and resolve CAPA investigations
Work with outside clients/sponsors and as a trusted partner with internal operations to promote a culture of continuous improvement
Essential Skills and Qualifications:
Bachelor’s degree in life sciences or nursing
Minimum 1 year experience in a QA department in pharma, biotech or medical devices
Experience of GCP site audits
Excellent written and verbal communication skills
Exceptional teamwork skills but also ability to work independently
This role is based in Munich, Leuven or Warsaw with extensive travel but will support flexible working on a part-remote basis, with 8 days a month from home going forward.
The benefits package includes medical insurance, dental and pension.
Please apply today to be considered or contact Katie Dunbar on +44 (0)1293 584300 or email@example.com for more information.
Salary: Competitive + Generous benefits package
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