QA Auditor

Location: London and flexible working

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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 London, providing audit partnering to their international clients- post COVID this role will involve up to 50% travel.

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Role Responsibilities:

• 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 London 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, pension and access an on-site gym and pool.

Please apply today to be considered or contact Katie Dunbar on +44 (0)1293 584300 or katie.dunbar@rbwconsulting.com for more information.

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Salary: £60,000 Per annum + Benefits