Proclinical is currently working alongside a pharmaceutical company who is seeking a full-time QA GCP Auditor to join their team. This role is pivotal in supporting our European activities and contributing to the company's success. If you have a background in GCP and are looking for an opportunity to grow and develop your career, this could be the perfect fit for you.

Please note that to be considered for this role you must have the right to work in this location.

Responsibilities:

Partner with client operations to foster a culture of continuous improvement.Coordinate and conduct internal system audits and external investigative site/vendor audits.Create, maintain, and revise departmental Standard Operating Procedures, forms, and templates.Develop training materials and applicable tests and guides.Collaborate with outside clients and sponsors.Host Sponsor audits and Regulatory Inspections.Act as QA Project Leader, managing timelines and coordinating workload among QA Auditors.

Key Skills and Requirements:

Bachelor's degree in life sciences or nursing.Experience in a QA GCP department within a related industry.Proficiency in conducting GCP site audits and vendor audits is highly preferred.Excellent written and verbal communication skills.Strong teamwork abilities.Capability to work independently.Willingness to travel approximately 50% across Europe.

If you are having difficulty in applying or if you have any questions, please contact Ingrid Aymes at i.aymes@proclinical.com

Apply Now:

If you are interested in learning more or applying to this exciting opportunity, please complete the form below and attach a copy of your CV. Alternatively, for further details or to talk directly to a life sciences recruitment specialist, please request a call back at the top of this page.

Proclinical is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Proclinical is acting as an Employment Agency in relation to this vacancy.