探花合集

QA GCP Manager

Highly Competitive
  1. Permanent
  2. Good Clinical Practice (GCP)
  3. United Kingdom
City of London, England
Posting date: 15 Jun 2026
69899

Are you looking to drive groundbreaking quality assurance and make a real impact? Join our client and lead the way in advancing clinical quality assurance!

探花合集 is looking for a Quality Assurance Manager to join a dynamic organization on a permanent basis in the UK. This role offers flexible home and/or office working, industry leading training, and a competitive total reward package.

The primary purpose of this role is to support the Director of Quality & Compliance in delivering Quality Assurance activities and overseeing, maintaining, and improving the Quality Management System (QMS). You will play a key role in ensuring compliance with applicable regulations and internal procedures, supporting audits and inspections, contributing to continuous improvement initiatives, and promoting a culture of quality across the business. This role provides an opportunity to take ownership of key QA processes and collaborate closely with stakeholders across the organization to drive high standards of quality and compliance.

Responsibilities:

The tasks listed below outline the scope of this position. The application of these tasks may vary based on current business needs.

Quality Assurance:

  • Manage the Quality Management System (QMS).
  • Contribute to the generation and management of the internal audit schedule.
  • Independently conduct and report audits in accordance with the internal audit schedule.
  • Conduct vendor audits as instructed.
  • Lead, manage, and coordinate client audits and regulatory inspections.
  • Respond to and follow up on audit reports and vendor questionnaires.
  • Review and provide QA approval of SOPs and other controlled documents.
  • Effectively monitor compliance with processes.
  • Provide input for and maintain oversight of CAPAs and quality issues.
  • Generate quality metrics reports to update the management team on quality-related issues and initiatives.
  • Ensure company-wide compliance with EU and UK clinical trial legislation, ICH GCP, and other applicable regulations.
  • Perform QA reviews of Computerized Systems Validation (CSV) projects.
  • Conduct risk assessments where required.

Quality Improvement:

  • Promote good practices by challenging existing standards and suggesting areas for improvement.
  • Inspire and drive the organization to achieve and maintain quality values.
  • Review lessons learned from meetings, customer concerns, issues, and CAPAs for quality-related items, and coordinate any resulting training or process updates.

Training and Development:

  • Develop, coordinate, and deliver training materials related to quality, including GCP.
  • Perform work in full compliance with applicable legislation, regulations, company policies, procedures, and training.

Data Protection:

  • Assist the Data Protection Officer (DPO) with data protection activities.
  • Ensure adherence to applicable legislation, including GDPR.

Information Security:

  • Assist in hosting ISO27001 accreditation and subsequent surveillance audits.
  • Review SOPs for information security compliance and draft new SOPs/policies as required.
  • Conduct internal and vendor information security audits.
  • Support information security assessments of the organization.
  • Conduct information security assessments of potential vendors.
  • Assist with managing potential and actual data breaches in conjunction with relevant teams.

Key Skills and Requirements:

  • Training and proven years of working experience in Good Clinical Practice (GCP).
  • Professional working years of relevant QA experience, preferably within the life sciences sector.
  • Other Information/Additional Requirements:
  • Expert knowledge of UK, EU, and US clinical trial legislation.
  • Strong ability to communicate effectively and influence across and within the organization.
  • Excellent written and verbal communication skills.
  • Exceptional interpersonal and negotiation skills.

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

If you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists please request a call back at the top of this page.

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

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