QA Remediation Consultant

Walker Cole International is supporting a UK-based solid oral dose (OSD) pharmaceutical manufacturer in the appointment of an Interim Quality Remediation Consultant.

This is a 3-month, fully on-site contract focused on supporting the delivery of a site-wide quality remediation programme. You will work closely with Quality and Operational teams to implement the remediation plan, strengthen quality systems and ensure regulatory compliance.

Key Responsibilities

• Support the delivery of the site's quality remediation plan.
• Drive remediation activities across the Quality Management System (QMS).
• Review and improve quality processes, procedures and documentation.
• Support CAPA, deviations, investigations and change control activities.
• Track remediation actions and ensure timely completion.
• Collaborate with Quality, Manufacturing and Supply Chain teams to implement improvements.
• Support inspection readiness and regulatory compliance.
• Coach and guide teams through remediation and quality improvement initiatives.

Required Experience & Skills

• Proven experience delivering quality remediation programmes within pharmaceutical manufacturing.
• Strong GMP knowledge, ideally within a solid oral dose (OSD) environment.
• Experience with QMS improvement, CAPA, deviations, investigations and change control.
• Experience supporting regulatory inspections and post-inspection remediation.
• Strong project management and stakeholder engagement skills.
• Comfortable working in a hands-on, fully on-site contract role.

Working Pattern

Fully on-site – UK

Contract Length

3 months

Rate

Competitive day rate, dependent on experience

Keywords

Quality Remediation | GMP | OSD | Pharmaceutical Manufacturing | QMS | CAPA | Deviations | Change Control | Contract | UK