QC Analyst

Highly Competitive
  1. Permanent
  2. Good Manufacturing Practice (GMP)
  3. United Kingdom
Hatfield, England
Posting date: 03 Nov 2026
71240

Passionate about quality and compliance in pharmaceuticals? Join us and play a key role in ensuring life-changing neurology therapies meet the highest industry standards.

Proclinical is seeking a QC Analyst to join a dynamic team in Hatfield, UK. In this role, you will be responsible for ensuring that all materials are tested according to agreed specifications and procedures while maintaining compliance with industry standards. This position offers an opportunity to contribute to quality control processes in the pharmaceutical sector, focusing on neurology therapies.

Responsibilities:

  • Conduct testing of all materials in accordance with agreed specifications and procedures.
  • Qualify laboratory equipment, including URS, IQ, OQ, and PQ processes.
  • Maintain and calibrate laboratory equipment following approved procedures.
  • Manage laboratory Quality Systems and Quality Management Systems to ensure compliance.
  • Draft Standard Operating Procedures (SOPs) under supervision.
  • Support internal and external audits, including preparation and hosting of inspections.
  • Investigate deviations and implement corrective and preventive actions (CAPAs).
  • Assist with technology transfer projects, particularly QC-related aspects.
  • Implement and manage change control activities.
  • Collect data for Product Quality Reviews (PQRs) and Quality Assurance Performance Indicators.
  • Oversee stability programs and ensure their proper implementation.
  • Perform other duties as requested by the QC Head.

Key Skills and Requirements:

  • Strong knowledge of Quality Control, Quality Assurance, GMP, and regulatory compliance in pharmaceutical manufacturing and packaging.
  • Ability to interpret complex data and present key findings effectively.
  • Proficiency in computer applications such as Word, Excel, and PowerPoint.
  • Demonstrated understanding and application of GMP guidelines and regulations.
  • Excellent communication and presentation skills.
  • Effective time management and problem-solving abilities.
  • Ability to work collaboratively within a team and maintain professional behavior.


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



Apply Now:

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