QC Analyst

Proclinical Consulting; Hatfield; On-site; GBP 28,000 - 38,000; Full time

Job summary

Proclinical is seeking a QC Analyst in Hatfield, UK to ensure tested materials meet specifications and regulatory standards. The role involves qualifying and maintaining lab equipment, managing Quality Systems, and supporting audits and CAPAs.

You will draft SOPs and contribute to technology transfers within a dynamic pharmaceutical environment. The position emphasizes collaboration, accurate data interpretation, and strong communication to uphold GMP in neurology-focused therapies.

Qualifications

• Strong knowledge of GMP, QA, and regulatory compliance in pharma manufacturing.
• Ability to interpret complex data and present findings clearly.
• Proficiency with Word, Excel, and PowerPoint.
• Experience supporting audits and CAPAs.
• Experience with quality systems and technology transfer.

Responsibilities

• Test materials according to specifications and procedures.
• Qualify lab equipment (URS, IQ, OQ, PQ).
• Maintain and calibrate lab equipment as per procedures.
• Manage Quality Systems to ensure compliance.
• Draft SOPs under supervision.
• Support audits and inspections.
• Investigate deviations and CAPAs.
• Assist with QC-related technology transfers.
• Implement and manage change control activities.
• Collect data for PQRs and QA performance indicators.
• Oversee stability programs and ensure proper implementation.
• Perform other duties as requested by the QC Head.

Skills

Quality Control

Quality Assurance

GMP

Regulatory compliance

Data interpretation

Communication skills

Presentation skills

Time management

Problem solving

Team collaboration

MS Word

MS Excel

PowerPoint

Tools

URS

IQ

OQ

PQ

Job description

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.