Pharma QC Analyst: Quality & Compliance Specialist

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

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.