QC Analyst

TieTalent; Hatfield; On-site; GBP 30,000 - 45,000; Full time

Job summary

A global pharmaceutical company in Hatfield is seeking a QC Analyst on a 1-year fixed-term contract. The role involves testing materials, maintaining quality systems, and supporting audits. Ideal candidates will have strong knowledge of Quality Control and GMP guidelines.

Qualifications

• Extensive knowledge of Quality Control and Assurance in pharmaceuticals.
• Proficiency in interpreting complex data and presenting findings.

Responsibilities

• Testing materials according to specifications and procedures.
• Maintaining compliance of laboratory Quality Systems.
• Supporting internal and external audits.

Skills

Quality Control

Quality Assurance

GMP

Regulatory Compliance

Technical Judgment

Data Interpretation

Tools

Word

Excel

PowerPoint

Job description

CK Group - Science, Clinical and Technical

CK Group is recruiting for a QC Analyst to join a well-established and successful global pharmaceutical company based in Hatfield, Hertfordshire, on a 1-year fixed-term contract.

Role:

This position is responsible for ensuring that all materials are tested according to agreed specifications, procedures, and within specified lead times.

Key duties will include:

1. Testing all materials according to specifications and procedures.
2. Qualifying and calibrating laboratory equipment according to approved procedures.
3. Maintaining and ensuring compliance of all laboratory Quality Systems and Quality Management Systems.
4. Writing SOPs related to QC support under supervision.
5. Supporting internal and external audits and audit schedules.
6. Assisting with preparation and hosting of authority inspections.
7. Investigating deviations and supporting CAPA processes.
8. Collecting data for Quality Assurance Performance Indicators.
9. Implementing and managing stability programmes.
10. Performing other duties as assigned by the QC Head.

Your Background:

• Ability to establish effective working relationships and communication within organizations and with clients.
• Extensive knowledge of Quality Control, Quality Assurance, GMP, Regulatory Compliance, and pharmaceutical manufacturing and packaging.
• Strong technical and scientific judgment.
• Ability to interpret complex data and present key findings.
• Proficiency in computer applications such as Word, Excel, and PowerPoint.
• Knowledge and application of GMP guidelines and regulations.

Apply:

Applicants must have the entitlement to work in the UK. Please quote the job reference (Apply online only) in all correspondence.