QC Analyst

TN United Kingdom; Hatfield; On-site; GBP 30,000 - 40,000; Full time

Job summary

A global pharmaceutical company in Hatfield is seeking a QC Analyst for a 1-year fixed-term contract. The role involves testing materials, maintaining quality systems, and supporting audits. Ideal candidates will have extensive knowledge of quality control and regulatory compliance.

Qualifications

• Extensive knowledge of Quality Control, Quality Assurance, and GMP.
• Ability to establish effective working relationships.

Responsibilities

• Test all materials according to specifications.
• Maintain and calibrate laboratory equipment.
• Support internal and external audit processes.

Skills

Communication

Technical Judgment

Data Interpretation

Education

Pharmaceutical Manufacturing Knowledge

Quality Control Knowledge

Tools

Word

Excel

PowerPoint

Job description

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Job Opportunity: QC Analyst

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

Role:

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

Key Duties:

1. Test all materials according to agreed specifications and procedures.
2. Qualify all laboratory equipment.
3. Maintain and calibrate all laboratory equipment according to approved procedures.
4. Maintain all laboratory Quality Systems and Quality Management Systems in compliance with approved procedures.
5. Assist in writing SOPs related to QC support under supervision.
6. Support internal and external audit processes and schedules.
7. Assist in the preparation and hosting of competent authority inspections.
8. Investigate deviations and support CAPA processes.
9. Collect data for reporting Quality Assurance Performance Indicators.
10. Support the implementation and management of stability programmes.
11. Perform other duties as requested by the QC Head.

Candidate Background:

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