QC Analyst

CK Group; 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 laboratory equipment, and ensuring compliance with quality systems. Ideal candidates will have extensive knowledge of GMP and Quality Control, along with strong communication and technical skills.

Qualifications

• Extensive knowledge of Quality Control 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 Judgement

Data Interpretation

Tools

Word

Excel

PowerPoint

Job description

CK Group are 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 job is responsible for ensuring that all materials are tested according to agreed specifications and procedures and within agreed lead times.

Key duties will include :

• To test all materials according to agreed specifications and procedures.
• To qualify all laboratory equipment.
• To maintain and calibrate all laboratory equipment according to approved procedures.
• To maintain all laboratory Quality Systems and Quality Management Systems in compliance according to approved procedures.
• To write under supervision, all SOPs associated with QC support.
• To support the internal and external audit process and audit schedules as appropriate.
• To support the preparation and hosting of competent authority inspections.
• To raise and support the investigation of deviations and associated CAPA’s.
• To support the collection of data for reporting Quality Assurance Performance Indicators.
• To support the implementation and management of stability programmes
• To perform any other appropriate duties at the request of the QC Head

Your Background:

• Ability to establish and maintain effective working relationships and communication links within affiliated organisations and other customers
• Extensive knowledge of Quality Control, Quality Assurance, Quality Systems, GMP, Regulatory Compliance and manufacture and packaging of pharmaceutical products
• Good technical and scientific judgement
• Ability to interpret complex data and present key findings
• Computer literate e.g. Word, Excel and PowerPoint
• Demonstrated Knowledge, understanding and application of GMP Guidelines and Regulations

Apply:


It is essential that applicants hold entitlement to work in the UK. Please quote job reference 134 138in all correspondence.