QC Analyst

TieTalent; Hatfield; On-site; GBP 30,000 - 40,000; Full time

Job summary

Un leader mondial dans le secteur pharmaceutique, basé à Hatfield, recherche un QC Analyst pour un contrat de 1 an. Le candidat idéal sera responsable des tests de matériaux, de la calibration des équipements et du respect des systèmes de qualité. Ce rôle nécessite des compétences solides en contrôle qualité, conformité réglementaire, et une capacité à travailler efficacement dans un environnement dynamique.

Qualifications

• Connaissance approfondie du contrôle de la qualité, GMP, et conformité réglementaire.
• Capacité à interpréter des données complexes et présenter des résultats clés.
• Excellentes compétences en communication et relations de travail efficaces.

Responsibilities

• Tester tous les matériaux selon les spécifications et procédures.
• Maintenir les systèmes de qualité et soutenir les audits internes et externes.
• Écrire des SOPs liées au support QC sous supervision.

Skills

Quality Control

Quality Assurance

GMP

Regulatory Compliance

Technical Judgment

Data Interpretation

Tools

Word

Excel

PowerPoint

Job description

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About

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

Key Duties Will Include

• Testing all materials according to specifications and procedures.
• Qualifying and calibrating laboratory equipment.
• Maintaining laboratory and Quality Systems in compliance with procedures.
• Writing SOPs related to QC support under supervision.
• Supporting internal and external audits, including inspections.
• Investigating deviations and supporting CAPA processes.
• Collecting data for Quality Assurance Performance Indicators.
• Supporting the implementation of stability programmes.
• Performing other duties as requested by the QC Head.

Candidate Background

• Ability to establish effective working relationships and communication links within organizations.
• Extensive knowledge of Quality Control, Quality Assurance, GMP, Regulatory Compliance, and pharmaceutical manufacturing and packaging.
• Good technical and scientific judgment.
• Ability to interpret complex data and present key findings.
• Computer literacy in Word, Excel, PowerPoint.
• Understanding and application of GMP guidelines and regulations.

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

Nice-to-have Skills

• Quality Control
• PowerPoint

Work Experience

• Quality Assurance (QA)

Languages

• English

Seniority Level

• Entry level

Employment Type

• Full-time

Job Function

• Quality Assurance

Industries

• Technology, Information and Internet