QC Analyst, Serology (GMP) – Flexible Benefits

AliveDx; United Kingdom; Teletrabalho; GBP 32 000 - 42 000; Tempo integral

Vantagens oferecidas por esta oferta de emprego

Private medical cover

Life assurance

Additional annual leave

Cycle to work

Marketplace discounts

Resumo da oferta

AliveDx in the United Kingdom is seeking a Quality Control Analyst to join the QC Serology Department at the ARC facility near Edinburgh. The role focuses on GMP-compliant QC testing of raw materials, intermediates and final products to ensure regulatory release to market.

You will work 37.5 hours per week in a full-time, permanent position, performing test procedures, recording data, and contributing to continuous improvement initiatives while upholding safety and quality standards.

Qualificações

• Experience working in a GMP environment.
• Ability to follow SOPs and GMP requirements.
• Strong attention to detail and accuracy.
• Capacity to work under pressure and meet timelines.

Responsabilidades

• Conduct GMP-compliant quality control testing of raw materials, intermediates, and final products.
• Execute test procedures per SOPs and regulatory policies.
• Record data in batch records ensuring traceable documentation.
• Participate in routine QC testing of Serological products.
• Prepare reports as required.
• Assist training of staff to develop capabilities.
• Monitor equipment operation and maintenance for safety.
• Participate in projects to drive continuous improvement.

Conhecimentos

GMP experience

Laboratory testing

Quality control mindset

Data recording & reporting

Descrição da oferta de emprego

AliveDx in the United Kingdom is seeking a Quality Control Analyst to join the QC Serology Department at the ARC facility near Edinburgh. The role focuses on GMP-compliant QC testing of raw materials, intermediates and final products to ensure regulatory release to market.

You will work 37.5 hours per week in a full-time, permanent position, performing test procedures, recording data, and contributing to continuous improvement initiatives while upholding safety and quality standards.