Quality & Compliance Engineer

Rise Technical Recruitment Ltd; Houghton-le-Spring; Presencial; GBP 37.000 - 40.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Training

Holidays

Enhanced Pension

Descripción de la vacante

Rise Technical Recruitment Ltd in the North East is seeking a Quality & Compliance Engineer on a 12-14 month fixed term contract. You will support quality and regulatory requirements across design, manufacture and testing in a medical device environment.

The role covers CAPA, data analysis, audits, inspections, and maintaining quality systems (ISO 13485/EU MDR). You will join a globally recognised manufacturer, with excellent training, holidays and a strong pension.

Formación

• Experience in medical device quality systems and regulatory activities.
• Evidence of applying EU MDR and ISO 13485 knowledge.
• Bachelor's degree in Engineering, Life Sciences, or related field.
• Ability to support CAPA investigations and audits.

Responsabilidades

• Support quality and regulatory requirements across design, manufacture and testing.
• Maintain quality procedures, analyse data and manage CAPA activities.
• Support medical device inspections, audits and clean-room production.
• 12-14 month maternity cover contract.
• 8am - 4pm Monday to Friday.

Conocimientos

Quality engineering

Regulatory compliance

CAPA management

Educación

Engineering, Life Sciences or related degree

Herramientas

ISO 13485

EU MDR

Descripción del empleo

Quality & Compliance Engineer

£37,000 - £40,000 + 12-14 Month Fixed Term Contract + Excellent Training + Holidays + Enhanced Pension + Monday-Friday + Great Benefits Package

Houghton Le Spring (Commutable from Sunderland, Newcastle, Washington, Gateshead, Hartlepool, Newton Aycliffe, Billingham, Peterlee, Consett, South Shields)

Are you a Quality or Regulatory Engineer with experience in medical devices, looking for a varied fixed term contract within a specialist manufacturing environment?

This is a fantastic opportunity to play a key role across product quality and regulatory compliance, supporting projects from design and development through to manufacture, testing and release.

The company are a long-standing, globally recognised manufacturer with an excellent reputation in their industry. Due to maternity cover, they are now looking for an experienced quality professional to join their team on a 12-14 month fixed term contract.

Within the role, you will develop and maintain robust quality processes, support production teams, review performance data and investigate non-conformances to establish effective corrective and preventive actions. You will also inspect and evaluate medical devices, assist with regulatory activities and audits, and help ensure clean-room production continues to meet the required standards.

This position would suit a Quality or Regulatory Engineer with experience of medical device quality systems who is looking to make an immediate impact within a stable, forward-thinking manufacturer.

The Role:

• Support quality and regulatory requirements across design, manufacture and testing
• Maintain quality procedures, analyse data and manage CAPA activities
• Support medical device inspections, audits and clean-room production
• 12-14 month maternity cover contract
• 8am - 4pm Monday to Friday

The Person:

• Quality, Regulatory or Quality Assurance Engineer
• Engineering, Life Sciences or related degree
• Medical device regulatory or quality systems experience
• EU MDR, ISO 13485 or technical documentation experience advantageous

Quality, Regulatory, Compliance, Medical Device, Audit, Manufacturing, Engineering, Life Sciences

Reference Number: BBBH281453

We are an equal opportunities company and welcome applications from all suitable candidates.