Quality & Compliance Engineer

Rise Technical Recruitment Limited; Houghton-le-Spring; On-site; GBP 37,000 - 40,000; Full time

Benefits offered by this job

Excellent Training

Holidays

Enhanced Pension

Great Benefits Package

Job summary

Rise Technical Recruitment Limited is seeking a Quality & Compliance Engineer for a 12-14 month fixed-term contract at a Houghton Le Spring site in England. The role covers design, manufacture and testing, ensuring quality and regulatory compliance for medical devices.

You will develop and maintain quality processes, review performance data, investigate non-conformances and support audits; experience with EU MDR and ISO 13485 is advantageous.

Qualifications

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

Responsibilities

• 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.

Skills

Quality Engineering

Regulatory Engineering

Quality Assurance

CAPA Management

Education

Engineering Degree

Life Sciences Degree

Related Field

Tools

EU MDR

ISO 13485

Job description

Quality & Compliance Engineer (BBBH281453) Houghton Le Spring, England

Salary: GBP37000 - GBP40000 per annum + Great Benefits Package

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