Quality Engineer

Gold Group Ltd; Crawley; On-site; GBP 35,000 - 50,000; Full time

Job summary

A leading company in medical equipment manufacturing is seeking a Quality Engineer to support quality management systems and processes. The role involves collaboration with various teams, compliance activities, and promoting adherence to company values. Ideal candidates will have a degree in engineering and experience in quality assurance within a medical device environment.

Qualifications

• Experience in Quality, Regulatory, or Engineering roles within a medical device environment.
• Training in medical device regulatory standards.

Responsibilities

• Support local quality management system and processes.
• Prepare internal audit plans and execute audits.
• Analyze process data to drive optimization.

Skills

Communication

Problem-solving

Customer-focused

Education

Bachelor's degree in engineering

Job description

This range is provided by Gold Group Ltd. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.

Base pay range

Direct message the job poster from Gold Group Ltd

Job Title: Quality Engineer

As a Quality Engineer, you will support the local quality management system and processes. You will act as an advocate of Quality and promote the group's vision and mission while supporting the goals of the overall business. You will work closely with functional teams in areas such as Supplier Quality, Manufacturing, Order Fulfillment, and Regulatory Affairs.

Responsibilities

1. Work on projects and compliance activities to completion.
2. Prepare monthly metrics for your area of responsibility.
3. Analyze process data and trends to drive optimization and improvement.
4. Represent the QA organization in specific processes (e.g., CAPA, Order Fulfillment, Manufacturing, Deviation Management).
5. Support other members of the QA organization and other functions on technical aspects to achieve results.
6. Participate in external audits by regulatory authorities.
7. Promote and maintain adherence to company values.
8. Prepare internal audit plans, execute audits, and draft audit reports as applicable.

Required Skills and Experience

1. Bachelor's degree in engineering or a related field, or a formal engineering apprenticeship with relevant experience.
2. Training and experience in relevant medical device regulatory standards (e.g., ISO, IEC, MDR, MDSAP).
3. Lead auditor training in ISO 13485/9001.
4. Proven experience in Quality, Regulatory, or Engineering roles within a medical device environment.
5. Strong communication skills, both written and verbal, with the ability to collaborate effectively.
6. Objective-driven and customer-focused.
7. Ability to work independently and produce results.
8. Professional integrity and ability to translate regulations into business requirements.
9. Structured problem-solving skills with knowledge of quality tools and techniques.

Additional Information

Services advertised by Gold Group are those of an Agency and/or an Employment Business. We will contact you within 14 days if selected for an interview. For our privacy policy, please visit our website.

Job Details

• Seniority level: Mid-Senior level
• Employment type: Full-time
• Industry: Medical Equipment Manufacturing

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