Back to Job SearchROLE OVERVIEW
An exciting opportunity for a Quality Engineer to join a leading medical device company operating within the regulated life sciences industry. This fully remote role offers flexibility and the chance to work on a high-impact remediation project that focuses on enhancing quality standards across multiple stages of product development and manufacturing. Our client is seeking a dedicated professional to ensure compliance and continuous improvement in their quality assurance processes.
As a vital member of the team, the Quality Engineer will play a key role in maintaining rigorous quality systems, supporting project execution, and driving corrective and preventive actions to uphold the highest standards of safety and effectiveness.
KEY DUTIES AND RESPONSIBILITIES
Your duties as the Quality Engineer will be varied; however, the key duties and responsibilities are as follows:
• To design, implement, and maintain quality assurance protocols for materials, partially finished, and finished products, ensuring compliance with industry standards.
• Lead and execute moderate to complex projects, including Change Orders (ECOs), CAPAs, Non-Conformance Events (NCE), and product/process investigations.
• Write, execute, and coach others on PQs, TMVs, and simple procedure updates, ensuring team adherence to quality standards.
• Perform risk management, defect investigations, and root cause analyses, providing sustainable corrective actions and preventive measures.
• As the Quality Engineer, you will support continuous improvement initiatives and contribute to high-level remediation efforts within a regulated environment.
ROLE REQUIREMENTS
To be successful in your application to this exciting role as the Quality Engineer, we are looking to identify the following on your profile and past history:
• A Degree or higher level in a technical/scientific discipline; a Master’s or PhD experience is beneficial.
• Proven industry experience in Quality Systems within regulated industries, preferably medical devices.
• A working knowledge and practical experience with GMP, GLP, ISO, Six Sigma, Root Cause Analysis, and statistical analysis.
WHAT’S IN IT FOR YOU?
- Competitive remote working setup, offering flexibility to work from anywhere.
- Opportunity to contribute to a high-impact remediation project within the medical device sector.
- Join a forward-thinking organization committed to quality and continuous improvement.
- Develop your expertise in regulated environments with leading industry professionals.
Key Words: Quality Engineer / Medical Device / Remediation Project / Fully Remote / Quality Assurance / CAPA / Risk Management / Root Cause Analysis / GMP / ISO
"Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer. We welcome applications from anyone who meets the role requirements. HRS exclusively supports the STEM sectors, combining recruitment expertise with scientific knowledge to help you advance your career."
Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer. We welcome applications from anyone who meets the role requirements. HRS exclusively supports the STEM sectors, combining recruitment expertise with scientific knowledge to help you advance your career.
