Supplier Quality Engineer

Join Our Team as a Supplier Quality Specialist in the 24 Month Contract role 

Are you passionate about quality systems and supplier management? Do you thrive in a collaborative environment and have a keen eye for detail? If so, we have an exciting opportunity for you

Summary:
This role will mean you will join a dynamic and inclusive team that values collaboration and innovation. The Supplier Quality Engineer will contribute to meaningful projects that impact the quality and safety of medical devices and provides a great opportunity to grow your career in a supportive environment that encourages continuous learning and development.

Responsibilities:

• Lead and support all aspects of Quality Systems related to supplier quality, including procedures, risk assessment, and maintaining the Approved Supplier List (ASL) and Supplier Qualification Plan.
• Collaborate with corporate supplier quality teams on various projects.
• Administer and execute the supplier quality system (QSA) as per the schedule
• Actively participate in the On Body Injector (OBI) mock audit team.
• Prepare and maintain supplier-related documentation (Product Quality Assessment, Certificate of Conformance) in compliance with regulatory requirements.
• Support projects to qualify new or alternative suppliers or materials and drive continuous improvement activities.
• Lead material investigations raised by Notification of Event (NOE) or Quality Notification (QN) with suppliers and conduct effectiveness checks.
• Manage all quality-related aspects of materials used to make delivery devices and suppliers of those materials. This includes managing and executing supplier audits, incoming inspections, non-conformance investigations, supplier monitoring, and communication.
• Support supplier process validation, materials/supplier change project management, and supply chain efficiency improvement.

Educational Requirements:

• A primary degree in Science or Engineering Discipline.

Relevant Experience:

• Minimum of 3 years of relevant work experience in an ISO9001 or ISO13485 environment, preferably within the medical devices or pharmaceutical industry.
• Experience in preparing technical documentation.
• Proven ability to work effectively in a cross-functional team environment.
• Excellent interpersonal and communication skills.
• High level of computer literacy.
• Experience in statistical analytical skills.

This role will be a hybrid working role 
Apply now and join our team of dedicated professionals

embecta is an Equal Opportunity/Affirmative Action Employer.  We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status.