Supplier Quality Engineer

At Eakin Healthcare, we put patients at the heart of everything we do. We are a family-owned global medical device company with a proud heritage of innovation and care. We deliver innovative solutions across Ostomy, Respiratory, and Surgical therapies, along with our Respond home delivery service. Founded over 50 years ago, we now have a team of over 700 dedicated people across three UK manufacturing sites, 12 international sales and distribution centres and export to over 60 countries. We’ve been recognised as a Great Place to Work®! And we’re proud to be named among the Best Workplaces in Healthcare and Best Workplaces for Women.

At Eakin Healthcare, we’re united by one mission: working together to improve lives - just like we’ve been doing for over five decades.

WHY JOIN US?

We’re good at what we do – come and join us and you can benefit from:

Blended Working

Bonus

25 days holiday plus bank holidays (rising to 28)

Option to buy holiday days

Wellbeing Programme

Health Cash Plan

Pension

Life Assurance

Enhanced Maternity/Paternity

Cycle to Work Scheme

Referral Scheme

Long Service Awards

Free Parking

ABOUT THE ROLE

Reporting to the Supplier Quality Manager, the SQE will work closely with the Supplier base of the Eakin Healthcare Companies, striving for excellence in supplier quality performance and continuous improvement. SQE will ensure that Supplier Audits are conducted in line with agreed schedule, and Supplier Corrective Action Requests (SCAR) are raised and closed out accordingly and in line with QMS procedural requirements.

KEY ACTIVITIES

Create, implement and manage a risk-based Supplier Audit Schedule.

Schedule, organise, plan, conduct and report on all assigned Supplier Audits as per schedule, ensuring record keeping of all audit activities. This will include auditing both on site at supplier, and remotely.

Manage and co-ordinate the QMS SCAR processes, being the company contact point for such matters with both Internal Stakeholders and Suppliers.

Oversee and co-ordinate the proper completion, retention and review of supplier agreements, along with the relevant internal stakeholders.

Support innovation and new product introduction related to supplier selection and monitoring.

Provide input to the QA Monthly report, by providing line management with regular status updates and KPI measures.

Support the QARA Managers regarding the liaising with Notified Body and Competent Authority as required.

Collaborate with the introduction/function/improvement of the AQL sample inspection program for supplied components.

Support Internal audit program as required as both support and lead auditor.

Represent the Northern Ireland Businesses at all external agency and customer inspections.

Support the QA initiative to imbed a QA culture throughout the organisations.

Quality System

Maintain files and records in accordance with relevant QMS procedures and make them available for review during Quality Audits.

Support, where required, investigations into quality issues in manufacturing or customer complaints.

Comply with all applicable QMS processes at all times.

Health & Safety

Following all Health & Safety guidelines within the Department and notifying the Company of any incident, accident or near miss.

Other

To adhere to the company’s Equal Opportunities policy and Dignity at work policy in all activities and to actively promote equality of opportunity wherever possible

To be responsible for your own health and safety and that of your colleagues, in accordance with the company’s’ Health and Safety policy

To adhere to the company’s Quality policy and Environmental policy

To undertake other duties as may be reasonably required

KEY SKILLS

Essential

Previous experience of supplier management in a regulated industry - ideally Medical Device Manufacturing Company, with knowledge of ISO13485, MDSAP, EUMDR, EUMDD, UKCA & 21CFR820.

Experience of conducting / leading Supplier Quality Audits and internal audits

Strong command of written English

Excellent verbal communication skills

Excellent organisational and planning skills to deliver on a dynamic supplier audit schedule and completion of subsequent documentation.

Competent in the use of Microsoft office packages

Full driving license

Desirable

IRCA Approved Lead Assessor Qualified

Experience of problem-solving and risk management methodologies

Knowledge of and experience with CAPA process, including formal root cause analysis.

Experience of leading audits within a regulated or manufacturing environment

KEY WORKING RELATIONSHIPS

Internal

Quality & Regulatory, Operations and Supply Chain

External

Suppliers

Notified Bodies and Competent Authorities

Contractors

3rd party Clients

ADDITIONAL INFORMATION

Regular business travel required.

COMPETENCIES

Manages Complexity

Making sense of complex, high quantity, and sometimes contradictory information to effectively solve problems.

Decision Quality

Making good and timely decisions that keep the organization moving forward.

Plans and Aligns

Planning and prioritizing work to meet commitments aligned with organizational goals.

Ensures Accountability

Holding self and others accountable to meet commitments.

Collaborates

Building partnerships and working collaboratively with others to meet shared objectives.

Communicates Effectively

Developing and delivering multi-mode communications that convey a clear understanding of the unique needs of different audiences.

Persuades

Using compelling arguments to gain the support and commitment of others.

Being Resilient

Rebounding from setbacks and adversity when facing difficult situations.

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