Senior Quality Systems Specialist

Stryker Group; Belfast; On-site; GBP 45,000 - 60,000; Full time

Job summary

A global medical device company is seeking a Senior Quality Systems Specialist in Belfast to lead quality system improvement projects and ensure regulatory compliance with FDA and ISO standards. The ideal candidate will have a Level 6 qualification in a relevant field and at least 3 years of experience in a manufacturing environment. Strong skills in project management, technical writing, and effective communication are essential for success in this role, making a significant impact on quality systems across the organization.

Qualifications

• Minimum of 3 years experience in manufacturing environment or equivalent preferred.
• Understanding of FDA 21 CFR Part 820, ISO 13485, and ISO 14971.

Responsibilities

• Lead quality system improvement projects based on internal assessments.
• Map and analyze quality processes to identify improvement priorities.
• Collaborate across departments to implement quality improvements.
• Support audits by providing complete and accurate documentation.

Skills

Experience in regulated environment and interaction with regulatory agencies

Strong knowledge of Quality Systems (CAPA, audits, etc.)

Excellent technical writing and documentation skills

Strong communication and project management skills

Analytical and problem-solving capabilities

Ability to plan, organize, and implement multiple tasks

Education

Level 6 qualification in Science, Engineering, Business or related discipline

Tools

Microsoft Office

MS Project

Adobe Acrobat

Job description

Join our team in Belfast as a Senior Quality Systems Specialist

Position Summary

The Senior Quality Systems Specialist is responsible for leading and executing quality system improvement activities to ensure compliance with FDA 21 CFR Part 820, ISO 13485, and other applicable global medical device regulations. This role focuses on evaluating, harmonizing, and improving existing quality system processes, documentation, and controls to address opportunities for improvement identified through internal assessments and audits.

Key Areas of Responsibility

• Lead improvement projects related to quality system opportunities identified through internal assessments and audits.
• Map and gap-analyze existing quality processes (CAPA, Complaints, Design Controls, Document Control, etc.) to identify improvement priorities.
• Assess and revise quality procedures, work instructions, and forms to ensure alignment with regulatory requirements and corporate requirements, ensuring alignment with the organization’s quality system harmonization strategy.
• Identify, initiate and own Nonconformances to address systemic compliance issues.
• Partner cross-functionally with Manufacturing, R&D, Quality and Regulatory to implement sustainable quality improvements.
• Support verification of quality system changes, ensuring effective implementation and ongoing compliance.
• Facilitate document change review and approval through electronic document management system.
• Collaborate with Training Team to establish training on revised quality system procedures and compliance expectations.
• Track and report progress, key metrics, and issues related to quality system harmonization and improvements.
• Ensure continued and effective communication with project management and stakeholders of key decisions, risks and roadblocks.
• Ensure ongoing compliance with FDA, ISO 13485, MDSAP, and EU MDR throughout integration efforts.
• Support internal and external audits by providing documentation and ensuring records are complete, accurate, and retrievable.

• Perform other related duties as assigned

Qualifications

• Level 6 qualification required, preferably in a Science, Engineering, Business or related discipline.
• Minimum of 3 years experience in manufacturing environment or equivalent preferred.

Knowledge

• Experience in regulated environment and interaction with regulatory agencies
• Understanding of FDA 21 CFR Part 820, ISO 13485, and ISO 14971.
• Strong knowledge of Quality Systems (CAPA, audits, Management Review, Quality Planning, etc.)
• Excellent technical writing and documentation skills.
• Strong communication, project management and influencing skills.
• Ability to plan, organize, and implement multiple concurrent tasks.
• Strong interpersonal skills, written, oral communication and negotiations skills. Must demonstrate the ability to effectively communicate up/down and across different levels of the organization.
• Analytical and problem-solving capabilities with the ability to draw insights from data quickly and to define executable actions.
• Demonstrated ability to work in cross-functional team environments.
• Experience in compliance risk situations.

System/Computer Requirements:

• Basic Microsoft Office, MS Project, Adobe Acrobat