Qa Validation Engineer

The QA Validation Engineer is responsible for coordinating, implementing, and maintaining the site validation program to ensure compliance with external regulatory requirements and industry best practices.

The role involves oversight of validation activities for equipment, utilities, processes, and software, as well as participation in broader Quality Assurance initiatives.

KEY RESPONSIBILITIES

Validation & Quality Assurance

Coordinate, direct, and actively participate in validation and QA activities for site equipment, utilities, processes, and software.

Ensure compliance with FDA, European cGMP, and GAMP standards.

Develop, maintain, and execute the Site Validation Master Plan and Project Validation Plans.

Generate validation protocols, reports, and investigations to meet cGMP standards.

Implement corrective actions as identified through validation investigations.

Documentation & Compliance

Create, review, and approve quality documents and test data.

Manage validation, exception events, and change control processes.

Maintain validation equipment records and ensure accurate tracking.

Document all activities per cGMP requirements and update procedures to reflect current best practices.

Training & Continuous Improvement

Complete all required training before performing tasks.

Cross-train within the team and support onboarding of new team members.

Participate in continuous improvement initiatives across manufacturing, quality, safety, and training systems.

Communication & Team Collaboration

Coordinate team activities for maximum efficiency.

Maintain overall cGMP compliance in production areas.

Communicate effectively with peers and management, escalating issues as needed.

REQUIREMENTS

Essential Qualifications

Qualification and / or degree in engineering or a scientific discipline.

Experience & Skills

3+ years of validation or quality experience in medical device plastics processing, moulding, or assembly operations.

3+ years of knowledge in cGMP and regulatory requirements for the medical device industry.

Strong communication (written and oral), presentation, and troubleshooting skills.

Effective interpersonal and organizational skills.

Ability to work independently and collaboratively in a team environment.

Strong prioritization and multitasking abilities.

Cognitive Skills

Ability to identify systems and processes requiring validation or QA support, ensuring timely documentation and resolution.

Strong communication and motivation skills.

Apply today!

Our Vision : To be recognised as the best STEM Contracting & Permanent Recruitment company and the Employer of Choice for top performing Recruiters

For further information on this role please contact Róisín Vaughan on /

Check out all our open jobs on our HERO Recruitment website - HERO Recruitment : Leading STEM Recruitment Agency

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