Find Pharmaceutical manufacturing Jobs in Ennis County Clare

Graduate Quality Engineer
Zimmer Biomet —Shannon, County Clare
- Full-time
- Engineering
- Microsoft Office
- Manufacturing
- Wellness program

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Graduate Quality Engineer

Zimmer Biomet -
Shannon, County Clare

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Job details

Full-time

Benefits

Wellness program

Qualifications

Engineering
Microsoft Office
Data collection
Manufacturing
Communication skills

Full job description

At Zimmer Biomet, we believe in pushing the boundaries of innovation and driving our mission forward. As a global medical technology leader for nearly 100 years, a patient’s mobility is enhanced by a Zimmer Biomet product or technology every 8 seconds.

As a Zimmer Biomet team member, you will share in our commitment to providing mobility and renewed life to people around the world. To support our talent team, we focus on development opportunities, robust employee resource groups (ERGs), a flexible working environment, location specific competitive total rewards, wellness incentives and a culture of recognition and performance awards. We are committed to creating an environment where every team member feels included, respected, empowered and recognised.

What You Can Expect

The Graduate Quality Engineer is a structured 24-month development role designed to build core capability in quality engineering, quality systems and cross-functional project support within Zimmer Biomet. The role holder will be based in Shannon for 18 months and will complete a 6- month rotation in the Galway site to gain wider operational exposure. Through coached assignments and formal training, the graduate will develop practical knowledge of manufacturing quality, non-conformance management, CAPA, internal and external risk management, audit readiness and project execution while supporting compliance with applicable quality and regulatory requirements.

How You'll Create Impact

Support quality engineering and quality systems activities to help ensure products and processes conform to established requirements and standards.
Assist with the development, review and maintenance of procedures, specifications, forms and quality records in line with site requirements.
Participate in investigations relating to non-conformances, quality issues, complaints or process deviations and support timely follow-through of resulting actions.
Support CAPA activities, including problem definition, root-cause analysis, action tracking, effectiveness review and closure support.
Assist with risk management activities for both internal and external issues, including participation in risk assessments and updates to associated documentation as required.
Support validation, inspection planning, data collection and trending activities to help monitor process and product quality performance.
Compile, analyse and present quality data to support decision-making, continuous improvement and project reporting.
Contribute to audit preparation and follow-up activities and, as capability develops, participate in internal audit activities under guidance.
Work with cross-functional teams including Manufacturing, Operations, Supply Chain and other support functions on quality-related projects and improvement initiatives.
Complete the planned Shannon-to-Galway site rotation and apply learnings across both site environments.
Maintain training compliance and complete the structured development plan associated with the graduate programme.
Perform other quality-related duties consistent with the level and developmental nature of the role.

What Makes You Stand Out

Strong interpersonal, communication and learning agility skills.
Demonstrated interest in quality, compliance, manufacturing or regulated industry environments.
Good analytical and problem-solving capability, with attention to detail and a structured approach to work.
Ability to work effectively in a team environment and build relationships across functions and sites.
Working knowledge of Microsoft Office applications.
Willingness to learn quality system requirements, audit principles, CAPA methodology and risk management tools.
Ability to organise work, manage deadlines and respond positively to coaching and feedback.

Your Background

Recent graduate, or expected to graduate before programme start, with a third-level qualification in Quality, Engineering, Science or a related discipline.
Relevant placement, internship, project or academic experience in a manufacturing, medical device, pharmaceutical or other regulated environment would be advantageous but is not essential.
Demonstrated motivation to pursue a career in quality engineering within a regulated industry environment.

Travel Expectations

Occasional inter-site travel as required for training and project support

EOE/M/F/Vet/Disability

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