Work Your Magic with us!
Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich people’s lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us.
The Role
Reporting to the Senior Engineer, the Process Engineer is primarily responsible for supporting day-to-day production in one or more of the manufacturing areas and effectively implementing change management projects.
Duties include
- Provide day-day Technical support for processing issue or changes on existing manufacturing processes. Lead and coordinate the troubleshooting of various manufacturing process issues.
- Initiate, co-ordinate and complete assigned projects within the Process and Technology group supporting manufacturing. Using a structured approach and detailed planning to deliver projects that meet or exceed stakeholder expectations and that are delivered Right First Time, Safely, on schedule and within budget.
- Maintain and develop manufacturing process documentation and procedures. All process changes and modifications to be documented and tracked closely.
- Complete Process / Product Validations within the department as they arise, in conjunction with Quality/Validation group.
- Lead and coordinate the execution of OQ / PQ builds. Preparing protocols for process / material changes as needed. Liaising with operations and technician group to prepare plan for validation builds. Execute builds supporting any process adjustments and Compile OQ / PQ validation reports and deviations as required.
- Thorough investigation of Manufacturing, Quality and EHS issues using Root Cause Analysis methodology, and implementation of robust corrective and preventative actions to prevent recurrence.
Who You Are
Education: Degree in Mechanical / Process Engineering or equivalent years of experience.
Experience: 3+ years relevant experience, preferably within Medical Device industry or other regulated environments.
Working knowledge of Product & Process validations essential.
Excellent engineering ability
Strong organisational ability
Self motivation and drive
Team Orientated
Demonstrate a high level of responsiveness to internal customers (eg. production)
Communication- strong written, oral and presentational skills.
Working Knowledge of the following would be an advantage but not a requirement;
- Automated / Semi Automated assembly equipment.
- Injection moulding and mould tools.
- High precision Punch & Die Sets.
- Heat sealing, ultrasonic welding, leak testing, vision systems.
- OEE Line performance methodology.
- Minitab/ Lean 6 Sigma techniques
- Root Cause Analysis methodology
- Microsoft Excel to an advanced level
AutoCAD.
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What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We celebrate all dimensions of diversity and believe that it drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress!
Apply now and become a part of our diverse team!
