Manufacturing Tooling Specialist
hace 5 días
Horizons is a leading US-based medical technology company seeking a dynamic Manufacturing Engineer to join its team as an Injection Molding Tooling specialist. The role offers an exciting opportunity to work on cutting-edge projects that make a real impact in healthcare.
Job OverviewThis key position will lead site and project-based manufacturing activities to implement, qualify, and sustain electro-mechanical products. As a Manufacturing Tooling Specialist, you'll be responsible for managing tool assets, optimising processes, and ensuring the highest quality standards.
Responsibilities- Tool Management: Collaborate with contract manufacturers to design, implement, and validate injection molding tools and processes, ensuring compliance with product specifications and quality criteria.
- Production Support: Ensure the ongoing manufacture of high-quality products while meeting safety, quality, cost, and delivery targets for first and second-tier suppliers.
- Continuous Improvement: Drive process enhancements to meet the company's improvement goals, focusing on tooling, polymer manufacturing, and metrology.
- Cost Optimization: Implement design iterations to reduce costs while enhancing patient safety for BD products.
- Documentation Management: Maintain configuration management of engineering change documentation in line with quality management system requirements.
- Cross-Functional Collaboration: Engage with various teams to ensure compliant execution of quality systems and processes.
- Global Travel: Be prepared to travel internationally to manage tool trials and process development.
To succeed in this role, you'll need:
- Experience HNC, HND, or Degree in Engineering (or equivalent).
- 3+ years of experience in injection molding and tooling, ideally with medium-volume products.
- Proficiency in electro-mechanical assembly, machining, and plastic injection molding.
- Knowledge of scientific molding techniques and production line quality control.
- Experience in regulated environments, preferably in medical devices.
- Strong communication skills, both verbal and written, including technical writing.
- Familiarity with validation processes (TMV, IQ, OQ, PQ) and quality systems (cGMP, CFR820, ISO13485).
- Demonstrated problem-solving abilities and project management skills.
$80,000 - $110,000 per annum, depending on experience.
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