Senior Engineer, Advanced Operations

Work Flexibility: Hybrid or Onsite 23 month fixed term contract All benefits included Hybrid, Carrigtwohill, Cork

Join Our Team as a Senior Engineer, Advanced Operations

Are you an experienced and innovative engineering professional with a passion for advancing cutting-edge technologies in the medical field? We are looking for a proactive, results-driven Senior Engineer to support our NPI programs working on our Patient Specific Joint Replacement portfolio. In this role, you will develop solutions to technical challenges of moderate scope and complexity, while playing a key part in leveraging engineering techniques to ensure NPI launch excellence. You will also lead continuous improvement initiatives aimed at accelerating time to market, driving cost efficiencies, and expanding margins by implementing innovative additive technologies and processes that differentiate our products and give us a competitive edge in the market.

Key Responsibilities

• Innovative Technology Integration: Support the integration of cutting-edge additive manufacturing technologies for joint replacement products, optimizing efficiency and precision in accordance with Stryker's new product development and design transfer procedures.
• Relationship Building and Mentorship: Foster productive relationships both internally and externally, playing a pivotal role in team dynamics. Provide periodic guidance and training to team members, contributing to a culture of continuous learning and growth.
• Quality Assurance and Product Optimization: Oversee and ensure the quality of processes and products, aligning with operational standards and material specifications to deliver superior joint replacement products.
• Collaborative Project Management: Collaborate closely with cross-functional teams to ensure seamless coordination and synergy in all aspects of the product development lifecycle.
• Analytical Expertise: Analyze equipment to establish operating data, conduct experimental tests, and review results. You may also lead or act as an independent reviewer in process review meetings.
• Regulatory Compliance and Time Management: Ensure adherence to regulatory requirements while effectively managing project deadlines and product costs to facilitate swift market delivery.
• Participate in Equipment Qualifications, PFMEA, Control Plan, SOP, and PPAP generation associated with design transfer and product launches.

Qualifications and Skillsets

• B.S. in Mechanical Engineering or related discipline with 2+ years of experience or a related Master's degree.
• Excellent Interpersonal skills - able to express ideas and collaborate effectively with multidisciplinary teams.
• Innovative mindset with the ability to envision novel approaches to problem-solving and process improvement.
• Experience in executing complex problem solving techniques related to manufacturing/design technical issues.
• Good instincts and sound judgement for mechanical and structural design.
• Good understanding of Design for Manufacturing (DFM), statistical tools, and validation/verification techniques.
• Experience in CAD platform development and have the ability to streamline design processes and ensure seamless integration with complex engineering workflows preferred.
• Good knowledge of manufacturing processes, product/process design, and engineering materials.
• Experience in an FDA regulated or regulated industry is beneficial.

Join our team, and become an integral part of a transformative initiative that aims to redefine the landscape of joint replacement products. Be prepared to contribute your expertise and vision to a team that values innovation, collaboration, and the pursuit of excellence in engineering. Exciting challenges await you!

Pay Ranges

Ireland: €47,000 - €77,000 EUR Annual

Travel Percentage

10%

Work Flexibility Details

Remote - Role allows you to work the majority to 100% of time from an alternate workplace. These roles could have travel expectations, and you must work within the country of the job requisition location.

Field-based - You can expect to regularly work a majority to 100% of time at customer facilities and has a set territory or expectation to travel within a set boundary. Almost all sales roles would likely be qualified as field-based.

Onsite - Role is 100% located at a Stryker facility. Some ad hoc flexibility may be available depending on role, level, and job requirements. Manufacturing roles and any role that requires physical presence at the office would qualify under this category.

Hybrid - You can expect to regularly work in both an alternate workplace and a Stryker facility. Roles that are partially remote or co-located would qualify as hybrid, and the expectation to be onsite would be defined and agreed upon by your manager/supervisor.

Stryker is one of the worlds leading medical technology companies and, together with its customers, is driven to make healthcare better. We offer innovative products and services in Orthopaedics, Medical and Surgical, and Neurotechnology and Spine that help improve patient and hospital outcomes. We are proud to be named one of the World's Best Workplaces! For more information, visit: