Project Engineer, Manufacturing at Stryker - New Zealand

Limerick, Munster, Ireland -

Full Time

Start Date

Immediate

Expiry Date

12 Jul, 26

Salary

0.0

Posted On

13 Apr, 26

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

CNC machining, Metrology, Packaging, Biomaterial production, Coatings, Validation, IQ, OQ, PQ, PFMEA, Control plans, Good manufacturing practices, MSA studies, Project engineering, Mechanical engineering, Technical documentation

Industry

Medical Equipment Manufacturing

Description

Work Flexibility: Not available Project Engineer, Manufacturing Position Summary The Project Engineer will provide technical support under supervision across various project-related activities. Knowledge of the design, development, and validation of manufacturing technologies is essential for the role, particularly in one or more of the following areas: CNC machining, metrology, packaging, biomaterial production, and coatings. This role will assess and implement equipment and process changes to the current manufacturing lines, ensuring compliance of Stryker’s products with relevant regulatory requirements and medical device standards. Key Areas of Responsibility Under supervision, provide engineering support for new equipment and process changes, ensuring that all activities are completed and documented in accordance with regulatory requirements. Under supervision, technically support the introduction of new capital equipment and support the associated qualification and validation activities - VP, IQ, OQ, PQ. Assist with testing for validations where required. Under supervision, evaluate process layouts to support new process integration while ensuring optimal utilisation of floor space and optimum process flow. Development and implementation of appropriate supporting documentation, SOPs, PFMEA, Control Plans and process work instructions compliant with current Good Manufacturing Practices (GMP). Under supervision, transferring and implementing processes, either from development or from another manufacturing facility. Support budgetary, scheduling, and project databases, and report regularly to the project manager on progress as well as on problems that could significantly affect cost or schedule. Under supervision, developing specifications in the form of a URS for new equipment purchases. Under supervision, support capital acquisition activities. Under supervision, conduct MSA studies for products and new processes. Responsibility as technical support for projects (value stream and cross-functional) as assigned by the company, including the scoping, approval, budgeting, specification, execution, qualification and operational handover as appropriate. Observing the Quality Management Systems requirements on site at all times. Demonstrate ownership and integrity of work. Provision of out-of-hours support to the business as required by management or as mandated by shutdowns and/or equipment failures. All other duties as assigned. Qualifications Knowledge Skills Level 8 Degree in Mechanical Engineering or equivalent technical experience is required. Proven Project Engineering skills through the delivery of business-critical projects. 0+ years of work experience. Strong communication and influencing skills with both internal and external agents. Under supervision capable of technical leading, influencing and providing technical direction to Co-op Students, Technicians and operators as required. Capable of working as part of a multi-disciplined team in an aggressive, dynamic and results-oriented environment. Demonstrable analytical & problem-solving skills, a process improvement orientation, and the ability to handle multiple tasks in a fast-paced and results-oriented environment. Technological pioneer, willing to source, investigate and implement technological and automation advances. Confident and effective decision maker, with a proven leadership ability to negotiate and influence others. Travel Percentage: None Stryker is one of the world’s 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: www.stryker.com Work Flexibility 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.

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Responsibilities

The Project Engineer provides technical support for manufacturing equipment and process changes, ensuring compliance with regulatory requirements and medical device standards. They are responsible for supporting capital acquisition, validation activities, and the implementation of process improvements within the manufacturing facility.