Campus Pride Jobs

We are excited to be named one of the World’s Best Workplaces by Fortune Magazine!

We are proud to offer you our total rewards package which includes bonuses, healthcare, insurance benefits, retirement programs, wellness programs, as well as service and performance awards – not to mention various social and recreational activities, all of which are location specific.

Responsibilities

• Ensure all solutions meet critical design prerequisites including patient and customer safety, mechanical, and biological suitability;

• Read and work from various clinical imaging including x-rays, CT, and MRI scans

• Preparation of surgical planning guides/instructions inclusive of appropriate surgical instruments and defining operating instructions for patient-specific implants;

• Liaise with Design coordinators, Manufacturing Team Leaders and technicians, Product Engineers, Inspectors, Customer Services, QA/RA personnel, and subcontractors with respect to the manufacture and progress of each case;

• Liaise with consultant surgeons, surgical/theatre staff, distributors, and the Sales team with respect to implant design, instrumentation and technical support;

• Ensure all patient-specific designs are covered by an appropriate Technical File/Design Dossier/Device History File;

• Conduct, as part of a team, risk assessments and document all activities and justifications/validations to satisfy regulatory requirements under the guidance of the Quality and Regulatory Affairs counterparts;

• Attend surgical and clinical cases, both domestic and abroad as required.

• Any other tasks that sits outside your current role from time to time to support the activities of the business.

Skills & Experience -

• Minimum of Bachelor’s degree in a science, engineering or related discipline. Mechanical or Biomedical Engineering preferred. Advanced degree in a technical discipline preferred.

• 2-3 years’ experience in medical device industry preferred, Overall, 5-8 years’ experience preferred.

• Good understanding of Creo, Materialise Mimics - segmentations of bone models, understanding CT scan , Anatomy of Hip & knee joints will be preferred.

• Can use CAD to a high level to design 3D parametric models and assemblies using Creo taking into consideration manufacturing and inspection routes.

• Able to interprete Voice of customer and draft design controls in compliance to ISO 13485, ISO 14971.

• Draft, tolerance and apply GD&T correctly and precisely

• Can support various departments, including manufacturing and inspection, regulatory and other functions and maintain strict document control.

• Can manage and schedule multiple projects both short and long term and keep to strict deadlines in a methodical manor.

• Self-motivation and focus to work individually or in small team environments.

• An eye for creative/innovative design and attention to detail.

• Understanding of biomedical and biomechanical engineering, bio tribology, or biomaterials.

Stryker is a global leader in medical technologies and, together with its customers, is driven to make healthcare better. The company offers innovative products and services in MedSurg, Neurotechnology, Orthopaedics and Spine that help improve patient and healthcare outcomes. Alongside its customers around the world, Stryker impacts more than 150 million patients annually.

Stryker Corporation is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, or protected veteran status. Stryker is an EO employer – M/F/Veteran/Disability.