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Key Responsibilities:
Participates in and leads projects to drive organizational initiatives that deliver performance and process improvements across a variety of sustaining engineering projects involving complex electro-mechanical, pneumatic, hardware and software systems
Fully participates in and successfully contributes to project teams typically including the following activities: product design and development, test of materials, establishment of specifications, report preparation, and test documentation.
Analyzes, synthesizes, and summarizes data communicating key product and business insights for leadership and stakeholders
Works independently to plan and schedule own activities necessary to meet timelines.
Designs and coordinates standard engineering tests and experiments.
Designs, procures, and fabricates tooling and fixtures.
Performs troubleshooting on new products/process problems as related to design, material, or process.
Leads product non-conformance and complaint investigations
Prepares standard reports/documentation to communicate results to technical community.
Responsible for engineering documentation including product specifications and design drawings .
Invents/creates concepts and designs for new products or product improvements , and submits idea disclosures.
May train and/or provide work direction to technicians.
Works cooperatively with operations, quality, regulatory, supplier engineering, marketing, and other functions to ensure project success.
Works effectively with team members across multiple sites and various regions of the world, as well as internal/external partners as necessary to achieve project objectives
In all actions, demonstrates a primary commitment to patient safety and product quality by maintaining compliance to all documented quality processes and procedures
Minimum Required Qualifications:
BS degree or more in Mechanical, Biomedical or a related Engineering field
5+ years of work experience in engineering (MS degree or higher may count as 2 years of work experience).
Highly self-motivated and able to manage schedule to meet critical deadlines
Independent thinker and skilled problem solver
Excellent organizational, communication, and collaboration skills
Willingness to work onsite at our Maple Grove, MN site
Preferred Qualifications
Medical device design experience
Experience with complex medical device systems
Experience with IEC 60601-1 Safety and EMC, RoHS/REACH, among other common electronic equipment and medical device compliance standards
Experience with sustaining engineering and commercial support
Base Salary Range:
Minimum Salary: $ 80100
Maximum Salary: $ 152200
Compensation for
exempt rolesmay also include variable compensation, i.e., annual bonus target and long-term incentives (subject to plan eligibility and other requirements).
Please be advised that certain US based positions, including without limitation field sales and service positions that call on hospitals and/or health care centers, require acceptable proof of COVID-19 vaccination status. Candidates will be notified during the interview and selection process if the role(s) for which they have applied require proof of vaccination as a condition of employment. Boston Scientific continues to evaluate its policies and protocols regarding the COVID-19 vaccine and will comply with all applicable state and federal law and healthcare credentialing requirements. As employees of the Company, you will be expected to meet the ongoing requirements for your roles, including any new requirements, should the Company’s policies or protocols change with regard to COVID-19 vaccination.
Among other requirements, Boston Scientific maintains specific prohibited substance test requirements for safety-sensitive positions. This role is deemed safety-sensitive and, as such, candidates will be subject to a prohibited substance test as a requirement. The goal of the prohibited substance testing is to increase workplace safety in compliance with the applicable law.
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