32 Boston Scientific jobs in Rogers

*** LOCAL CANDIDATES TO MINNETONKA, MN OR OPEN TO RELOCATE*** NO C2C***

Job Title:  Engineer, Research & Development

Location:  Minnetonka, MN (ON-SITE)

ID# SEDAA  42525

PAY RANGE:  50K - 64K/Annum

Description:

A qualified professional to lead and support medical device development projects through comprehensive project management and technical expertise. This role involves developing and maintaining detailed project plans, budgets, schedules, and risk registers to ensure successful execution and alignment with organizational goals.

• The candidate will contribute to the design and development of medical devices, ensuring that all products meet defined specifications and comply with applicable regulatory standards. Collaboration with engineering, quality, and regulatory teams will be essential to drive innovation and maintain compliance throughout the development process.
• Strong communication and collaboration skills are critical, as this role requires facilitating effective interactions among cross-functional teams and stakeholders. The ability to foster alignment and transparency across departments will be key to project success.
• In addition, the candidate will participate in and oversee product testing and validation activities to ensure that devices meet performance, safety, and quality requirements. Coordination with relevant teams will be necessary to support verification and validation efforts.
• Finally, the role includes preparing and maintaining documentation to support regulatory submissions and product lifecycle management. All documentation must be accurate, complete, and compliant with industry standards and internal policies.

*** LOCAL CANDIDATES TO ST. PAUL, MN OR OPEN TO RELOCATE*** NO C2C***

Job Title:  Test Technician

Location:   Irving, TX  (ON-SITE)

ID# SEDAA  42510

Training Days 8:45 to 3:30 Monday 7:00 to 3:30 Tuesday 6:00am to 2:30 next 8 days

PAY RANGE:  30K - 34K/Annum

Description:

Job Summary:

Working under general supervision, this position is responsible for the production of high-quality medical device instruments. This position includes detailed assembly and testing of various electronic components and finished devices in a controlled manufacturing environment.

Job Responsibilities:

• Performs testing of electronic components and assemblies using automated test equipment
• May perform mechanical assembly of electromechanical subassemblies and devices
• Ability to read, comprehend and follow written procedures; understand and follow verbal instructions. May instruct others in the use of all manuals, test procedures and documentation associated with specialized equipment.
• Reads and interprets engineering drawings, schematics and complex test procedures.
• Participates in continuous improvement/quality initiatives in order to enhance production processes to achieve quality and profitability metrics.
• Maintains accurate records to ensure Device History Records and quality documents are accurate, all parts are traceable and quality issues can be addressed to assure the quality of all products.
• Prioritizes work by determining the sequencing and timing of different jobs based on precedence and importance.
• Positively represents the company during tours by demonstrating techniques and sharing appropriate information.
• Supports all Company initiatives as identified by management and in support of Quality Management Systems (QMS), Environmental Management Systems (EMS), and other regulatory requirements.
• Complies with U.S. Food and Drug Administration (FDA) regulations, ISO or other regulatory requirements, Company policies, operating procedures, processes, and task assignments.
• Adheres to all environmental, health and safety SOP’s, equipment, policies and procedures, including any department specific requirements.
•  Maintains positive and cooperative communications and collaboration with all levels of employees, customers, contractors, and vendors.

Minimum Qualifications:

• Experience with electronic assembly and test in a medical device industry preferred.
• High School Diploma or equivalency is required, preferred AAS
• 2 or more years experience with electromechanical assemblies/electronic manufacturing, technical certifications, etc. preferred

Preferred Qualifications:

• Experience in troubleshooting equipment, building and or testing of electronic assemblies
• Working knowledge of IPC standards and use of complex tools and equipment specific to functional areas
• Experience in GMP, ISO, and FDA controlled environments preferred
• Ability to work within a team and as an individual contributor in a fast-paced, changing environment.
• Strong verbal and written communications with ability to effectively communicate at multiple levels in the organization.
• Multitasks, prioritizes and meets deadlines in timely manner.
• Strong organizational and follow-up skills, as well as attention to detail.
• Ability to maintain regular and predictable attendance.
• Ability to work scheduled overtime as required is preferred.
• Ability to hand and lift up to 25 lbs. as needed for specific job functions
• Must be able to sit and/or stand for long periods of time.
• Ability to frequently sit, stand, walk, reach within hands and arm’s length, stoop, kneel and crouch.

*** LOCAL CANDIDATES TO ST. PAUL, MN OR OPEN TO RELOCATE*** NO C2C***

Job Title:   Sr Electrical EngineerLocation:   St Paul,  MN (ON-SITE)ID# SEDAA  42306 Days/Hours: Mon – Friday 8:00am to 5:00pm

PAY RANGE : 35/hr - 47/hr 

Description:

• Selected Candidate will start ASAP after screenings have cleared.
• Ability to travel approximately 10%, including internationally.

Skills: 

• Relevant work experience in performing the layout, construction, and evaluation of a variety of prototype Printed Circuit Boards, fixtures and tools.
• Demonstrated ability to develop new design features as part of existing systems.
• Documented record of delivering tool engineering information which adds value to management’s decision-making process.
• Demonstrated ability to understand and comply with applicable FDA regulations and Company operating procedures, processes, policies and tasks. Advanced personal computer skills, including spreadsheet, word processing, database management, and specialized applications.
• Advanced credential or professional certification in a relevant discipline/concentration desired. Six-Sigma knowledge and experience desired.
• Training and experience in manufacturing processes and methods desired, especially in the manufacturing of medical devices.
• Experience working in a broader enterprise/cross-division business unit model preferred.
• Ability to work in a highly matrixed and geographically diverse business environment. Ability to work within a team and as an individual contributor in a fast-paced, changing environment.
• Ability to leverage and/or engage others to accomplish projects.
• Strong verbal and written communications with ability to effectively communicate at multiple levels in the organization.
• Multitasks, prioritizes and meets deadlines in timely manner.
• Strong organizational and follow-up skills, as well as attention to detail.
• Ability to travel approximately 10%, including internationally.

Education: 

• Bachelor's Degree In Electrical Engineering or related engineering field.

Duties:

• Lays out and constructs a variety of prototype tools and fixtures required for development purposes.
• Conducts evaluations, tests and analyses related to feasibility and function.
• Performs troubleshooting and fault isolation activities on a variety of breadboards and hybrids.
• Conducts measurements specified in design verification plans, documents and tabulates results, and provides engineering test reports.
• Documents custom tools with specifications, schematics and mechanical layouts to support document control and tool release.
• Complies with U.S. Food and Drug Administration (FDA) regulations, other regulatory requirements, Company policies, operating procedures, processes, and task assignments. Maintains positive and cooperative communications and collaboration with all levels of employees, customers, contractors, and vendors.

Job Title: R&D Engineer II

Duration: 12+ Months (Possible temp to hire)

Location: Maple Grove, MN 55311

Onsite Role

Responsibilities:

• MUST have CAD/SolidWorks experience
• Develops products, materials, processes, or equipment for projects of moderate complexity.
• Compiles, analyzes, and reports operational, test, and research data to establish performance standards for newly designed or modified products, processes, and materials.
• Fully participates in and successfully contributes to project teams typically including the following activities: product design and development, test of materials, preparation of specifications, process capability studies, research investigations (animal and clinical studies), report preparation, and process/test documentation.
• 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.
• Summarizes, analyzes, and draws conclusions from test results.
• Prepares standard reports/documentation to communicate results to technical community.
• Responsible for engineering documentation.
• Invents/ creates concepts and designs for new products/processes, and submits idea disclosures.
• May train and/or provide work direction to technicians.
• Works cooperatively with process development, quality, manufacturing, regulatory, clinical, and marketing to ensure project success.

Education/Experience:

• 2 - 4 Years with BS degree in ME or Bioengineering
• Molded component development preferred.
• Medical Device experience highly preferred
• MUST have CAD/SolidWorks experience
• MS Office
• PDP (Product development process)/TPD system knowledge

Work Hours: Flexible schedule with core hours from 9 AM to 3 PM. Occasional early or late meetings may be required. Onsite days may vary weekly based on testing needs.

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Position Overview:

We are seeking a Sustaining and R&D Engineer (Engineer III) with approximately 8 years of experience to support both sustaining engineering and new product development (NPD) initiatives. This role is ideal for a detail-oriented, hands-on mechanical engineer with strong communication skills and a background in SolidWorks modeling and test fixture development. This engineer will be part of a high-energy, fast-paced culture.

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Key Responsibilities:

Sustaining Engineering:

· Provide mechanical expertise to support CAPA and design change activities

· Create solutions for design changes to address performance and end-of-life activities

· Design and assemble test fixtures (simple to mid-level complexity).

· Perform design verification testing and complete documentation for CAPAs and design changes.

· Author Design Verification protocols and reports related to design changes.

New Product Development (NPD):

· Contribute to housing and closure design for capital equipment.

· Support compliance testing processes.

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Required Skills & Experience:

· SolidWorks proficiency – essential for modeling and fixture design.

· Experience with test fixture development and testing.

· Exposure to electrical systems is a plus.

· Strong documentation and protocol ownership experience.

· Excellent attention to detail and communication skills.

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Preferred Qualifications:

· Background in mechanical engineering with exposure to electrical components.

· Experience in regulated environments (medical device or similar industries).

· Ability to adapt to changing onsite schedules and collaborate across teams.

· Familiarity with injection molding and thermoplastics.

Responsibilities:

• Lead hands-on development and prototyping of novel cardiac devices.
• Contribute to device design, development, and iteration under tight resource constraints.
• Support and/or lead preclinical animal studies – design, execution, and evaluation.
• Collaborate with cross-functional teams to advance concepts from R&D through clinical testing.
• Think creatively to solve technical challenges and innovate within limited budgets and timelines.
• Provide leadership potential for the growing R&D team as the company expands.

Experience Required:

• 2+ years’ experience in medical device R&D (structural heart, cardiovascular, or catheter development)
• Hands-on builder and problem-solver – enjoys prototyping, testing, and iterating in the lab.
• Experience with implants, delivery systems, and structural heart/tissue dynamics.
• Animal study experience – design, leadership, and/or execution.
• Bonus: Clinical exposure (training physicians, case support, imaging analysis).
• Startup mindset – resourceful, adaptable, comfortable working in a fast-paced, lean environment.
• Strong communication skills, with ability to collaborate across teams and with physicians.
• Creative thinker who contributes ideas, not just execution.

JCW is working on an exciting search for a 6 month temp to perm contract with a growing medical device company seeking a skilled Senior R&D Engineer to support the design, integration, and optimization of medical devices.

This role is onsite role out of Maple Grove, MN.

Key Responsibilities:

• Serve as the R&D point of contact for sustaining efforts and contract manufacturer interactions.
• Evaluate and implement continuous improvement changes to enhance user experience.
• Collaborate with cross-functional teams to assess technical impacts of design adjustments.

Qualifications:

• Bachelor’s or Master’s degree in Mechanical or Biomedical Engineering.
• 4+ years of experience in medical device R&D, with emphasis on sustaining engineering or design iteration.
• Solid understanding of mechanical systems and design validation.
• Familiarity with regulated development environments and working with CMOs (Contract Manufacturing Organizations).
• Strong communication and problem-solving skills.

For more information on this role please apply or email Megan at

JCW is working on an exciting search for a Principal R&D Engineer with a growing medical device company seeking a skilled Principal R&D Engineer to support the design, integration, and optimization of medical devices.

This role is onsite role out of Maple Grove, MN.

Key Responsibilities:

• Serve as the R&D point of contact for sustaining efforts and contract manufacturer interactions.
• Evaluate and implement continuous improvement changes to enhance user experience.
• Collaborate with cross-functional teams to assess technical impacts of design adjustments.

Qualifications:

• Bachelor’s or Master’s degree in Mechanical or Biomedical Engineering.
• 8+ years of experience in medical device R&D, with emphasis on sustaining engineering or design iteration.
• Solid understanding of mechanical systems and design validation.
• Familiarity with regulated development environments and working with CMOs (Contract Manufacturing Organizations).
• Strong communication and problem-solving skills.

For more information on this role please apply or email Megan at

Job Title: Sr. R&D Engineer - Medical Device

Duration: 12+ Months (Possible extension)

Location: Maple Grove, MN 55311

Onsite Role

Responsibilities:

• Seeking a Test Method Development Engineer to support the creation, validation, and continuous improvement of test methods within our product development process.
• This role requires strong technical expertise in experimental design, risk control, and regulatory compliance.
• Will ensure that test methods are scientifically sound, accurately measure product performance, and meet all applicable standards

Test Method Development:

• Design, develop, and document new test methods to support product verification.
• Evaluates the appropriateness and applicability of the test method to measure the specification.
• Create test instructions following company work instructions and applicable standards (ISO 10555, 21 CFR 820.30, ISO 13485, etc.).
• Evaluates the measurement accuracy and precision against the tolerance requirements.

Risk Management & Controls:

• Apply risk-based thinking to identify potential sources of variability or error in test methods.
• Incorporate controls that ensure measurement accuracy, repeatability, and reproducibility.
• Evaluate and mitigate risks related to equipment, operator execution, and environmental factors.

Design & Technical Integration:

• Collaborate with R&D, Design Engineering, Packaging Engineering and Quality teams to align test methods with product design inputs and requirements.
• Interpret product design intent to establish relevant test criteria and tolerances.
• Assess the impact of design or process changes on existing test methods and update documentation accordingly.

Validation & Compliance:

• Support test method validation activities via Design Quality.
• Ensure compliance with internal SOPs, regulatory requirements, and Good Documentation Practices (GDP).
• Maintain test method traceability to design specifications, risk analyses, and verification plans.
• Ensures test equipment and instruments are calibrated and qualified, if applicable.

Education/Experience:

• Bachelor’s degree in engineering, physics, math, or other science discipline, or equivalent.
• Min of 4 years experience in design quality, R&D, or product development engineering in Medtech /regulated industry experience; or equivalent combination of education and experience
• Understanding and demonstrated use of industry standards (e.g. IEC 60601, IEC 62304). within product design and development process
• Strong ability to navigate ambiguous situations in a collaborative, innovative, and people-centric team environment.
• Knowledge of key regulatory requirements including ISO 13485 Quality Management Systems, ISO 14971 Risk Management, 21 CFR 820, and EU MDR.

Responsibilities:

• Lead hands-on development and prototyping of novel cardiac devices.
• Contribute to device design, development, and iteration under tight resource constraints.
• Support and/or lead preclinical animal studies design, execution, and evaluation.
• Collaborate with cross-functional teams to advance concepts from R&D through clinical testing.
• Think creatively to solve technical challenges and innovate within limited budgets and timelines.
• Provide leadership potential for the growing R&D team as the company expands.

Experience Required:

• 2+ years experience in medical device R&D (structural heart, cardiovascular, or catheter development)
• Hands-on builder and problem-solver enjoys prototyping, testing, and iterating in the lab.
• Experience with implants, delivery systems, and structural heart/tissue dynamics.
• Animal study experience design, leadership, and/or execution.
• Bonus: Clinical exposure (training physicians, case support, imaging analysis).
• Startup mindset resourceful, adaptable, comfortable working in a fast-paced, lean environment.
• Strong communication skills, with ability to collaborate across teams and with physicians.
• Creative thinker who contributes ideas, not just execution.

Job Title: Sr. R&D Engineer - Medical Device

Duration: 12+ Months (Possible extension)

Location: Maple Grove, MN 55311

Onsite Role

Responsibilities:

• Seeking a Test Method Development Engineer to support the creation, validation, and continuous improvement of test methods within our product development process.
• This role requires strong technical expertise in experimental design, risk control, and regulatory compliance.
• Will ensure that test methods are scientifically sound, accurately measure product performance, and meet all applicable standards

Test Method Development:

• Design, develop, and document new test methods to support product verification.
• Evaluates the appropriateness and applicability of the test method to measure the specification.
• Create test instructions following company work instructions and applicable standards (ISO 10555, 21 CFR 820.30, ISO 13485, etc.).
• Evaluates the measurement accuracy and precision against the tolerance requirements.

Risk Management & Controls:

• Apply risk-based thinking to identify potential sources of variability or error in test methods.
• Incorporate controls that ensure measurement accuracy, repeatability, and reproducibility.
• Evaluate and mitigate risks related to equipment, operator execution, and environmental factors.

Design & Technical Integration:

• Collaborate with R&D, Design Engineering, Packaging Engineering and Quality teams to align test methods with product design inputs and requirements.
• Interpret product design intent to establish relevant test criteria and tolerances.
• Assess the impact of design or process changes on existing test methods and update documentation accordingly.

Validation & Compliance:

• Support test method validation activities via Design Quality.
• Ensure compliance with internal SOPs, regulatory requirements, and Good Documentation Practices (GDP).
• Maintain test method traceability to design specifications, risk analyses, and verification plans.
• Ensures test equipment and instruments are calibrated and qualified, if applicable.

Education/Experience:

• Bachelor’s degree in engineering, physics, math, or other science discipline, or equivalent.
• Min of 4 years experience in design quality, R&D, or product development engineering in Medtech /regulated industry experience; or equivalent combination of education and experience
• Understanding and demonstrated use of industry standards (e.g. IEC 60601, IEC 62304). within product design and development process
• Strong ability to navigate ambiguous situations in a collaborative, innovative, and people-centric team environment.
• Knowledge of key regulatory requirements including ISO 13485 Quality Management Systems, ISO 14971 Risk Management, 21 CFR 820, and EU MDR.