VS
Research And Development Engineer
Accepting applicationsVeterans Sourcing Group, LLC · St Paul, MN
Contract Mid_senior
Posted
4 Sept
Category
Verification
Experience
Mid_senior
Country
United States
Engineer - R&D Engineer III
Location: Hybrid on-site in Weaver Lake, MN or Arden Hills, MN, 3 days onsite
Interview process: 2 rounds, 1st with HM and if called back panel.
Duration: 6 Months
Time: 08:00:AM - 04:30:PM
Job Description:
The Urology Research & Development (R&D) organization is seeking two highly skilled and motivated contract engineers to support the Valencia Technologies integration project through February 2027. In this role, you will support integration of the acquired company’s Design History File (DHF) to Boston Scientific compliance, with primary emphasis on design outputs, design verification prerequisite deliverables and execution, test method development and validation, technical problem-solving and issue resolution, and DHF documentation.
As a key team member, you will provide technical solutions and support under some guidance from our subject matter experts. You will utilize your background in mechanical and/or systems design, design verification, test method development and validation, verification testing, engineering documentation, and technical problem-solving.
Key Responsibilities:
Successfully completing engineering work in one or more of the following: design outputs; design verification prerequisite deliverables and execution; Design Verification test method development and validation; Essential Design Output identification; System/Subsystem/Component requirements tracing; and Design FMEA
Providing input to project goals and progress and recommending appropriate revisions.
Communicating progress, risks, and trade-offs of technical deliverables to R&D technical leadership and recommending revisions as needed.
Completing complex rationale on ability or inability to leverage acquired company documentation. Work is expected to result in efficient and effective integration of medical device technologies to the Boston Scientific portfolio.
Providing technical problem-solving and issue resolution, including assessing the feasibility and soundness of alternative engineering processes, products, equipment, or documentation approaches.
Completing clear and concise DHF and engineering documentation, including protocols, reports, rationales, design outputs, and verification-related deliverables.
Demonstrating Technology Development and Product Development system knowledge through delivery of high quality, high impact deliverables.
Qualifications:
BS or above in Mechanical Engineering, Biomedical Engineering, Electromechanical Engineering, or related field
4+ yrs of Medical Device engineering or related experience with bachelor’s degree, or 2+ yrs with Master’s
Strong mechanical and/or systems engineering and problem-solving skills and attention to detail
Ability to draw conclusions and make recommendations based on technical inputs from multiple and varied sources
Strong written and verbal communication, judgment, decision-making, collaboration, and critical thinking skills
Personal drive, individual accountability & a strong bias for action.
10% travel
Preferred Qualifications:
Previous experience at Boston Scientific
Familiarity with IEC 14708 and 45502 Active Implantable standards
Familiarity with IEC 60601 Medical Electrical Equipment standards
Experience with statistical techniques (Gauge R&R, Process Capabilities Studies) and Minitab
Experience in requirements tracing applications like Cognition Cockpit
Experience in single-use device or active implantable test methods and test method validation
Ability to build strong relationships across the organization and with external stakeholders
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Location: Hybrid on-site in Weaver Lake, MN or Arden Hills, MN, 3 days onsite
Interview process: 2 rounds, 1st with HM and if called back panel.
Duration: 6 Months
Time: 08:00:AM - 04:30:PM
Job Description:
The Urology Research & Development (R&D) organization is seeking two highly skilled and motivated contract engineers to support the Valencia Technologies integration project through February 2027. In this role, you will support integration of the acquired company’s Design History File (DHF) to Boston Scientific compliance, with primary emphasis on design outputs, design verification prerequisite deliverables and execution, test method development and validation, technical problem-solving and issue resolution, and DHF documentation.
As a key team member, you will provide technical solutions and support under some guidance from our subject matter experts. You will utilize your background in mechanical and/or systems design, design verification, test method development and validation, verification testing, engineering documentation, and technical problem-solving.
Key Responsibilities:
Successfully completing engineering work in one or more of the following: design outputs; design verification prerequisite deliverables and execution; Design Verification test method development and validation; Essential Design Output identification; System/Subsystem/Component requirements tracing; and Design FMEA
Providing input to project goals and progress and recommending appropriate revisions.
Communicating progress, risks, and trade-offs of technical deliverables to R&D technical leadership and recommending revisions as needed.
Completing complex rationale on ability or inability to leverage acquired company documentation. Work is expected to result in efficient and effective integration of medical device technologies to the Boston Scientific portfolio.
Providing technical problem-solving and issue resolution, including assessing the feasibility and soundness of alternative engineering processes, products, equipment, or documentation approaches.
Completing clear and concise DHF and engineering documentation, including protocols, reports, rationales, design outputs, and verification-related deliverables.
Demonstrating Technology Development and Product Development system knowledge through delivery of high quality, high impact deliverables.
Qualifications:
BS or above in Mechanical Engineering, Biomedical Engineering, Electromechanical Engineering, or related field
4+ yrs of Medical Device engineering or related experience with bachelor’s degree, or 2+ yrs with Master’s
Strong mechanical and/or systems engineering and problem-solving skills and attention to detail
Ability to draw conclusions and make recommendations based on technical inputs from multiple and varied sources
Strong written and verbal communication, judgment, decision-making, collaboration, and critical thinking skills
Personal drive, individual accountability & a strong bias for action.
10% travel
Preferred Qualifications:
Previous experience at Boston Scientific
Familiarity with IEC 14708 and 45502 Active Implantable standards
Familiarity with IEC 60601 Medical Electrical Equipment standards
Experience with statistical techniques (Gauge R&R, Process Capabilities Studies) and Minitab
Experience in requirements tracing applications like Cognition Cockpit
Experience in single-use device or active implantable test methods and test method validation
Ability to build strong relationships across the organization and with external stakeholders
Show more Show less