Boston Scientific
Process Development Engineer – Medical Devices
Location:
On-site (local travel only, no overnight)
Travel:
Up to 10% (local only)
Pay rate up to $56/hr
Position Overview We are seeking a motivated, collaborative, and creative individual to join a high-performing
Process Development team
focused on next‑generation technologies and products for advanced cardiac devices. This role offers strong opportunities for growth and will involve driving innovative technology solutions from concept to commercialization. You will partner cross‑functionally with a technically strong, experienced, and highly engaged team.
Key Responsibilities
Own equipment, processes, inspections, development builds, and drive improvements in associated technology and methodology.
Position future projects for success by reducing Human Visual Inspection (HVI) in manufacturing.
Manage processes and key deliverables through DV, PV, and commercial launch.
Collaborate with R&D, Equipment Engineering, Manufacturing Engineering, and Design Assurance to develop product concepts, equipment, inspections, and influence design specifications.
Provide Design for Manufacturability (DFM) input to engineering print packages.
Develop new assembly and inspection capabilities for complex equipment.
Train, mentor, and provide work direction to engineers and technicians; train manufacturing personnel as needed during validations.
Communicate technical data and recommendations clearly and concisely.
Solve complex technical problems in a hands‑on manner within a fast‑paced, dynamic environment.
Develop, write, and review process validation strategies and related deliverables (e.g., experiment reports, GR&R, TMV, IQ, FMEA).
Serve as a core team member, workstream lead, or extended team member on new product development projects.
Quality Systems Duties
Build quality into all aspects of work by maintaining compliance with applicable quality requirements.
Required Qualifications
Bachelor’s degree in engineering or relevant technical field.
Minimum of 4 years of professional experience in a related role.
Prior experience in medical device or other regulated industry.
Demonstrated cross‑functional collaboration and influence in technical environments.
Experience with automated inspection and/or assembly equipment.
Strong problem‑solving and root cause investigation skills.
Expertise in new product development and/or operations.
Experience with process verification and validation (TMVs, OQ/PQs).
Proficiency in statistical methods to drive improvements.
Strong written and verbal communication, decision‑making, and critical thinking skills.
Preferred Qualifications
Experience with Nitinol manufacturing.
Additional Notes
This position requires on‑site work.
Possible temp‑to‑hire opportunity for the right candidate, depending on budget.
Seniority level Mid‑Senior level
Employment type Contract
Job function Medical Equipment Manufacturing
Referrals increase your chances of interviewing at Boston Scientific by 2x
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On-site (local travel only, no overnight)
Travel:
Up to 10% (local only)
Pay rate up to $56/hr
Position Overview We are seeking a motivated, collaborative, and creative individual to join a high-performing
Process Development team
focused on next‑generation technologies and products for advanced cardiac devices. This role offers strong opportunities for growth and will involve driving innovative technology solutions from concept to commercialization. You will partner cross‑functionally with a technically strong, experienced, and highly engaged team.
Key Responsibilities
Own equipment, processes, inspections, development builds, and drive improvements in associated technology and methodology.
Position future projects for success by reducing Human Visual Inspection (HVI) in manufacturing.
Manage processes and key deliverables through DV, PV, and commercial launch.
Collaborate with R&D, Equipment Engineering, Manufacturing Engineering, and Design Assurance to develop product concepts, equipment, inspections, and influence design specifications.
Provide Design for Manufacturability (DFM) input to engineering print packages.
Develop new assembly and inspection capabilities for complex equipment.
Train, mentor, and provide work direction to engineers and technicians; train manufacturing personnel as needed during validations.
Communicate technical data and recommendations clearly and concisely.
Solve complex technical problems in a hands‑on manner within a fast‑paced, dynamic environment.
Develop, write, and review process validation strategies and related deliverables (e.g., experiment reports, GR&R, TMV, IQ, FMEA).
Serve as a core team member, workstream lead, or extended team member on new product development projects.
Quality Systems Duties
Build quality into all aspects of work by maintaining compliance with applicable quality requirements.
Required Qualifications
Bachelor’s degree in engineering or relevant technical field.
Minimum of 4 years of professional experience in a related role.
Prior experience in medical device or other regulated industry.
Demonstrated cross‑functional collaboration and influence in technical environments.
Experience with automated inspection and/or assembly equipment.
Strong problem‑solving and root cause investigation skills.
Expertise in new product development and/or operations.
Experience with process verification and validation (TMVs, OQ/PQs).
Proficiency in statistical methods to drive improvements.
Strong written and verbal communication, decision‑making, and critical thinking skills.
Preferred Qualifications
Experience with Nitinol manufacturing.
Additional Notes
This position requires on‑site work.
Possible temp‑to‑hire opportunity for the right candidate, depending on budget.
Seniority level Mid‑Senior level
Employment type Contract
Job function Medical Equipment Manufacturing
Referrals increase your chances of interviewing at Boston Scientific by 2x
#J-18808-Ljbffr