Sr Test Engineer
Planet Pharma
Top 3 technical skills that are required for the role:
- Verification & Validation Strategy Leadership
- Test Method Development & Validation Expertise
- Execution Discipline & Regulatory Documentation
A DAY IN THE LIFE
Within our R&D Department in Neuromodulation, this employee will be part of a team that defines, develops and tests new products for the Neuromodulation business. The position responsibilities will primarily focus on system verification and validation (V&V) for Interventional products. This role is integral in the development cycle of any new product within this business. They will be responsible for partnering with Systems Development engineering lead and design teams, Quality engineers and Program managers to drive meaningful design inputs, robust designs and ultimately an efficient and effective V&V strategy. The position offers excellent opportunity for an engineer interested in defining and executing V&V strategies with robust test method validations to produce reliable and successful products. Candidates should have demonstrated ability to execute independently after receiving high level scope and constraints. Employee responsibilities may include the following: Develop comprehensive plans for verification testing, including test method validation Create verification protocols with sample size justifications and acceptance criteria definitions Drive design input verification for sterilized disposable instruments, including but not limited to system compatibility, reliability, mechanical and tissue performance, partnering with design quality, systems, mechanical and electrical engineering partners and laboratory technicians Develop test methods, test method validation plans, and test method validation reports Clearly document a verification body of evidence through regulatory submission ready engineering reporting Support design validation of user needs with real end-users in real or simulated use environments Support design reviews and risk management activities Partner with manufacturing, quality, marketing, human factors, and regulatory teams to ensure the design is verified in compliance with medical device standards Execute minimally invasive therapy procedures and products in soft tissue per medical device standards and internal procedures Effectively communicate and present test findings, analysis and conclusions cross-functionally Provide senior-level technical leadership to internal engineers and external development partnersQUALIFICATIONS SECTION
Must Have: Minimum Requirements To be considered for this role, please ensure the minimum requirements are evident on your resume. Bachelor’s degree in engineering or scientific discipline and 6+ years experience in technical testing or engineering experience OR Advanced Degree in engineering or scientific discipline and 4+ years experience in technical testing or engineering experience Experience leading system-level verification planning, execution, and documentation Experience supporting system-level validation planning, execution, and documentation Experience testing devices in ex-vivo tissue Basic knowledge of mechanical and electrical engineering fundamentals Basic knowledge of mechanical and electrical test equipment (ex. Instron, multimeter, etc.) Demonstrated ability to work both independently and in a cross-functional team environment Strong organization, prioritization, and communication skills Desired/Preferred qualifications History working in regulated industries such as medical, aerospace or defense Knowledge of IEC 60601 testing standards Knowledge of electrical safety testing and EMC testing Familiarity with Design for Reliability and Manufacturability (DRM) best practices (6 sigma) Experience performing system design input tracing to test results Experience working on systems that have mechanical, electrical and software elements Experience owning the systems engineering execution across the full V-model lifecycle #J-18808-Ljbffr Planet PharmaVacancy posted 1 day ago
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