Bayside Solutions
Verification and Validation Engineer/Senior V&V Engineer
Bayside Solutions, Fremont, California, us, 94537
Overview
Verification and Validation Engineer/Senior V&V Engineer This range is provided by Bayside Solutions. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more. Base pay range $120,000.00/yr - $150,000.00/yr This is for mechanical engineering (physical testing). If you're system/software base, please do not apply Duties and Responsibilities
Conduct design verification and validation testing for product development activities Support all technical aspects of the product and instruments. Support regulatory requirements. Support the design control process. Support sustaining engineering activities with root cause and engineering analysis. Lead the engineering change process. In the event of potential non-compliance with applicable standards or regulations (e.g. FDA QSRs, ISO 13485, or ISO14971), the employee has the authority to hold any product or QA/RA documentation from shipment or further processing. The employee has the responsibility to report any instances to their direct supervisor or above. The V&V Engineer must at all times act and conduct company business in an honest, ethical, and strictly legal manner, complying with the Code of Conduct, other company policies, the AdvaMed Code, and all applicable laws and regulations, whether national, regional, state, or local. This individual is encouraged, expected, and required to report any suspected violations of laws, regulations, the Code, or any other Company policy, and all other suspected unethical behavior. The company does not tolerate retaliation in connection with making good faith reports of suspected violations. Be the verification and validation lead assisting the product development group in developing products to ensure constantly improved instrumentation and cutting-edge technology. Write protocols, assessments, conduct testing, and write test reports (e.g., performance, simulated use). As needed, source appropriate vendors to conduct testing and oversee their testing Requirements and Qualifications
Currently or recently served as V&V engineer for a high-growth, medical device organization whose products are marketed to a medical specialty practice and worked in that capacity for a minimum of 3 years. Experience in orthopedics is highly desired; spine experience is also a plus. Exceptional organization/planning skills (e.g., scheduling) and display initiative and perseverance in meeting deadlines. Good technical writing skills with attention to detail. Currently or recently performed testing to established standards (i.e., ISO, ASTM). Have a demonstrated ability to communicate effectively and work well with co-workers, surgeons, clinicians, and distributor reps. Have a working cross-disciplinary understanding of a medical device business, emphasizing engineering, manufacturing, operations, R&D, product marketing, clinical and regulatory, and quality assurance. Be known as a person who has high integrity, sound character, a tremendous work ethic, and the passion to succeed. Currently or recently designed and fabricated mechanical test fixtures to perform mechanical testing using machining (e.g., mill, lathe) or 3D printing. A passion for supporting an emerging company and sustaining high growth through engineering support. Desired Skills and Experience
design verification, validation testing, product development, technical support, regulatory requirements, design control process, sustaining engineering, root cause analysis, engineering analysis, engineering change process, FDA QSRs, ISO 13485, ISO14971, protocol writing, performance testing, simulated use testing, test reports, vendor sourcing, vendor management, medical device, orthopedics, spine, organization skills, planning, scheduling, technical writing, ISO standards, ASTM standards, cross-disciplinary collaboration, engineering, manufacturing, operations, R&D, product marketing, clinical, regulatory, quality assurance, mechanical test fixtures, fixture design, fabrication, machining, mill, lathe, 3D printing, mechanical testing Bayside Solutions, Inc. may collect your personal information during the position application process. Please reference Bayside Solutions, Inc.'s CCPA Privacy Policy at www.baysidesolutions.com. Seniority level
Mid-Senior level Employment type
Full-time Job function
Engineering, Quality Assurance, and Research Note: This refinement removes boilerplate job board content and keeps the core responsibilities, qualifications, and legal disclosures relevant to the role.
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Verification and Validation Engineer/Senior V&V Engineer This range is provided by Bayside Solutions. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more. Base pay range $120,000.00/yr - $150,000.00/yr This is for mechanical engineering (physical testing). If you're system/software base, please do not apply Duties and Responsibilities
Conduct design verification and validation testing for product development activities Support all technical aspects of the product and instruments. Support regulatory requirements. Support the design control process. Support sustaining engineering activities with root cause and engineering analysis. Lead the engineering change process. In the event of potential non-compliance with applicable standards or regulations (e.g. FDA QSRs, ISO 13485, or ISO14971), the employee has the authority to hold any product or QA/RA documentation from shipment or further processing. The employee has the responsibility to report any instances to their direct supervisor or above. The V&V Engineer must at all times act and conduct company business in an honest, ethical, and strictly legal manner, complying with the Code of Conduct, other company policies, the AdvaMed Code, and all applicable laws and regulations, whether national, regional, state, or local. This individual is encouraged, expected, and required to report any suspected violations of laws, regulations, the Code, or any other Company policy, and all other suspected unethical behavior. The company does not tolerate retaliation in connection with making good faith reports of suspected violations. Be the verification and validation lead assisting the product development group in developing products to ensure constantly improved instrumentation and cutting-edge technology. Write protocols, assessments, conduct testing, and write test reports (e.g., performance, simulated use). As needed, source appropriate vendors to conduct testing and oversee their testing Requirements and Qualifications
Currently or recently served as V&V engineer for a high-growth, medical device organization whose products are marketed to a medical specialty practice and worked in that capacity for a minimum of 3 years. Experience in orthopedics is highly desired; spine experience is also a plus. Exceptional organization/planning skills (e.g., scheduling) and display initiative and perseverance in meeting deadlines. Good technical writing skills with attention to detail. Currently or recently performed testing to established standards (i.e., ISO, ASTM). Have a demonstrated ability to communicate effectively and work well with co-workers, surgeons, clinicians, and distributor reps. Have a working cross-disciplinary understanding of a medical device business, emphasizing engineering, manufacturing, operations, R&D, product marketing, clinical and regulatory, and quality assurance. Be known as a person who has high integrity, sound character, a tremendous work ethic, and the passion to succeed. Currently or recently designed and fabricated mechanical test fixtures to perform mechanical testing using machining (e.g., mill, lathe) or 3D printing. A passion for supporting an emerging company and sustaining high growth through engineering support. Desired Skills and Experience
design verification, validation testing, product development, technical support, regulatory requirements, design control process, sustaining engineering, root cause analysis, engineering analysis, engineering change process, FDA QSRs, ISO 13485, ISO14971, protocol writing, performance testing, simulated use testing, test reports, vendor sourcing, vendor management, medical device, orthopedics, spine, organization skills, planning, scheduling, technical writing, ISO standards, ASTM standards, cross-disciplinary collaboration, engineering, manufacturing, operations, R&D, product marketing, clinical, regulatory, quality assurance, mechanical test fixtures, fixture design, fabrication, machining, mill, lathe, 3D printing, mechanical testing Bayside Solutions, Inc. may collect your personal information during the position application process. Please reference Bayside Solutions, Inc.'s CCPA Privacy Policy at www.baysidesolutions.com. Seniority level
Mid-Senior level Employment type
Full-time Job function
Engineering, Quality Assurance, and Research Note: This refinement removes boilerplate job board content and keeps the core responsibilities, qualifications, and legal disclosures relevant to the role.
#J-18808-Ljbffr