Sr Design Assurance Engineer
Veranex
Veranex's mission as an Innovation CRO is to improve patient outcomes by accelerating our clients' innovations to market. As the world's only end-to-end professional services firm focused on MedTech, we take clients' Vision to Velocity through our comprehensive service portfolio, with expertise in human centered design and product development, preclinical and clinical research, regulatory affairs, and market access and reimbursement consulting.
About This Role
- Lead risk management for novel and existing medical devices, including risk management plans and reports, hazard analyses and use, design, and process Failure Mode & Effects Analysis (FMEA).
- Plans, develops, and executes verification and validation testing for products under development.
- Provides input to development teams in the design of highly complex medical devices (including electrical, mechanical, software, drug, IVD). Provides quality insight and leadership on program teams and assists with establishing appropriate build quality controls appropriate with use.
- Develops, documents, and validates inspection and test methods to support development and manufacturing.
- Participate in the technical review of design input specifications and design documentation for new medical devices.
- Assists with implementing and maintaining a quality system that is compliant with relevant quality system regulation requirements. Participate in Quality System continuous improvement activities.
- Ensures the successful integration of quality assurance and regulatory compliance, working across multiple teams and medical device/equipment categories.
- Supports internal and external audit activities.
- Trains and mentors new and less experienced engineers. May provide performance feedback on performance of peers to functional management.
- Bachelor's degree in engineering or related field
- 3-6 years of relevant work experience in medical devices, or an equivalent combination of education, experience and training
- Working understanding of ISO 13483 and ISO 14971.
- Has experience in ISO10993, IEC60601, IEC62304, IEC62366, MDR and IVDR.
- Working understanding of Food & Drug Administration (FDA) Quality System regulations, European Active Implantable & Medical Device Regulations, and relevant medical device principles
- Excellent written and oral communication skills
- Excellent attention to detail
- Demonstrated experience with client management
- Experience with different quality management systems
- This is an onsite position with hybrid capabilities in Providence, RI or Minneapolis, MN
- Official communications will only come from company email addresses ending in @veranex.com.
- We will never ask you to send money or provide banking information at any stage of the recruitment process.
- Be cautious of unexpected emails and avoid opening suspicious links or attachments.
- When in doubt, contact us. If you have questions about the authenticity of a communication you've received, please contact our recruiting team at View email address on click.appcast.io before responding
$70.4k - $116.2k
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