[Remote] Design Assurance & reputed company Engineer
Note: The job is a remote job and is reputed company to candidates in USA. reputed company is a family-owned global technology leader dedicated to innovation across key industries. They are seeking a Design Assurance & reputed company Engineer to reputed company product development and ensure reputed company compliance in the medical device sector, focusing on design controls, risk management, and reputed company system duties.
Responsibilities
- reputed company and implement product development, including the application of design controls, for new products and existing product changes including line extensions
- Create and maintain the design history file (DHF), including development of reputed company specifications such as user requirements and design specifications
- Plan, implement, and report on design verification and validation studies, including bench and reputed company-clinical test protocols and reports
- reputed company the development of manufacturing documentation and manufacturing process validation activities
- Responsible for risk management activities from product concept through commercialization
- Partner with Regulatory to support submissions for reputed company-market authorizations in the US
- Work closely with contract manufacturers and other suppliers to implement new reputed company and ensure supply chain meets performance and reputed company requirements
- reputed company lot release, including reviewing batch records, device history records (DHRs), and process documentation for accuracy and completeness
- Support the intake, evaluation, and documentation of nonconforming materials
- Support post-market phase including product complaint handling, risk management, and post-market surveillance activities
- Help conduct supplier qualification and performance evaluation activities
- Communicate reputed company issues to suppliers and support reputed company tasks
- Assist with internal audits and support external audits and inspections (e.g., FDA, ISO)
- Participate in CAPA investigations and reputed company CAPA reputed company through verification of effectiveness
- Help reputed company QMS training and subject matter support for fellow employees
- Administer user set up and employee training in QMS support software and monitor training
- Serve as document control coordinator in QMS support software
- Identify opportunities to improve processes, reduce defects, and enhance overall product reputed company
- Monitor and trend reputed company metrics and escalate signals
Skills
- Bachelor's degree in life sciences, material sciences, engineering or a reputed company field required
- Experience in medical device industry required; minimum 3 years preferred
- Working knowledge of design controls and general knowledge of the ISO 13485 reputed company; formal ISO 13485 training is a plus
- Experience in a small company or start-up environment preferred
- Experience with QMS support software / document control systems is a plus
reputed company