Release Engineering Manager jobs in Sun Valley, NV

Company Description

ANEUVO is a Platform and Therapy Development company focused on treating chronic injuries and conditions that have not been curable through traditional pharmaceutical approaches. ANEUVO is developing breakthrough neuromodulation devices and bioelectronic medicine to treat diseases and injuries that are incurable with conventional therapies. We are building a cohesive team with complementary and multidisciplinary expertise to develop and bring our products to market.

Role Description: Engineering Manager with EE focus

This is a full-time on-site role for an Engineering Manager at ANEUVO in Westwood, CA. The Engineering Manager will be responsible for leading a team of engineers, overseeing software development projects, managing integration, and overseeing project management tasks. The Engineering Manager will be responsible for collaborating with multiple cross-functional teams to ensure successful product development and launch. This is a unique opportunity to work with products and technology that have a direct and immediate impact on improving human life. An ideal candidate has excellent social skills, demonstrates technical aptitude, and often exceeds expectations.

Key Responsibilities:

• Manages biomedical, electrical, firmware, or software engineers in the development of new products, features, and interfaces
• Coordinates the technical implementation of product changes, fixes, and improvements through task assignments, strategic timelines, and efficient processes
• Oversees and enforces thorough review and testing procedures
• Drafts and approves documentation for specifications, drawings, materials, architectures, test procedures, test reports, etc.
• Oversees project logistics and resource allocation
• Strives to improve efficiency and sustainability of processes and product designs, and to reduce waste
• Maintains high level expertise in the field of neuromodulation, neuroprostheses, and neuroengineering
• Helps to create and oversee project budgets and engages in cost management strategies
• Defines electrical specifications of the system
• System/circuit design and implementation
• Holds design reviews to show design meets target
• Defines, supports and/or executes bench top test plans
• Takes and support lab measurements to verify design and troubleshoot issues
• Develops engineering documentation and device/system verification
• Collaborates with quality, clinical and regulatory team members to ensure compliant processes
• Conducts responsibilities in a professional manner with the highest ethical and social conduct in all interactions
• Forges and maintains relationships with suppliers and customers
• Advocates on behalf of team members by securing adequate resources for success
• Values integrity and teamwork

Desired Skills:

• Excellent communication and interpersonal skills
• Personnel and project management skills
• Strategic thinking
• Critical thinking and problem-solving skills
• Adaptable to change and a fast-paced environment
• Organized and self-motivated to exceed expectations
• Agile project management experience
• Technical knowledge of medical electrical equipment
• Attention to detail and thorough documentation skills
• Strong public speaking and presentation skills
• Ability to work on multiple projects in various stages, simultaneously
• Flexible thinking, including the ability to pivot and try new approaches when faced with challenges
• Leadership, team-building, and mentoring skills

Qualifications:

• M.S or PhD degree in engineering
• Engineering Management and Team Leadership skills
• Minimum 7-10 years of professional experience in the field of electronics, electrical, software, or firmware, mechanical, neural engineering
• Minimum 3-5 years of management experience
• Experience in medical device, neurostimulation or neuromodulation field
• Master's degree in engineering or MBA is a plus
• Outcome-driven
• Experience with ISO 13485 and FDA regulation
• Knowledge in IEC 60601 Standard
• Knowledge in embedded system engineering
• Hands-on experience with Application Specific Integrated Circuit (ASIC) and PCB design, tapeout, verification and validation
• Hands-on experience with lab measurement and soldering
• Outstanding ability and knowledge in the field of EE
• Skilled in Altium, Cadence, Synopsis, Mentor Graphics,
• Resourceful and tenacious
• Preferred qualifications include experience in the medical device industry and familiarity with FDA and EU MDR regulations and guidelines.