The Role
At QuidelOrtho, we’re advancing the power of diagnostics for a healthier future for all. Join our mission as our next Senior Manager, Systems Engineering, supporting our Point-of-Care instruments.
This Senior Manager of Systems Engineer provides technical leadership and accountability for the development of complex, multi-disciplinary systems—spanning hardware, software, consumable and assay integration in complex diagnostic systems. The role will lead system design efforts to collaborate with engineers, scientists, and cross-functional partners to investigate, design, and resolve system- level technical challenges.
This position will be onsite full-time in San Diego, CA (Summers Ridge – Sorrento Valley).
The Responsibilities
Systems Engineering & Integration
- Systems lead in new product development programs
- Systems Engineering subject matter expert within systems team
- Oversee the architecture, integration, and verification of complex diagnostic systems, ensuring alignment with product requirements and regulatory standards.
- Manage integration activities between external hardware/firmware development partners and internal software engineering teams
- Ensures accurate documentation of system requirements, interface specifications, and integration test plans data, and decisions
- Provides solutions to complex system-level technical problems
- Collaborates cross-functionally to define, decompose, verify, and validate system requirements
- Conduct system level risk analysis and ensure mitigation strategies are implemented
- Ensure compliance with relevant ISO standards (ISO 14971, IEC 62366, IEC 60601, etc.)
- Interfaces with manufacturing partners for effective system design transfer
Cross-Functional Leadership
- Serve as the technical liaison between partners and internal teams
- Technical Lead for cross-functional project teams including but not limited to R&D, Quality, Manufacturing, Regulatory, Clinical Affairs.
- Facilitate effective communication and problem-solving across distributed teams
- Drive technical decision-making and resolve integration challenges
- Present technical updates to senior leadership and stakeholders
Mentorship and Technical Guidance
- Mentor and provide technical guidance to junior engineers on system engineering principles and best practices
- Foster a culture of continuous improvement and technical excellence
- Keep abreast and share knowledge of updates to technical standards
- Perform other work-related duties as assigned.
The Individual
Required:
- Minimum of 10+ years’ experience with bachelor’s degree in engineering or related field, master’s degree preferred; and/or equivalent combination of education and experience.
- Proven track record of successfully bringing medical devices or Point of Care IVD instruments Demonstrated experience leading a systems design effort from concept to commercial launch in a regulated environment.
- Experience in medical devices/diagnostics and regulated environments
- Experience managing external development partners and/or working with contract manufacturing partners
- Experience and training in a specific discipline such as Mechanical,
- Electrical, Fluidics or SW engineering working knowledge in both hardware and software systems
- Strong Familiarity with ISO 13485, IEC 62366, IEC 60601, ISO 14971 standards
- Understanding of verification and validation strategies for complex systems
- Proven ability to lead without direct authority and influence cross-functional teams
- Strong communication, analytical, and teamwork skills
- Ability to travel up to 10%
- This position is not currently eligible for visa sponsorship.
The Key Working Relationships
Internal Partners:
- Engineering Team
- Program Managers
- Assay Development Scientists
- Manufacturing Team
- Design Quality
- Regulatory Affairs
External Partners:
- Contract design and manufacturers
- Electrical Safety Test Contacts
- Vendors
How We Work
At QuidelOrtho, our culture is shaped by four core behaviors that guide how we collaborate, make decisions, and support each other and those we serve. The ideal candidate will exhibit these behaviors, as we believe they9re essential to how we thrive as a team and achieve meaningful impact:
- Thrive Together 6 Collaborate intentionally, grow as a team
- Make It Happen 6 Focus on priorities, embrace continuous improvement
- Commit to Service 6 Cultivate a service mindset
- Embrace Inclusion 6 Be open and authentic, welcome diverse perspectives
The Work Environment
The work environment characteristics are representative of a manufacturing, laboratory, or warehouse environment and include handling of viral and bacterial hazards, potentially hazardous chemicals, as well as infectious or potentially infectious bodily fluids, tissues, and samples. Up to 75% of the time at desk, standing or sitting extended periods of time. Flexible work hours to meet project deadlines
Physical Demands
No strenuous physical activity required. Occasional light lifting of materials may be needed. Substantial time will be spent in virtual or in-person meetings, engaging with customers, and working on scientific content and documentation.
Salary Transparency
The salary range for this position takes into account a wide range of factors including education, experience, knowledge, skills, geography, and abilities of the candidate, in addition to internal equity and alignment with market data. At QuidelOrtho, it is not typical for an individual to be hired at or near the top range for their role and compensation decisions are dependent on the facts and circumstances of each case. The salary range for this position is $165,000 to $180,000 and is bonus eligible. QuidelOrtho offers a comprehensive benefits package including medical, dental, vision, life, and disability insurance, along with a 401(k) plan, employee assistance program, Employee Stock Purchase Plan, paid time off (including sick time), and paid Holidays. All benefits are non-contractual, and QuidelOrtho may amend, terminate, or enhance the benefits provided, as it deems appropriate.
