Manager Systems Engineering

The Systems Engineering Manager facilitates the execution of strategic product development objectives by providing both technical leadership and direct systems engineering contributions across the product development lifecycle. This role leads a small team of Systems Engineers while actively participating in system architecture, requirements development, risk management, system integration, and verification activities. The Systems Engineering Manager partners closely with cross-functional teams to translate customer, clinical, business, and regulatory requirements into robust medical device solutions while continuously improving systems engineering processes, tools, and best practices.

ESSENTIAL DUTIES
• Leads and develops the Systems Engineering team.
• Generates and analyzes system architectures, requirements, and risk management artifacts.
• Communicates and coordinates with cross-functional teams.
• Provides technical leadership for system integration, verification, validation, and problem resolution.
• Advises teams on systems engineering tools, methods, and standards.
• Monitors work to ensure technical quality, effective execution, and schedule adherence.

COMPETENCIES
• Passion: Contagious excitement about the company – sense of urgency. Commitment to continuous improvement.
• Integrity: Commitment, accountability, and dedication to the highest ethical standards.
• Collaboration/Teamwork: Inclusion of Team Member regardless of geography, position, and product or service.
• Action/Results: High energy, decisive planning, timely execution.
• Innovation: Generation of new ideas from original thinking.
• Customer Focus: Exceed customer expectations, quality of products, services, and experience always present of mind.
• Emotional Intelligence: Recognizes, understands, manages one’s own emotions and is able to influence others. A critical skill for pressure situations.

QUALIFICATIONS
Education/Experience Required:
• Bachelor's degree in Systems Engineering, Biomedical Engineering, Electrical Engineering, Mechanical Engineering, Software Engineering, or a related discipline with a minimum of 10 years of relevant experience.
• Demonstrated experience leading cross-functional engineering teams.
• Direct experience with requirements development, traceability management, risk management, system architecture, and verification activities.
• Strong written and verbal communication skills.
Preferred:
• Previous people management experience.
• Direct experience developing regulated medical devices.
• Strong knowledge of ISO 14971, IEC 60601 series, IEC 62304, IEC 62366, and FDA design control requirements.
• Experience with requirements management and traceability tools such as IBM DOORS.
• Experience supporting FDA, EU MDR, and international regulatory submissions.

SUPERVISORY RESPONSIBILITIES:
• Directly supervise Systems Engineering team members including conducting performance reviews, providing performance feedback, establishing development goals, allocating resources, and supporting career growth.

WORK ENVIRONMENT
• Indoor open office environment
• Minimal noise volume typical to an office environment
• Extended hours when needed
• Kestra manufactures and provides life-saving products regulated by the Federal Food and Drug Administration and under contract with Medicare. Kestra maintains a drug free workplace and testing is a condition of employment post-offer.

PHYSICAL DEMANDS
• Frequent repetitive motions that may include wrists, hands and/or fingers, such as keyboard and mouse usage
• Frequent stationary position, often standing or sitting for prolonged periods of time
• Frequent computer use
• Frequent phone and other business machine use
• Occasional lifting required, typically between 2-15 pounds

TRAVEL
• Occasional travel may be required, 10%

OTHER DUTIES:
This job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the Team Member. Duties, responsibilities, and activities may change or new ones may be assigned at any time with or without notice.

BENEFITS:

Kestra offers a very competitive benefit package including Medical, Dental, 401K with Match, etc.

Pay equity is an important part of Kestra’s Culture. Our compensation ranges are guided by national and local salary surveys and take into consideration experience level and internal equity. Each role is benchmarked based on the job description provided If your qualifications and/or experience level are outside of the posted position, we encourage you to apply as we are growing fast and roles that are coming soon may not be posted.

Salary: Annualized at $170,000 - $196,000 plus bonus, depending on experience. Kestra Medical Technologies is an equal opportunity employer. Kestra Medical Technologies does not discriminate on the basis of race, color, religion, national origin, veteran status, age, sexual orientation, gender identity and/or expression, marital status, disability, physical or mental status or any other characteristic protected by law.

We are unable to sponsor or take over sponsorship of visas (any) at this time. Applicants must be eligible to work for any employer in the U.S.

Kestra manufactures and provides life-saving products regulated by the Federal Food and Drug Administration and under contract with Medicare.  Kestra maintains a drug free workplace and testing is a condition of employment.