Junior Product Manager
ChromoLogic LLC, Monrovia, CA, United States
Join a Breakthrough Scientific Research Team Driving Innovation
Are you excited by the intersection of biology, engineering, and cutting‑edge medical technology? Do you love turning complex technical ideas into real‑world products that improve patient outcomes? If so, this is your chance to step into a high‑impact role at a fast‑moving medical device startup with big ambitions.
We’re looking for a
curious, proactive, detail‑driven Junior Product Manager
to help bring innovative, software‑enabled medical technologies from concept to market. You’ll collaborate daily with engineers, scientists, and regulatory experts—not from the sidelines, but hands‑on, influencing decisions that shape the future of patient care.
If you thrive in fast‑paced environments, love solving interdisciplinary problems, and want to grow quickly as a product leader, we’d love to meet you.
ChromoLogic LLC (www.chromologic.com) is a world‑class innovation center with advanced scientific research and development in the medical, aerospace and security markets.
What You’ll Do
Partner closely with R&D, regulatory, and quality teams to support product development and design control activities under
FDA 21 CFR Part 820
and
IEC 62304
for medical device software
Translate user needs into clear product requirements
and success metrics for emerging hardware–software systems
Coordinate verification, validation, and usability testing—ensuring every requirement has proper traceability
Maintain and organize
DHFs , risk analyses, and other quality system documentation with precision
Contribute to
regulatory submissions
(e.g., 510(k), De Novo) and participate in FDA pre‑submission discussions
Collaborate with software teams to prioritize bugs, features, and updates that align with clinical workflows and user insights
Support agile processes—sprint planning, backlog management, and documentation—using tools like
Jira
&
Confluence
Assist in post‑market monitoring, performance tracking, data analysis, and CAPA activities
Analyze competitive products, market trends, and unmet needs to guide product strategy and differentiation opportunities
What You Bring
Bachelor’s degree in
Biology, Bioengineering, Biomedical Engineering , or related technical field
1–3 years
of experience in
medical device product management, regulatory support, or R&D coordination
(internships count)
Working knowledge of
FDA design controls, software validation, and risk management principles
Ability to excel in a dynamic, cross‑functional, startup environment where iteration is fast and teamwork is essential
Strong communication and documentation skills—comfortable shifting between technical deep dives and high‑level stakeholder discussions
Nice‑to-Haves
Exposure to
SaMD (Software as a Medical Device)
or connected health platforms
Experience with early-phase product testing, clinical collaboration, or pilot deployments
Passion for scaling medical innovations that merge biology, engineering, and digital technology
What We Offer
Competitive salary and benefits package
A mission‑driven culture where
discovery and innovation
are at the heart of everything
Close collaboration with scientists and leaders shaping breakthrough research
A chance to build something meaningful—your systems, your ideas, your leadership
Flexible environment, high ownership, and the ability to make an immediate impact
#J-18808-Ljbffr
We’re looking for a
curious, proactive, detail‑driven Junior Product Manager
to help bring innovative, software‑enabled medical technologies from concept to market. You’ll collaborate daily with engineers, scientists, and regulatory experts—not from the sidelines, but hands‑on, influencing decisions that shape the future of patient care.
If you thrive in fast‑paced environments, love solving interdisciplinary problems, and want to grow quickly as a product leader, we’d love to meet you.
ChromoLogic LLC (www.chromologic.com) is a world‑class innovation center with advanced scientific research and development in the medical, aerospace and security markets.
What You’ll Do
Partner closely with R&D, regulatory, and quality teams to support product development and design control activities under
FDA 21 CFR Part 820
and
IEC 62304
for medical device software
Translate user needs into clear product requirements
and success metrics for emerging hardware–software systems
Coordinate verification, validation, and usability testing—ensuring every requirement has proper traceability
Maintain and organize
DHFs , risk analyses, and other quality system documentation with precision
Contribute to
regulatory submissions
(e.g., 510(k), De Novo) and participate in FDA pre‑submission discussions
Collaborate with software teams to prioritize bugs, features, and updates that align with clinical workflows and user insights
Support agile processes—sprint planning, backlog management, and documentation—using tools like
Jira
&
Confluence
Assist in post‑market monitoring, performance tracking, data analysis, and CAPA activities
Analyze competitive products, market trends, and unmet needs to guide product strategy and differentiation opportunities
What You Bring
Bachelor’s degree in
Biology, Bioengineering, Biomedical Engineering , or related technical field
1–3 years
of experience in
medical device product management, regulatory support, or R&D coordination
(internships count)
Working knowledge of
FDA design controls, software validation, and risk management principles
Ability to excel in a dynamic, cross‑functional, startup environment where iteration is fast and teamwork is essential
Strong communication and documentation skills—comfortable shifting between technical deep dives and high‑level stakeholder discussions
Nice‑to-Haves
Exposure to
SaMD (Software as a Medical Device)
or connected health platforms
Experience with early-phase product testing, clinical collaboration, or pilot deployments
Passion for scaling medical innovations that merge biology, engineering, and digital technology
What We Offer
Competitive salary and benefits package
A mission‑driven culture where
discovery and innovation
are at the heart of everything
Close collaboration with scientists and leaders shaping breakthrough research
A chance to build something meaningful—your systems, your ideas, your leadership
Flexible environment, high ownership, and the ability to make an immediate impact
#J-18808-Ljbffr