Job Description

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 ( ( 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

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