Technical Product Manager

Overview

Clario is hiring a Technical Product Manager (f/m/x) to drive innovative, data-driven products that improve patient outcomes and accelerate research. If you bring technical depth, product vision, and a passion for transforming healthcare through technology, this is your opportunity to make a meaningful impact.

What we offer

• Competitive compensation
• Attractive PTO plan
• Engaging employee programs

What you'll be doing

• Align product roadmaps with overall vision in partnership with Product Line Leaders and Upstream Product Managers
• Monitor emerging technologies and industry trends to inform strategy
• Develop and maintain multi-year release plans and initiatives
• Collaborate with technical teams on architecture, UX, and key capabilities
• Lead business architecture and workflows for assigned product areas
• Validate concepts and requirements through stakeholder feedback
• Balance priorities across architecture, maintenance, and new features
• Support agile ceremonies and team retrospectives
• Partner with Product Owners to ensure accurate knowledge transfer
• Act as subject matter expert in cross-functional initiatives
• Contribute to internal knowledge bases and user documentation
• Lead release readiness and commercial launch activities

What we look for

• Bachelor’s degree in business, science, technology, or medicine (Master’s in Business Administration preferred)
• 3+ years of product management experience, ideally in healthcare or clinical trials
• Strong technical acumen and ability to communicate across teams
• Full product lifecycle experience and domain knowledge in life sciences
• Proven collaboration with UX/UI teams on business and data workflows
• Excellent prioritization and decision-making in agile environments
• Strong customer engagement and communication skills
• Leadership experience with ability to influence across levels
• Experience with respiratory or clinical data capture technologies
• Experience developing specs within a Quality Management System
• Familiarity with FDA 510(k), CE Marking, and global device approvals
• Understanding of GCP, 21 CFR Part 11, device security, GMP, MDD, MDR

Seniority level

• Associate

Employment type

• Full-time

Job function

• Product Management

Industries

• Pharmaceutical Manufacturing, Biotechnology Research, and Technology, Information and Media