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
Employment type
Job function
Industries
- Pharmaceutical Manufacturing, Biotechnology Research, and Technology, Information and Media