Technical Program Manager - Product Development
BioTalent
Technical Program Manager - Product Development (Molecular Diagnostics) Summary An innovative genomics and molecular diagnostics organization is seeking a Technical Program Manager to lead cross-functional execution of a next-generation diagnostic platform from concept through commercial launch. This role partners closely with engineering, assay development, software, operations, regulatory, and quality teams to drive planning, prioritization, and milestone delivery across a complex product development lifecycle. Ideal for a program leader experienced in IVD environments and phase-gate development frameworks.
Responsibilities
Responsibilities
- Lead cross-functional program planning, scheduling, and execution across platform development activities
- Facilitate core team meetings, design reviews, and executive program updates
- Develop and maintain integrated program schedules including dependencies, critical path, and resource constraints
- Drive cross-discipline resource alignment and prioritization discussions
- Administer stage-gate product development processes and ensure timely completion of phase deliverables
- Identify program risks and implement mitigation strategies with functional stakeholders
- Track milestones and communicate program status to leadership
- Coordinate design verification, design transfer, and regulatory submission readiness activities
- Enable efficient decision-making through structured stakeholder communication
- Improve program management tools, templates, and operating processes
- 6-8+ years of experience in technical program or project management supporting full product development lifecycles
- Strong experience operating within stage-gate / phase-gate environments
- Demonstrated success managing complex, multi-workstream technical programs
- Expertise in schedule development, resource planning, risk management, and critical path tracking
- Strong facilitation and stakeholder alignment skills across technical teams
- Experience with program management tools (MS Project, Smartsheet, Jira, or similar)
- Experience supporting IVD product development
- Familiarity with FDA 510(k), ISO 13485, and design controls preferred
- Technical fluency in molecular diagnostics or adjacent life sciences technologies
- PMP or equivalent certification a plus
- B.S. or M.S. in Engineering, Life Sciences, or related technical fiel
Vacancy posted 1 day ago
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