Onsite Program Manager Jobs in Oregon (NOW HIRING)

POSITION SUMMARY:

The Program Manager will lead cross-functional programs supporting product development initiatives at the Boulder, CO site. Projects and programs may include development, validation, and regulatory submission of diagnostic products; support of biopharma companion diagnostic (CDx) partnerships; and product sustainment and lifecycle management efforts. This role is responsible for driving execution across product development cross functional teams, including R&D, software, manufacturing, laboratory operations, quality, regulatory, clinical development, commercial, alliance management, and external partners, to ensure timely, compliant delivery of key milestones and contractual commitments.

The Program Manager will partner with functional leaders and stakeholders to translate product strategy into executable plans, manage cross-functional dependencies, and maintain alignment across internal and external stakeholders. This role requires strong program management fundamentals, experience and comfort operating in regulated environments, and the ability to coordinate complex, multi-disciplinary efforts simultaneously. The Program Manager will drive, communicate, and engage all project partners to enable accountability, problem solving, and on-time/within-budget delivery for simultaneous projects and programs. Success in this role requires onsite engagement (up to 25% travel) to facilitate rapid decision-making, build alignment, and resolve issues in a highly collaborative, fast-paced setting. This position reports to the Associate Director of Program Management.

PRIMARY RESPONSIBILITIES:

• Drive end-to-end execution of product development programs, including planning, scheduling, resource coordination, and risk management across assay, software, and systems development, ensuring alignment with regulatory and business requirements.

• Support regulatory product development activities, ensuring alignment with regulated processes and quality systems, including design control processes (ISO 13485), software lifecycle standards (IEC 62304), change management, and quality system requirements (FDA, CAP/CLIA), including documentation and traceability of requirements and deliverables.

• Coordinate regulatory submission readiness, including support for Investigational Device Exemptions (IDEs), pre-submissions, and other global regulatory filings.

• Lead cross-functional alignment across R&D, software, regulatory, quality, and clinical teams to ensure clear requirements, priorities, and deliverables.

• Translate product strategy into actionable program roadmaps, including timelines, milestones, and interdependencies, ensuring alignment with organizational priorities and securing stakeholder buy-in.

• Extract and refine user needs and requirements from stakeholders and lead teams to focus on the most valuable deliverables.

• Partner with Alliance Management to manage external biopharma and CDx partnerships, coordinating joint program plans, deliverables, timelines, and communication across organizations.

• Adhere to formal governance processes to communicate program status, risks, and trade-offs; escalate issues as needed; and present data-driven recommendations and business proposals to senior leadership to enable timely, informed decision-making.

• Identify, track and manage program risks and dependencies, proactively identifying mitigation strategies and driving issue resolution.

• Drive cross-functional accountability, influencing without direct authority to ensure alignment, ownership, and timely execution.

• Support continuous improvement of product development processes, tools, and cross-functional ways of working.

• Cultivate, build and maintain positive and collaborative relationships with cross-functional teams.

QUALIFICATIONS:

• 3-5+ years of experience in program management, or equivalent combination of project management and relevant functional experience in biotechnology, diagnostics, clinical laboratory, or life sciences.

• Experience supporting product development in regulated environments (IVD, medical device, or similar).

KNOWLEDGE, SKILLS, AND ABILITIES:

• Background in NGS diagnostics, including assay and software components (MRD experience preferred).

• Strong familiarity with design controls (ISO 13485) and software lifecycle processes (IEC 62304).

• Experience supporting regulatory submissions (e.g., IDE, 510(k), PMA, or equivalent) preferred.

• Exposure to clinical trial operations and execution (preferred).

• Experience working with external partners, such as biopharma or CDx collaborations (preferred).

• PMP or equivalent certification preferred.

• Ability to influence senior stakeholders and drive alignment in matrixed organizations.

• Strong organizational and program management skills, with the ability to manage multiple concurrent initiatives.

• Analytical mindset with strong attention to detail and ability to identify risks and dependencies.

• Excellent executive communication skills, with the ability to tailor messaging across technical and non-technical audiences.

• Proficiency with program management and collaboration tools (e.g., Smartsheets, JIRA, Office Timeline, etc.).

• Situational awareness, coupled with facilitation, problem solving, and conflict resolution skills to drive cross-functional decision-making.

• This position may be required to work across time zones as needed to support project schedules.