Head of Programme Management

CorDx a multi-national biotech organization focused on pushing the limits of innovation and supply in global health. With over 2,100 employees across the world, serving millions of users in over 100 countries, CorDx delivers rapid testing and point-of-care medical device solutions used in the detection of infectious diseases such as COVID-19, pregnancy, drugs of abuse, biomarkers, and more. CorDx is at the cutting edge of technology, artificial intelligence, and data science with the goal of delivering diagnostic solutions to some of the most critical questions in healthcare.

Job Type: Full time

This role will oversee complex product development initiatives from concept through commercialization, ensuring alignment with strategic objectives, regulatory compliance, and time/cost constraints. The ideal candidate will have a strong background in project/program management, deep understanding of the biotech/IVD landscape, and a proven track record in delivering results through collaboration and leadership.

Lead cross-functional program teams across R&D, Regulatory Affairs, Clinical, Quality, Operations, and Commercial to deliver IVD/diagnostic products from feasibility to launch.

Develop and manage detailed program plans, timelines, budgets, and resource allocation.

Serve as the primary point of contact for program status, risk assessment, and issue resolution.

Track key milestones and prepare executive-level reporting on program performance and progress.

Ensure programs meet regulatory requirements (e.g., Manage program governance, including steering committee meetings and stage gate reviews.

Identify risks and proactively implement mitigation strategies to ensure timelines and deliverables are met.

Bachelor’s degree in Life Sciences, Engineering, or a related field; advanced degree (MS, PhD, or MBA) preferred.

• 8-10+ years of experience in the biotech, diagnostics, or medical device industry, with a focus on IVD product development.
• 5+ years of program/project management experience in a regulated environment.
• Strong knowledge of regulatory pathways, quality systems (e.g., Proven ability to lead cross-functional teams and manage complex programs with multiple stakeholders.
• PMP certification or formal training in project/program management strongly preferred.
• Experience with global product launches and managing distributed teams.

Familiarity with Agile and/or Stage-Gate development methodologies.

Prior experience working with external partners and managing outsourced development/manufacturing.

Comprehensive medical, dental, and vision insurance.

• Flexible paid time off (PTO) policy.
• Equal Opportunity Statement: We are an equal opportunity employer committed to inclusion and diversity. We do not discriminate based on race, gender, religion, sexual orientation, age, color, marital status, veteran status, disability status, national origin, or any other protected characteristic.