Molecular diagnostics product development experience
Medical device industry background
Regulated environment compliance (ivd/ivdr)
Danaher UK is seeking a Senior Program Manager for its Program Management Office at Cepheid, focusing on New Product Development in molecular diagnostics. The ideal candidate will have extensive experience in the medical device industry, particularly with IVD, and will be responsible for driving project execution excellence
Job Summary
The Senior Program Manager is responsible for leading New Product Development and Market Expansion projects in a molecular in-vitro diagnostic context to deliver products on time and within budget.
This role requires driving project execution excellence using best-practice methodologies embedded in the Danaher Business System while ensuring compliant IVD/IVDR design controls.
Cepheid offers comprehensive benefit programs including paid time off, medical/dental/vision insurance, and 401(k) to eligible employees alongside competitive compensation.
Matching Summary
Match Score: 85
Danaher UK is seeking a Senior Program Manager for its Program Management Office at Cepheid, focusing on New Product Development in molecular diagnostics. The ideal candidate will have extensive experience in the medical device industry, particularly with IVD, and will be responsible for driving project execution excellence.
Salary
Base: $150,000-$170,000; Bonus/Equity: Eligible for bonus/incentive pay; Benefits: Comprehensive package including PTO, medical/dental/vision, 401(k)
Skills & Requirements
Must-have
Molecular Diagnostics Product Development experience
Medical device industry background
Regulated environment compliance (IVD/IVDR)
Project execution excellence using DBS
Resource capacity planning and tracking
Nice-to-have
Danaher Business System Certified Practitioner status
PMP Certification
VPM or PSP certification
Culture change leadership
Global strategy translation skills
Key Requirements
Bachelor's Degree required, Master's preferred in Science or Engineering
Minimum five years of product development experience in medical device industry
Specific experience in Molecular Diagnostics Product Development
Track record of commercialization in US-IVD and CE-IVDR regulated environments