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Supplier Relations Specialist
Danaher Corporation. Serve as a liaison between CCOE, cross-OpCo teams, and external clinical suppliers .
Posted 10/28/2026full-timeRemote • California • United StatesMid-LevelSenior💰 $95,000 - $105,000 per yearWebsite
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in contract negotiation, supplier management, and regulatory compliance within clinical studies. Proficient in applying Danaher Business System tools for process improvement and maintaining effective communication across cross-functional teams.
Highest-signal resume keywords
Contract Negotiation SkillsSupplier ManagementGCP KnowledgeBudgeting ExperienceMicrosoft Office Proficiency
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Contract NegotiationSupplier ManagementBudgetingGCP KnowledgeSOP Knowledge
Soft Skills
Proactive Team PlayerCollaborative ApproachClear Communication
Tools & Technologies
Microsoft ExcelMicrosoft WordMicrosoft PowerPoint
Industry Keywords
Regulated EnvironmentClinical StudiesMedical DevicePharmaceuticalFinance
Tech Stack
Tools & technologiesGoogle Cloud Platform
About the role
Key responsibilities & impact- Serve as a liaison between CCOE, cross-OpCo teams, and external clinical suppliers
- Coordinate supplier setup, purchase orders, payments, performance documentation, and ongoing process support
- Support contract workflow activities, including routing, tracking, documentation, stakeholder follow-up, and coordination with CCOE, OpCo teams, Legal, Procurement, and external suppliers
- Maintain clear communication, documentation, and alignment across supplier-related activities
- Apply Danaher Business System tools and standard work to support process consistency and continuous improvement
- Collaborate globally with EU and US teams to ensure timely delivery and support
- Maintain knowledge of GCP, global standards, and SOPs to ensure regulatory adherence for clinical studies
Requirements
What you’ll need- Bachelor’s degree in scientific, finance, biological, or medical science field with 5+ years of experience in a regulated environment, or another relevant degree with 8+ years of the same experience
- Strong contract negotiation skills with a track record of successful contract negotiations
- Thorough budgeting experience with relevant stakeholders from the clinical environment
- Strong understanding of supplier management
- Proficiency in Microsoft Office, including Excel, Word, and PowerPoint
- Proactive team player with a collaborative approach and interest in building and maintaining supplier processes
- Knowledge of GCP, global standards, and SOPs for clinical studies
- Previous experience in medical device, pharmaceutical, finance, or other highly regulated industries is a plus
Benefits
Comp & perks- Bonus/incentive pay eligibility
- Paid time off
- Medical, dental, and vision insurance
- 401(k)
- Flexible, remote working arrangements for eligible roles
- Remote work from home
- Reasonable accommodations for applicants and employees with disabilities