Manager - Quality Engineering

Job Description

Job Description

ABOUT US:
Biodesix is a leading diagnostic solutions company, driven to improve clinical care and outcomes for patients.

Biodesix Diagnostic Tests support clinical decisions to expedite personalized care and improve outcomes for patients with lung disease. 

Biodesix Development Services enable the world's leading biopharmaceutical, life sciences, and research institutions with scientific, technological, and operational capabilities that fuel the development of diagnostic tests, tools, and therapeutics.  

Our Mission: Transform patient care and improve outcomes through personalized diagnostics that are timely, accessible, and address immediate clinical needs.

Our Vision: A world where patient diseases are conquered with the guidance of personalized diagnostics.  

For more information, please visit

JOB LOCATION:

This role is based in Louisville, CO, and requires regular onsite collaboration. The team typically works onsite four days per week, particularly during onboarding, with flexibility based on business needs and performance. Candidates must reside within commuting distance. Travel is expected to be 10% or less.

THE ROLE:

The Manager - Quality Engineering will have broad and critical responsibilities that include: overseeing quality policies, procedures, processes, programs, and practices associated with product realization activities (including pre and post launch), and documentation to demonstrate conformance with appropriate standards and regulations; supporting product development teams in the design practices and risk and hazard management processes associated with development of medical devices, assays, and diagnostic test services per the Biodesix Quality Management System (QMS); managing the Quality Engineering group and accountable for applicable quality systems, including but not limited to Product Development, Change Control, Risk Management, Supplier Management, and Materials Management

WHAT YOU'LL DO:

Key Responsibilities 

• Day-to-day management, development, and implementation of quality assurance programs by the Company. 
• Deliver against Company goals to ensure core team projects are completed on time and meet the Company's quality standards. 
• Manage the Quality Engineering Team and associated systems and personnel 
• Strong collaboration with operations, managers, and product development staff. 
• Monitor production and purchasing services or activities to improve accuracy, customer service, or safety.  
• Development of validation plans for equipment, process, and devices.  
• With Operations and Development leadership, examine existing procedures or opportunities for streamlining activities to meet product improvement needs. 
• Contributor as the Quality function on verification & validation plans and reports. 
• Leading the development of the risk management plan(s) for product realization. 
• Assisting project teams on compliance with design requirements per CAP/CLIA, NYS CLEP and FDA QMSR, European MDR/IVDR, ISO 13485, ISO 14971, and other applicable ISO/EN standards as applicable to the Company. 
• Accountable for the following key functions within the Quality team Product Development Process: Design Control SOPs, Device Design History Files, Change Control, Risk Management, Quality/Process Improvement and Validation, Supplier and Material Management, Operational processes that impact quality 
• All other duties as assigned 

Management Responsibilities 

• Leads a team of employees  
• Sets team strategy, priorities, and performance expectations aligned to organizational goals 
• Drives talent development, succession planning, and workforce planning 
• Provides ongoing feedback and conducts performance evaluations 
• Promotes a culture of respect, collaboration, and belonging across the team and broader organization 

WHAT YOU'LL BRING:

• Knowledge and experience with (CAP/CLIA, NYS CLEP), ISO 13485, LDT, QMSR and Product Development. 
• Experience developing or reviewing product, equipment, or process verification and validation plans and reports.
• Clear understanding and experience implementing ISO 14971:2019 Risk Management into a QMS. 
• Previous experience in leading and participating in Product Development teams. 
• Previous experience in managing and growing teammates. 
• Working knowledge of developing equipment and/or process master validation plans. 
• Must be a team player with strong customer orientation and ability to work within a diverse disciplinary cross-functional team environment. 
• Strong verbal, written, organizational, time management and interpersonal skills. 
• Exercises judgment within broadly defined practices and policies in selecting methods, techniques, and evaluation criteria for obtaining results. 
• Must be able to communicate effectively in a verbal and written format. 
• The successful candidate will be: 
  • Able to perform all the required skills of this position with minimal direction. 
  • A detail oriented and quality minded individual with experience based good judgment. 
  • Strong computer skills, including working knowledge of MS Office and e-mail. 

WHAT YOU'LL GET:

• Annual Base Salary Range $100,000 – $116,000
• Discretionary Bonus opportunity 
• Comprehensive health coverage: Medical, Dental, and Vision 
• Insurance: Short/Long Term Disability and Life Insurance 
• Financial benefits: 401(k), Flex Spending Account 
• 120 hours of annual vacation 
• 72 hours of paid sick time off  
• 11 paid holidays + 3 floating holidays 
• Employee Assistance Program 
• Voluntary Benefits 
• Employee recognition program

WHAT TO EXPECT IN THE INTERVIEW PROCESS:

We want you to have a clear view of the Manager - Quality Engineering role—and we want to get to know the real you. Our interview process is designed to be thorough, transparent, and give you direct insight into what it's like to work here:

1. Virtual Recruiter Screen – A conversation to understand your background, what motivates you, and where you're looking to grow.
2. Hiring Manager Interview – A deeper discussion about your experience, skills, and approach.
3. Final On-Site Interview – Tour our corporate headquarters; interview with additional members of the team to discuss alignment and fit.

Biodesix is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status.