VP, Laboratory Testing and Biotherapies Quality Services
At Vitalant, the impact you make doing work that is purposeful, meaningful, and worthwhile is vital. As a member of our non-profit organization, you can be impact-inspired to provide vital clinical services to communities nationwide, vital products to those in need of a donor's generosity, or vital scientific research that advances blood safety worldwide.
Work Shift (if applicable):
Shift 1 (United States of America)Job Description:
At Vitalant, our mission is to save and improve lives through blood donation, transplantation, cellular therapies, research, and innovation. As the VP, Laboratory Testing and Biotherapies Quality Services, you will play a critical leadership role in advancing that mission by providing enterprise-wide strategic oversight for quality and operational excellence across laboratory testing, clinical apheresis, cell processing, and biomanufacturing operations. This executive leader is responsible for strengthening Vitalant’s enterprise quality system, ensuring compliance with regulatory and accreditation requirements, and partnering with organizational leaders to drive performance, mitigate risk, support growth, and enhance patient and customer outcomes. The role also leads and develops high-performing quality teams while fostering a culture of accountability, continuous improvement, and service excellence aligned with Vitalant’s RITE values of Respect, Integrity, Teamwork, and Excellence.
Compensation: $208,270.40 - $260,000.00
This hybrid position is based in Scottsdale, AZ and requires working onsite three days per week and from a home office two days per week.
Applications accepted through July 24, 2026
Our comprehensive total rewards support you, your family, and your future with:
Medical, dental, and vision insurance
401K + 5% company match
Tuition assistance up to $5k per year
Free basic life and AD&D insurance
Free short-and-long-term disability insurance
Paid time off
Employee Resource Groups
Recognition and perks
As the VP, Laboratory Testing and Biotherapies Quality Services, you'll get to:
Provide executive leadership for enterprise quality strategy, governance, and operational excellence across laboratory testing, clinical apheresis, cell processing, and biomanufacturing operations.
Lead and continuously enhance the enterprise quality system to ensure regulatory compliance, risk mitigation, inspection readiness, and sustained performance improvement.
Serve as a strategic advisor to executive leadership on quality, regulatory, and compliance matters, including emerging risks, quality system effectiveness, and business impact.
Ensure compliance with applicable regulatory, accreditation, and industry standards, including FDA, CLIA, FACT, ASHI, CAP, The Joint Commission, and AABB requirements.
Partner with senior leaders to align quality initiatives with organizational goals, operational performance, customer expectations, and growth strategies.
Oversee enterprise quality metrics, audits, data analytics, and trend monitoring to identify risks, drive informed decision-making, and improve outcomes.
Sponsor corrective and preventive action programs and continuous improvement initiatives to strengthen quality performance and operational effectiveness.
Provide executive oversight for the evaluation and disposition of nonconforming products, processes, and test results, including regulatory reporting and customer communications when required.
Represent Vitalant with regulatory agencies, accrediting organizations, customers, and external partners, ensuring successful inspections, audits, and reviews.
Influence enterprise decisions related to processes, technologies, systems, equipment, and quality monitoring practices to support compliant, scalable, and efficient operations.
Lead, mentor, and develop a high-performing team of quality professionals while fostering a culture of accountability, collaboration, and continuous improvement.
Manage departmental goals, performance metrics, budgets, and resource planning to support enterprise quality, operational, and financial objectives.
Monitor industry trends, regulatory developments, and emerging best practices to strengthen organizational capabilities and support long-term success.
REQUIREMENTS:
KNOWLEDGE/EDUCATION
Bachelor’s degree in healthcare administration, life sciences, laboratory science, quality management, business administration, or a related field required. Equivalent combination of education and relevant senior-level experience may be considered.
Master’s or advanced degree in business, healthcare administration, quality management, laboratory science, life sciences, or a related field preferred.
Advanced knowledge of quality systems, regulatory requirements, accreditation standards, risk management, and operational compliance within FDA-regulated, laboratory, transfusion medicine, clinical apheresis, cell therapy, biomanufacturing, or related healthcare environments required.
Knowledge of applicable federal, state, local, accreditation, and industry standards, including FDA, CLIA, FACT, ASHI, CAP, The Joint Commission, AABB, and other applicable regulatory or accrediting bodies required.
Knowledge of enterprise quality governance, audit programs, corrective and preventive action, inspection readiness, quality metrics, data analytics, and continuous improvement methodologies required.
Knowledge of technology-enabled quality systems, laboratory information systems, computerized system validation, software implementation, and system life cycle methodology preferred.
LICENSES/CERTIFICATIONS
Certification in quality, regulatory affairs, project management, or process improvement preferred, such as Certified Manager of Quality/Organizational Excellence (CMQ/OE), Certified Quality Auditor (CQA), Regulatory Affairs Quality (RAQ) certification, Project Management Professional (PMP), Lean Six Sigma, or equivalent credential.
Professional certification or licensure in a relevant clinical, laboratory, transfusion medicine, histocompatibility, cell therapy, biotherapies, or healthcare discipline preferred, such as Medical Laboratory Scientist/Medical Technologist, Specialist in Blood Banking (SBB), Certified Histocompatibility Specialist (CHS), Certified Advanced Biotherapies Professional (CABP), Registered Nurse (RN), or equivalent credential.
Maintenance of applicable professional certification, licensure, or continuing education requirements, where held, is expected.
EXPERIENCE
Ten years of related experience in a regulated industry required. To include:
Six years of operational or quality leadership experience in an FDA regulated organization.
Two years of experience in quality, regulatory, and/or auditing leadership role at the director level or higher with an FDA regulated organization.
Five years of experience in clinical leadership role (laboratory, nursing, etc.) preferred.
Previous experience supporting a multi-location environment preferred
SKILLS/ABILITIES
Must possess the skills and abilities to successfully perform all assigned duties and responsibilities.
Demonstrated ability to provide enterprise leadership, set strategic direction, and influence executive and operational decision-making across complex, regulated environments.
Ability to organize, prioritize, and execute a variable workload and multiple enterprise priorities in a fast-paced, matrixed environment.
Ability to build trusted relationships and work effectively with executive leadership, operational leaders, quality partners, regulatory agencies, customers, and external stakeholders.
Effective executive-level oral and written communication skills, including the ability to translate complex regulatory, quality, operational, and financial information into clear guidance and actionable recommendations.
Ability to think strategically, synthesize complex business, quality, compliance, and financial data, and develop practical, innovative, and sustainable solutions.
Demonstrated ability to lead, develop, coach, and motivate leaders and professionals; establish accountability; and foster collaboration, engagement, and continuous improvement.
Must possess sound judgment, decisiveness, integrity, discretion, and the ability to maintain confidentiality regarding sensitive organizational, regulatory, employee, customer, and business information.
Ability to lead through ambiguity, change, and competing priorities while maintaining focus on compliance, quality, service, and organizational outcomes.
Proficient technology skills, including the ability to use business, quality, and data systems to support decision-making, reporting, and operational oversight.
Location:
9305 East Via de Ventura
Scottsdale, AZ 85258
Job Category:
Leadership OperationsContact Information: careers@vitalant.org
If you are impact-inspired to help others, and making a difference is vital for you, you'll experience a career built on purpose, a company created to care, and a team committed to lead - together.