Manager, Quality Operations

LabConnect; Oregon; Hybrid; USD 90,000 - 130,000; Full time

Benefits offered by this job

Financial Security (Base Pay, 401k)

Health Benefits

PTO + Holidays

Disability & Life Insurance

Career growth opportunities

Job summary

LabConnect is seeking a Quality Assurance professional to champion quality initiatives, oversee CAPA processes, and coordinate audits across central lab operations. The role emphasizes regulatory compliance with CLIA, CAP, GCP, ICH, FDA, and EMA guidelines, while leading cross-functional teams to ensure data integrity and consistent quality across studies.

Ideal candidates will have 4+ years in lab quality roles, a life sciences degree, and familiarity with eQMS (Veeva) and document control.

Qualifications

• Bachelor's degree in life sciences, medical technology, or related field.
• Minimum 4 years of experience in a central lab or clinical trial lab, with at least 2 years in a quality management role.
• Professional quality certifications are optional.

Responsibilities

• Champion Quality initiatives aligned with global regulatory standards (CLIA, CAP, GCP, ICH, FDA, EMA).
• Assess and report on compliance with clinical trial protocols and regulatory guidelines.
• Manage and oversee Quality Events from issue identification through CAPA and effectiveness monitoring.
• Collaborate with lab operations, data management, and project teams to ensure quality in sample handling, testing, and reporting.
• Prepare for and facilitate sponsor audits and regulatory inspections.

Skills

CFRs & Guidelines

CLIA knowledge

GCP knowledge

CAP checklists

ICH guidelines

Quality management

Analytical skills

Communication

Leadership

Regulatory affairs

Education

Bachelor's degree in life sciences

Tools

eQMS (Veeva)

eLMS

Document control

MS Office

MS Project

Job description

OverviewLabConnect improves lives by partnering with pharmaceutical and biotech companies, and clinical research organizations (CROs) to accelerate the development of new medicines around the world.We are an independent, global, one-stop-shop focused on delivering Central Laboratory Services that are tailor-made, timely and flexible to meet the evolving study demands of traditional to increasingly complex trials. Additionally, we provide Functional Service Provider (FSP) Solutions, supporting our clients with scientific and technical expertise, acting as an extension of their team, coordinating all laboratory related needs, advising on strategies for lab data collection and providing end-to-end analytical and logistical solutions.

Essential Duties and Responsibilities

• Champion Quality initiatives, ensuring alignment with global regulatory standards and corporate excellence (e.g., CLIA, CAP, GCP, ICH, FDA, EMA).
• Assess and report on compliance with clinical trial protocols, sponsor requirements, and regulatory guidelines.
• Manage and oversee Quality Events from issue identification through investigation, containment, root cause analysis, correction, implementation of robust CAPA plans, and effectiveness monitoring.
• Partners with internal Quality Event action owners to manage all aspects of Quality Event activities, including gaining the commitment of cross-functional resources, scheduling Quality Event team meetings, and ensuring deliverables are met per project timelines.
• Perform timely, detailed Quality Event tasks, including assessing issue descriptions, reviewing Quality Event data sources, defining issues and impact assessments, and assisting with root cause analysis and quality problem solving.
• Ensure Quality Event and CAPA action plans are robust and executed promptly, with the appropriate sense of urgency.
• Work effectively with all levels of management to ensure Quality Event action plans can be supported and that the costs and resources needed to implement the plans are available.
• Train and mentor Quality Event owners in all required elements and best practices of Quality Event management, including containment, root cause analysis, correction, corrective and preventive actions, and effectiveness checks.
• Support vendor management activities related to quality issues, including issue resolution, CAPA follow-up, and effectiveness checks.
• Prepare for and facilitate sponsor audits, regulatory inspections (e.g., CLIA, CAP, FDA, EMA), and internal audits, and represent Quality Events during audits and Quality Event Review Board meetings.
• Coordinate timely and strategic resolution of audit findings and CAPAs, reinforcing a culture of accountability and continuous improvement.
• Collaborate with lab operations, data management, project teams, and others to ensure quality in sample handling, testing, and reporting.
• Review method validations, equipment qualifications, and laboratory investigations.
• Analyze quality monitoring data sources and apply statistical techniques to identify existing and potential causes of non-conformances.
• Perform periodic trend analysis and CAPA effectiveness measures for all quality system events and identify opportunities for improvement.
• Identify process inefficiencies and facilitate quality improvement initiatives across departments.
• Monitor and report quality KPIs (e.g., audit outcomes, deviation trends, CAPA effectiveness).
• Provide regular updates to leadership and contribute to strategic quality planning.
• Prepare training materials and conduct training for QMS topics.
• Collaborate with Human Resources regarding training program requirements affected by the QMS.
• Perform other tasks as defined by Quality Assurance Leadership.

Education and Experience

• Bachelor's degree in life sciences, medical technology, or related field.
• Minimum 4 years of experience in a central lab or clinical trial lab environment, with at least 2 years in a quality management role, or an equivalent combination of education and experience.
• Professional quality certifications are optional.

Skills and Ability

• Strong understanding of the CFRs, CLIA, CAP checklists, GCP, and ICH guidelines as they pertain to clinical trial operations.
• Strong understanding of the clinical laboratory and clinical trials environments.
• Excellent communication, leadership, analytical, organizational, and interpersonal skills.
• Ability to independently manage responsibilities and apply deep subject matter expertise to solve complex problems and guide decision making.
• Ability to read, analyze, and interpret technical procedures, professional journals, and governmental regulations, and to write reports, business correspondence, and procedures.
• Ability to effectively present information and respond to questions from groups of managers, clients, and auditors.
• Ability to apply concepts of basic algebra and statistics to quality data and trend analysis.
• Ability to solve practical problems and deal with a variety of concrete variables in situations where only limited standardization exists, and to interpret instructions furnished in written, oral, diagram, or schedule form.
• Working knowledge of Microsoft Office applications, including Word, Excel, PowerPoint, and Project. Experience with eQMS (e.g., Veeva), eLMS, document control, and other industry software preferred.

Supervisory Responsibilities

None

Physical Demands

While performing the duties of this job, the occupant is regularly required to:

• Prolonged periods of sitting at a desk and working on a computer.
• Prolonged use of computer and headphones for conference calls.
• Communicate effectively via phone, video, and email.
• Use hands and fingers to operate a computer and other office equipment.
• Sit 75% of the week.
• Stand 25% of the week.
• Walk and/or reach with hands and arms 15% of the week.
• Read text of various sizes.
• Communicate with others and hear.
• Lift, pull and/or push up to 25 pounds.

Work Environment

Office environment; noise level is usually moderate.

Travel Requirements

Travel Requirements: Minimal

Perks

• Financial Security (Base Pay, 401k Match and Possible Annual Bonus Eligibility)
• Health Benefits beginning on date of hire
• PTO plan, plus 11 Paid Company Holidays, and 1 Day to Volunteer in your community
• Short and Long-Term Disability, Life Insurance, and AD&D
• We celebrate our differences, which enriches our culture!

In addition to great perks and challenging work assignments, we invest in our people with career growth opportunities, globally.

We believe in a friendly and collaborative environment with open lines of communication. While living out our values of People First, Quality Focused, Customer Centered, Technology Driven, and Accountability Always .

We are proud to be an Equal Employment Opportunity Employer and value the diversity of our workforce.

We do not discriminate on the basis of race, gender, age, disability, religion, sexual orientation, or any other protected characteristic.

To learn more about equal employment opportunity, please view the posters here:LabConnect also prioritizes the privacy and security of your personal data. All candidate information is handled in accordance with General Data Protection Regulation (GDPR). To learn more, please review our Privacy Notice on our website, by navigating to