Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Adherence to all Good Manufacturing Practices (GMP) Safety Standards

Job Description

Position: Filtration Sr. Quality Manager

Location: Columbia, MO
Schedule: Typical M-F Days, some occasional weekend work

Division / Site Specific Information

This role is part of the site leadership team at Thermo Fisher Scientific and provides strategic quality leadership across manufacturing and operational functions. The Senior Manager of Quality partners closely with Operations, R&D, Commercial, and Customer teams to ensure consistent product excellence, regulatory compliance, and continuous improvement across the site.

Discover Impactful Work

As part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every day—enabling our customers to make the world healthier, cleaner, and safer.

As the Senior Manager of Quality, you will lead strategic quality initiatives while fostering a culture of continuous improvement and accountability. You’ll oversee quality management systems, drive inspection readiness, and elevate customer experience through strong quality standards. Your leadership will help ensure compliance with global regulatory requirements while supporting innovative solutions that advance science and improve lives.

A Day in the Life

Lead and manage Quality Assurance and Quality Control teams, providing coaching, development, and performance managementOversee site quality management systems to ensure compliance with GMP, ISO, FDA, and global regulatory requirementsDevelop and implement quality strategies aligned with business objectives and Thermo Fisher Scientific’s MissionDrive continuous improvement initiatives using Practical Process Improvement (PPI), risk-based methodologies, and data-driven decision-makingLead complex quality investigations, CAPA, and change control processesMaintain inspection readiness and serve as a key site representative during regulatory inspections and customer auditsPartner cross-functionally with Operations, R&D, Commercial, and Customer teams to enhance product quality and customer satisfactionAnalyze quality metrics and trends to identify risks, opportunities, and system improvementsBuild strong customer relationships by ensuring consistent product quality and responsiveness

Keys to Success

Education

Advanced Degree with a minimum of 5 years of experience ORBachelor’s Degree with a minimum of 8 years of experiencePreferred fields of study: Science, Engineering, Chemistry, or related technical disciplineProfessional certifications preferred (ASQ, Lean Six Sigma, or equivalent)

Experience

Experience in pharmaceutical, medical device, or regulated life sciences environmentsMinimum of 3 years of people leadership or quality management experienceDemonstrated experience leading quality investigations, CAPA, and change control activitiesProven experience implementing continuous improvement initiativesExperience hosting and managing regulatory inspections and customer auditsExperience partnering cross-functionally at senior leadership levels

Knowledge

Expert understanding of global quality standards including ISO 13485, ISO 9001, FDA 21 CFR 820, and EU MDR/IVDRStrong knowledge of GMP requirements and quality management systems

Skills

Strong project management and cross-functional leadership skillsAdvanced problem-solving, risk assessment, and root cause analysis capabilitiesProficiency with quality management systems and data analysis toolsExcellent written and verbal communication skills

Abilities

Ability to influence and build collaborative relationships at all organizational levelsAbility to lead teams through change and continuous improvement initiativesAbility to travel up to 25% as required

Other

Must be legally authorized to work in the United States without sponsorship, now or in the futureMust be able to pass a comprehensive background check, including a drug screening