Quality Manager - Operations Execution & Performance

Thermo Fisher Scientific • Marietta, OH

4d • Onsite

About The Position

As a Quality Manager - Operations Execution and Performance at Thermo Fisher Scientific, you will contribute to excellence across our quality management systems while enabling our mission to make the world healthier, cleaner and safer. You will work as a tactical team member within the Quality group to drive business objectives into daily work. You will guide quality initiatives, support continuous improvement, and cultivate a culture of compliance and operational excellence. You will work collaboratively across functions, ensuring adherence to regulatory requirements while maintaining the highest quality standards for our products and services. You will assign daily work to team members and ensure KPIs and timelines are being met.

Requirements

• Minimum Bachelor's Degree (Preferred Fields of Study: Mechanical or Industrial Engineering or related scientific/technical field)
• 8 years of operations experience
• 3-5 years of leadership/management experience
• Experience participating in internal/external audits and regulatory inspections
• Experience with continuous improvement methodologies (Lean, Six Sigma)
• Successful experience implementing and improving quality systems
• Manage KPIs and order timelines
• Comprehensive knowledge of quality management systems and regulations (ISO 9001, ISO 13485, FDA)
• Strong understanding of quality tools and methodologies (CAPA, risk analysis, FMEA, root cause analysis)
• Ability to maintain organization within fast paced environment.
• Demonstrated ability to develop and mentor quality teams
• Skill in cross-functional collaboration and stakeholder management
• Strong analytical and problem-solving capabilities
• Clear written and verbal communication skills
• Proficiency with quality management software (TrackWise, Document Control Systems)
• Ability to promote quality culture across all levels
• Focus on customer needs and ability to manage customer/supplier relationships
• Must be legally authorized to work in the United States without sponsorship.
• Must be able to pass a comprehensive background check, which includes a drug screening.

Nice To Haves

• Lead Auditor certification in ISO 13485/9001 preferred
• Experience in pharmaceutical, medical device, or regulated life sciences industry preferred
• Project management experience preferred

Responsibilities

• Drive business objectives into daily work.
• Guide quality initiatives.
• Support continuous improvement.
• Cultivate a culture of compliance and operational excellence.
• Work collaboratively across functions.
• Ensure adherence to regulatory requirements while maintaining the highest quality standards for our products and services.
• Assign daily work to team members and ensure KPIs and timelines are being met.

Benefits

• Competitive compensation
• Annual incentive plan bonus
• Healthcare
• Range of employee benefits
• Innovative, forward-thinking organization
• Outstanding career and development prospects
• Exciting company culture that stands for integrity, intensity, involvement, and innovation

What This Job Offers

• Job Type: Full-time
• Career Level: Manager