Work Schedule
Standard (Mon-Fri)

Environmental Conditions
Office

Job Description

Job Description

At Thermo Fisher Scientific, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on - now and in the future.

• Lead and facilitate Kaizens and Projects
• Diplomatically cultivate an action-biased culture of continuous improvement to improve Quality, Productivity and Customer Allegiance
• Coach the teams Lean Management System (tiered daily management systems, Gemba walks, and leader standard work) and other coaching tools to transform the culture
• Identify areas of opportunity for improvement/growth and support teams on implementation of these opportunities
• Provides PPI Business System program support through project traceability, pipeline building and productivity tracking and reporting
• Partner with Finance personnel to evaluate project savings estimates, validate reported PPI benefits, and ensure accurate accounting of PPI Productivity
• Improve decision-making models and problem-solving capabilities within the teams to increase autonomy and the pace of change
• Regularly seek feedback from Division / BU / Function staff to directly meet and understand their needs

• Bachelor's degree in engineering, manufacturing, pharmaceuticals, biological science or related field.
• Advanced degree preferred

• 5+ years of experience in engineering, manufacturing, clinical, pharmaceuticals, biological, and/or GMP environment (QA, QC, manufacturing), or combination of
• "Hands-on" track record of leading teams directly or indirectly to achieve results

• Strong interpersonal skills and the ability to connect with and positively influence all levels of the organization
• Excellent skills in Microsoft Office suite; Word, Excel, Project, Visio, Outlook and PowerPoint.
• Proven track record to drive cross functional teams to solve problems and implement sustainable improvements within the organization
• Catalyst to drive continuous improvement in both non-operational and operational areas
• Self-Starter and independent
• Passion and enthusiasm for driving improvement and leading change
• Excellent Financial Acumen
• Demonstrated project management experience in a fast-paced environment
• Strong analytical skills, attention to detail and ability to multi-task
• Ability to interface and effectively influence all levels of the organization.
• Superior communication skills, verbal and written; proficiency with English language
• Ability to travel regionally and globally up to 25% on an annual basis

• Able to communicate, receive, and understand information and ideas with diverse groups of people in a comprehensible and reasonable manner.
• Able to work upright and stationary and/or standing for typical working hours.
• Able to lift and move objects up to 25 pounds.
• Able to work in non-traditional work environments.
• Able to use and learn standard office equipment and technology with proficiency.
• May have exposure to potentially hazardous elements, including infectious agents, typically found in healthcare or laboratory environments.
• Able to perform successfully under pressure while prioritizing and handling multiple projects or activities.