Thermo Fisher Scientific Sr. Quality Engineer in Lenexa, Kansas
Senior Quality Engineer - Lenexa, KS
Our team in Lenexa, KS is at the heart of the global response to COVID-19. Given the significant demand for COVID-19 testing, Thermo Fisher is expanding our capacity in Lenexa with a new $40 million facility dedicated to viral transport media (VTM) for COVID-19 sample collection. We are hiring more than 300 new team members to join us in this effort.
The Sr. Quality Engineer will lead in the implementation of quality assurances practices, process controls, change control and Corrective and Preventive Action activities. This position is embedded in the Operations Work Stream. The Sr. Quality Engineer will partner with Operations and is the primary point of contact for all Quality decisions affecting daily activities.
The Sr. Quality Engineer will approve investigations, deviations, change controls, validation protocols, validation reports, Operations SOP's, and in-process controls. In addition they will evaluate and recommend process changes to improve the Value Stream performance and regulatory compliance.
The Sr. Quality Engineer is responsible for managing, and further developing Validation personnel and for organizing their work to be in alignment (or support) of the site Quality goals. The individual selected for this role will act as an effective leader in promoting quality disciplines, decisions and practices and will apply sound, systematic, problem-solving methodologies in identifying, prioritizing, communicating and resolving quality issues.
Full-Time Employment Opportunities - Complete with full medical/dental benefits and more
Redesigned/Expanded site - Refresh of existing site + a nearby new facility
Interested? We are growing and want you to grow with us! Join us today! Check out our site and hear from some of our team members .
What will you do?
Provide Quality review and approval of all investigations, deviations, change controls, validation protocols, validation reports, SOP's, and in-process controls in support of the assigned Value Stream.
Enable collaborative relationships between Operations and Quality with the overall focus of improving customer satisfaction.
Troubleshoot process issues. Lead inter-department teams in the resolution of process issues and quality problems.
Work as a member of new product introduction teams to provide quality input and capability analysis.
Work closely with Operations, R & D, Purchasing and Engineering to improve quality while reducing material scrap and costs.
Champion continuous improvement and the transition to a Lean Manufacturing Environment.
Drive quality management focus on productivity improvements throughout the business unit.
Work effectively as a member of cross-functional teams.
Partner with Operations leadership to establish controls and inspection points to facilitate detection, correction, and prevention of nonconforming materials, parts, assemblies, and products.
Drive Customer complaints to resolution; Serve as Quality Representative for all quality-related corrective/preventive actions within the Value Stream.
Assure that quality standards comply with division and departmental policies, national and international codes, and applicable safety requirements.
Leads PPI activities at the site including the facilitation of Kaizen events. Supports Operations and Quality team members on process improvement activities.
Analyze trends and collaborates with manufacturing to investigate trends, conduct root cause analysis and lead corrective actions for processes and products.
Manage Validation personnel reporting to the position to effectively develop, recruit, train, evaluate, motivate, delegate and monitor their work as it relates to the assigned value stream and Quality goals.
How will you get here?
Bachelor's Degree in a science, engineering or related field
5 years of experience in a regulated environment such as medical device, pharmaceutical, biotechnology or clinical
Bachelors of Science Degree in Biology or Microbiology
6 or more years of experience in a regulated environment such as medical device, pharmaceutical, biotechnology or clinical
Strong working knowledge of quality related tools, such as structured problem solving, FMEA (Failure Mode and Effects Analysis), SPC (Statistical Process Control), DOE (Design of Experiments) and Six Sigma
Previous Supervision or Management experience
Strong background in process control and statistical techniques
Medical device, GMP, EU Regulation or ISO 13485 background
Demonstrated working knowledge of compliance, quality and scientific principles
Must be a self-starter who can take general concepts and direction and produce desirable results
Ability to prioritize multiple tasks function effectively in a global, multi-site organization
Demonstrated ability to work effectively as a member of a cross-functional team
Strong working knowledge of various computer software, such as Mini-tab
Experience with lean manufacturing practices. Green Belt or Black Belt certification a plus
Knowledge of qualification / validation (process, sterilization, software) requirements
Perform independently without continual direction and exercise considerable latitude in determining technical objectives and solutions to complex problems.
Excellent oral and written communication skills
Strong leadership skills with the ability to challenge, influence, and build consensus.
Ability to work both independently and as a team member.
Strong business acumen.
At Thermo Fisher Scientific, each one of our 75,000 extraordinary minds has a unique story to tell. Join us and contribute to our singular mission-enabling our customers to make the world healthier, cleaner and safer.
Thermo Fisher Scientific is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, creed, religion, color, national or ethnic origin, citizenship, sex, sexual orientation, gender identity and expression, genetic information, veteran status, age or disability status.