Thermo Fisher

QC Supervisor Nights

Lebanon, Tennessee, USA Full time

Work Schedule

Third Shift (Nights)

Environmental Conditions

Cleanroom: no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair etc... allowed

Job Description

  • Responsibilities
    • Coordinate daily quality control activities in accordance with design and process documentation to meet safety, quality, output, on-time delivery targets and revenue activities are completed
    • Participate and lead improvement events (such as Kaizen, 5S, Practical Process Improvement); coach and mentor direct reports to drive continuous improvement as a way of life
    • Partner with the Operations team to facilitate understanding of quality expectations and requirements
    • Lead daily quality control meetings and create and publish daily/weekly/monthly metrics
    • Lead training and coaching of direct reports and complete annual performance reviews
    • Ensure adherence to company policies and procedures, holding staff accountable and working with human resources to apply corrective action as required
    • Identify quality constraints and resolve issues, including resolving material concerns, prioritizing support functions (receiving, inspection, mfg. engineering, etc.) and escalating issues
    • Execution of root cause correction plan on any metrics not meeting target
    • Ensure that safe work practices are in use, including team’s adherence to Personal Protective Equipment (PPE) requirements of the job function
    • Assist with 3rd party audits
    • Direct the daily workload to ensure schedule completion while managing utilization and efficiency
    • Build and develop a disciplined workforce that adheres to all procedures and Work Instruction Documents
    • Ability to have flexible work schedule and cover shifts as needed. Weekday and Weekend shifts
    • Assist in TrackWise investigation and Root Cause investigation.

  • How will you get here?
    • High School Diploma or GED, bachelor’s degree from an accredited University preferred
    • Minimum 3 years’ experience leading teams
    • Experience working in a regulated environment (medical device or pharmaceutical preferred)

  • Knowledge, Skills, Abilities
    • 3-years’ experience leading a team in a professional work environment
    • Working knowledge of Microsoft Office (Word, PowerPoint, Excel,)
    • Problem solving skills
    • Written and verbal communication skills
    • Ability to coordinate and work on multiple projects with other departments or functions
    • Ability to mentor, train, motivate, and coach
    • Preferred experience working in a ISO9001, ISO16949 or ISO13485 environment.
    • Preferred experience with Continuous Improvement, Lean Manufacturing, and/or Six Sigma experience