QC Supervisor Nights at Thermo Fisher Scientific

Lebanon, Tennessee, United States

Thermo Fisher Scientific Logo
Not SpecifiedCompensation
Mid-level (3 to 4 years)Experience Level
Full TimeJob Type
UnknownVisa
Manufacturing, Life Sciences, Medical DevicesIndustries

Requirements

  • 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)
  • 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 an ISO9001, ISO16949 or ISO13485 environment
  • Preferred experience with Continuous Improvement, Lean Manufacturing, and/or Six Sigma

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
  • Participate and lead improvement events (such as Kaizen, 5S, Practical Process Improvement); coach and mentor direct reports to drive continuous improvement
  • 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
  • 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

Skills

Key technologies and capabilities for this role

Quality ControlKaizen5SRoot Cause AnalysisTrackWiseTeam LeadershipPerformance ReviewsContinuous ImprovementPPEAudits

Questions & Answers

Common questions about this position

What education and experience are required for the QC Supervisor Nights role?

A High School Diploma or GED is required, with a bachelor’s degree preferred. Minimum 3 years’ experience leading teams is needed, preferably in a regulated environment like medical device or pharmaceutical.

What is the work schedule for this position?

This is a full-time third shift (nights) role in a cleanroom environment with restrictions on hair products, jewelry, makeup, etc. Flexible work schedule is required, including ability to cover weekday and weekend shifts as needed.

What key skills are needed for this QC Supervisor position?

Key skills include 3 years’ experience leading a team, working knowledge of Microsoft Office (Word, PowerPoint, Excel), problem-solving skills, written and verbal communication skills, and ability to coordinate multiple projects.

What does the company culture emphasize in this role?

The role emphasizes continuous improvement as a way of life through events like Kaizen, 5S, and Practical Process Improvement, building a disciplined workforce that adheres to procedures, and ensuring safe work practices with PPE.

What makes a strong candidate for the QC Supervisor Nights job?

Strong candidates have experience in regulated environments (medical device or pharmaceutical), preferred ISO9001/ISO13485 experience, and Continuous Improvement/Lean Manufacturing/Six Sigma background, along with team leadership skills.

Thermo Fisher Scientific

Provides life sciences products and services

About Thermo Fisher Scientific

Thermo Fisher Scientific offers a variety of products and services that support scientific research and healthcare, including laboratory equipment, reagents, and software solutions. Their products are used in applications like protein biology, real-time PCR, and sequencing, serving clients such as academic institutions and pharmaceutical companies. Unlike competitors, Thermo Fisher emphasizes customer support and education, helping clients optimize their experiments. The company's goal is to be a leading provider of life sciences solutions that contribute to a healthier and safer world.

Waltham, MassachusettsHeadquarters
1956Year Founded
$17MTotal Funding
IPOCompany Stage
Biotechnology, HealthcareIndustries
10,001+Employees

Risks

Increased competition in single-use bioprocessing may impact market share.
Sale of anatomical pathology business could create a temporary product gap.
Investment in miDiagnostics may face regulatory challenges affecting returns.

Differentiation

Thermo Fisher offers a comprehensive range of life sciences products and services.
Their well-known brands include Thermo Scientific, Applied Biosystems, and Invitrogen.
They provide strong customer support and educational resources to optimize client workflows.

Upsides

Expansion of biologics production facility enhances capacity for precision biologics monitoring.
Investment in miDiagnostics aligns with demand for rapid diagnostic solutions in BioPharma.
Collaboration with Mainz Biomed positions them in the growing cancer detection market.

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