Jobs · Engineering · Missouri

Quality Control Manager

ZEISS Group · Chesterfield, MO · 1 mo ago
On-siteEngineeringFull-time

About the role

Lead a department in a medical device manufacturing environment and ensure the highest level of production quality, efficiency, and output.

Responsibilities

  • Direct leadership of the site operational QC employees
  • Assure that quality inspectors are well trained in support of their career development paths and the company's growth plans
  • Manage and supervise QC laboratory activities and equipment
  • Use effective negotiation skills to drive alignment and resolve conflict
  • Provide coaching and constructive feedback
  • Collaborate with team and cross-functional partners to help guide the Quality Control team to prioritize as the company would
  • Evaluate data, assess, and develop options
  • Comprehensive understanding of all applicable MSOP’s, QCSOP’s, GMP (Good Manufacturing Practices), and line clearance requirements
  • Audit employees and processes to ensure team members, product, and process meet specifications and standards
  • Provide Quality Control with timely performance feedback
  • Maintain J.I.T. (Just In Time) and F.I.F.O. (First In First Out) methodology to optimize production operations
  • Analyze situations and utilize critical thinking skills to prevent or find resolution for production issues
  • Ensure the team, production department and processes are in line with company practices and safety standards
  • Communicate with the production supervisor and other production leads to coordinate production activities and share results
  • Works with cross-functional departments (planning, quality, engineering) to prevent or resolve production issues
  • Initiate and assist with processing Non-Conformance reports and investigation reports
  • Ensure working areas meet the 5’S (sort, set in order, shine, standardize, and sustain) methodology
  • Able to use a microscope and understand magnification levels for visual inspection
  • Perform any other duties as assigned
  • Manage team to ensure that all finished products meet quality standards and specifications
  • Maintain a production environment that complies and follows all quality standards and government regulated standards
  • Performs in-process inspection according to QC WI’s

Requirements

  • High School diploma or equivalent
  • 5+ years of manufacturing experience in the medical device or similar industry
  • Experience with LEAN manufacturing principles
  • Prioritize experience with Coordinate Measuring Machines

Qualifications

  • Proficient computer knowledge of Microsoft Office programs: Outlook, Excel, Word
  • Ability to effectively communicate with others within and outside the organization (i.e. management, supervisors, coworkers, inspectors and auditors from various governing bodies, such as FDA auditors)

Skills

  • Quality control
  • Manufacturing experience
  • LEAN manufacturing principles
  • Coordinate Measuring Machines
  • Microsoft Office proficiency
  • Effective communication

Benefits

  • Medical
  • Vision
  • Dental
  • 401k Matching
  • Employee Assistance Programs
  • Vacation and sick pay

Pay

TBD

Schedule

TBD

Benefits

  • Medical
  • Vision
  • Dental
  • 401k Matching
  • Employee Assistance Programs
  • Vacation and sick pay

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