Merck KGaA Darmstadt Germany-posted 2 months ago
$65,000 - $75,000/Yr
Full-time • Entry Level
Farmingdale, NJ
Chemical Manufacturing

The position involves working closely with quality engineers to support day-to-day operations, including handling Non Conformance Reports (NCRs), Out of Tolerance Gage Reports, Customer Complaints, and the development and implementation of Corrective and Preventive Actions (CAPA). The role also includes revising Operational Procedures and participating in Continuous Improvement (CI) initiatives. The individual will actively support and participate in special projects and must perform all duties in strict observance of the company's procedures, Good Manufacturing Practices (GMPs), Standard Operating Procedures (SOPs), and other internal and external regulations.

  • Identify, report, and seek corrections for calibration out of tolerance (OOT) incidents in a timely manner.
  • Participate in investigations related to Non Conformance Reports (NCR), Out of Tolerance, and Customer Complaints.
  • Publish Metric Trending Plans for Calibration.
  • Assist with Corrective and Preventive Action (CAPA) resolution.
  • Revise Operational Procedures and support Continuous Improvement (CI) initiatives.
  • Deliver training to team members performing related tasks.
  • Participate in department and cross-functional meetings in the absence of the QA Calibration Engineer.
  • Execute validation protocols, gage repeatability and reproducibility (R&R) testing, and data analysis, completing required reports.
  • Complete Vertex, CMM programming, and SPC template completion.
  • High school diploma or GED is required.
  • 3 years of relevant experience preferred.
  • Proficient technical writing abilities.
  • Broad knowledge of good documentation practices and good manufacturing processes.
  • Ability to read and interpret blueprints and drawings.
  • Knowledgeable in Geometric Dimensioning & Tolerancing (GD&T).
  • Excellent communication, organization, and problem-solving skills.
  • Ability to work with minimum supervision and under pressure.
  • Computer literate in Microsoft Word, Excel, and PowerPoint.
  • Knowledge of FDA & ISO regulations is a plus.
  • ASQ Quality Technician Certification is highly desirable.
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