Quality Control Analyst I

Polysciences, Inc.•Warrington Township, PA
•$59,200 - $69,800•Onsite

About The Position

Polysciences, Inc. is seeking a detail-oriented Quality Control Analyst I for its Quality Control team in Warrington, Pennsylvania. This hands-on laboratory position supports the quality, consistency, and reliability of specialty chemical products through analytical testing, documentation, instrument upkeep, and collaboration with manufacturing and quality teams. The role offers the opportunity to develop expertise with analytical instrumentation, quality systems, and regulated manufacturing processes while supporting production and commercial product release. The analyst performs routine testing on incoming raw materials, in-process samples, intermediates, and finished products according to approved specifications and procedures. The role follows Good Documentation Practices and data-integrity requirements, supports investigations into out-of-specification results, and works in accordance with laboratory procedures and applicable FDA GMP and ISO 13485 requirements. The position is full-time, with a Monday–Friday first shift and no travel.

Requirements

  • Bachelor's degree in Chemistry or a related scientific discipline.
  • Knowledge of analytical laboratory techniques, instrumentation, methods, and data analysis.
  • Strong attention to detail and commitment to accuracy, quality, and documentation.
  • Proficiency with Microsoft Word, Excel, and Adobe applications.
  • Strong organizational, communication, and problem-solving skills.
  • Ability to follow established procedures, manage multiple priorities, and work effectively in a team-oriented laboratory environment.

Nice To Haves

  • At least one year of laboratory experience in an ISO 13485- or FDA GMP-regulated environment.
  • Experience with GMP documentation practices, analytical testing records, laboratory data integrity, and compliance.
  • Familiarity with analytical software such as OpenLab, ChemStation, or Empower.
  • Knowledge of compendial testing methods and standards, including USP, EP, ISO, and ASTM.
  • Experience with analytical instruments such as GC, Karl Fischer titration, TOC, or Atomic Absorption.

Responsibilities

  • Perform routine analytical testing of incoming raw materials, in-process samples, intermediate products, and finished products according to approved specifications and procedures.
  • Operate analytical laboratory instruments, including pH and conductivity meters, Karl Fischer titrators, TOC analyzers, turbidimeters, GC-FID/MS, Atomic Absorption instruments, balances, and volumetric glassware.
  • Analyze, document, and maintain accurate test results in accordance with Good Documentation Practices and data-integrity requirements.
  • Promptly report findings and assist with documentation and data collection for Out-of-Specification investigations.
  • Perform routine instrument verification, calibration checks, and preventive maintenance.
  • Collaborate with Production, Quality Assurance, and Planning teams to support manufacturing schedules and timely product release.
  • Assist with reviewing and revising laboratory procedures, analytical methods, and testing documentation.
  • Support laboratory inventory management and maintain availability of testing supplies.
  • Maintain a clean, safe, and organized laboratory in accordance with 5S principles.
  • Participate in continuous-improvement initiatives to enhance laboratory efficiency, quality, and compliance.
  • Follow established laboratory procedures and quality standards, including applicable FDA GMP and ISO 13485 requirements.
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