Quality Control Analyst I

Polysciences, Inc; Warrington Township (Bucks County); On-site; USD 42,000 - 56,000; Full time

Job summary

Polysciences, Inc. in Warrington, PA is hiring a Quality Control Analyst I to help ensure the quality and reliability of our specialty chemical products.

You will perform routine analytical testing and operate a range of laboratory instruments in a collaborative, regulated environment. You will gain hands-on experience with GDP/data integrity, support investigations, and assist with product release alongside Production and QA teams.

Qualifications

• Bachelor's degree in Chemistry or related science field.
• Experience with GDP and data integrity.
• Ability to work in ISO 13485 or FDA GMP environment preferred.
• Strong documentation and software skills.

Responsibilities

• Perform routine analytical testing of raw materials, in-process samples, and finished products.
• Operate instruments including pH meters, GC-FID/MS, TOC analyzers, Karl Fischer titrator, and AA.
• Document results per GDP and ensure data integrity.
• Support investigations of OOS results and assist with documentation.
• Collaborate with QA, Production and Planning to support release.
• Maintain 5S and a clean, safe lab; participate in continuous improvement.

Skills

Analytical Chemistry

Data Analysis

GDP/GMP Documentation

Laboratory Equipment

Education

Bachelor's degree in Chemistry

Tools

OpenLab

ChemStation

Empower

Job description

Quality Control Analyst ILocation: Warrington, PACompany: Polysciences, Inc.Join Our Team at Polysciences!Are you passionate about analytical chemistry and looking to grow your career in Quality Control? Polysciences, Inc. is seeking a detail-oriented and motivated Quality Control Analyst I to join our Quality Control team in Warrington, PA.In this hands-on laboratory role, you will play an important part in ensuring the quality, consistency, and reliability of our specialty chemical products. Working alongside experienced analysts, you will gain valuable experience with analytical instrumentation, quality systems, and regulated manufacturing processes while supporting production and commercial product release.This is an excellent opportunity for an early-career scientist who enjoys laboratory work, problem-solving, and contributing to a collaborative team environment.What You'll DoPerform routine analytical testing of incoming raw materials, in-process samples, intermediate products, and finished products in accordance with approved specifications and procedures.Operate a variety of analytical laboratory instruments, including pH meters, conductivity meters, Karl Fischer titrators, Total Organic Carbon (TOC) analyzers, turbidimeters, Gas Chromatography (GC-FID/MS), Atomic Absorption (AA) instruments, balances, and volumetric glassware.Analyze, document, and maintain accurate laboratory testing results in accordance with Good Documentation Practices (GDP) and data integrity requirements.Support investigations of Out-of-Specification (OOS) results by promptly reporting findings and assisting with documentation and data collection.Perform routine instrument verification, calibration checks, and preventive maintenance to ensure equipment reliability.Collaborate with Production, Quality Assurance, and Planning teams to support manufacturing schedules and timely product release.Assist with the review and revision of laboratory procedures, analytical methods, and testing documentation.Support laboratory inventory management and ensure adequate availability of testing supplies.Maintain a clean, safe, and organized laboratory environment following 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.What We're Looking ForRequired Qualifications:Bachelor's degree in Chemistry or a related scientific discipline.Knowledge of analytical laboratory techniques, instrumentation, and data analysis.Strong attention to detail with a commitment to accuracy, quality, and documentation.Proficiency in 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.Preferred Qualifications:At least one year of laboratory experience in an ISO 13485 or FDA GMP-regulated environment.Experience with GMP documentation practices, laboratory data integrity, and quality control testing.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 instrumentation such as GC, Karl Fischer titration, TOC, or Atomic Absorption.Why Join Polysciences?At Polysciences, you'll have the opportunity to build your technical expertise while contributing to the quality of products used across a variety of scientific and industrial applications. We value collaboration, continuous improvement, and a commitment to excellence.As a member of our Quality Control team, you'll work in a dynamic laboratory environment where your contributions directly support product quality, manufacturing operations, and customer satisfaction.Ready to take the next step in your chemistry career?Apply today and explore the opportunities waiting for you at Polysciences, Inc.!QualificationsEducation Required: Bachelor's Degree Preferred: Bachelor's DegreeCertification(s): Specify preferred or required.Computer Skills Required: Specify preferred or required.Experience with Open Lab, Chem Station and/or Empower analytical software preferred.Proficiency with Adobe, Microsoft Word and Excel required.Other qualifications:Bachelor’s degree in chemistry or related science field required.At least one (1) year of experience working in an ISO 13485 or FDA GMP regulated environment preferred.Bachelor’s degree in chemistry or related science field required. At least one (1) year of experience working in an ISO 13485 or FDA GMP regulated environment preferred.Experience with quality control GMP documentation of analytical testing results and assurance of laboratory data integrity and compliance preferred.Knowledge of analytical equipment, analytical methods, and data analysis required.Knowledge of compendial methods (ie. USP, EP, ISO, ASTM) preferred.Immediate Work Environment:X-Chemicals Unprotected Height X-Fumes/Gases Persistent NoiseX-PPE used: Lab Coat, Safety Shoes, and Safety GlassesWork Activity: [must equal number of hours worked per day]Stand: 4 Frequency: Intermittently Walk: 1 Frequency: IntermittentlySit: 3 Frequency: Intermittently Drive: 0 Frequency: Choose an item.Lift/Carry DemandsFrequency: Lift/Carry Equipment Provided:0-10 lbs. 1-3 hours a day Reagents Bottles Carriers11-25 lbs. Not Daily Rolling Cart26-50 lbs. Rarely Gas Tank Hand Cart/Drum Lift Cart51-75 lbs. Never Click or tap here to enter text.76-100 lbs. 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