Polysciences technical operations and scientific laboratories offer custom synthesis, contract manufacturing and packaging, and laboratory products. We are proud to offer a broad range of products and tailored solutions for the life sciences, bioprocessing, microparticles, medical device, specialty chemical and eChem industries. We adhere to ISO13485: 2016, FDA cGMP 21 CFR 820 regulations, and SOCMA’s ChemStewards® Management System. We believe the best scientific innovations are built through collaborations.

The QC Analyst I is responsible for performing incoming raw materials, in-process samples, intermediate products, and final products analytical analysis per approved internal and customer specifications following associated procedures to support both product manufacturing and commercial product release. Will work under the supervision of more experienced analysts and follow established procedures and protocols.

Essential Functions:

• Performs routine analytical analysis using the following equipment: volumetric glassware, balances, pH Meter, Conductometer, Karl Fisher (KF), TOC, Turbidimeter, GC (FID/MS), Atomic Absorption (AA), and others as required.

• Responsible for QC data analysis and data entry, using both electronic systems and hard copy documentation following GDP.

• Ability to effectively communicate with cross-functional teams, including production, quality assurance, and planning.
• Reports OOS results to QC Manager or designee and assists with compiling required information to complete the investigation report.

• Performs daily and monthly analytical equipment verification and maintenance.

• Flexibility to handle unexpected situations and make adjustments to ensure compliance with 820 GMP and ISO 13485 standards.

• Assists on the review and revision of procedures and test methods.

• Assists on laboratory inventory maintenance.

• Maintains a safe, clean, and organized environment (5S) for all QC areas.

• Supports process improvements within the QC laboratory.

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.
• 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.

• Experience with Open Lab, Chem Station and/or Empower analytical software preferred.
• Proficiency with Adobe, Microsoft Word and Excel required.