Polymer & Material Testing Scientist

Key Responsibilities

• Perform formulation, polymerization, processing and evaluation of methyl polydimethlysiloxane (mPDMS) used in silicon hydrogel monomers, ensuring batch quality for approved use by raw material suppliers
• Represent the QA Laboratories on cross functional project teams and as ad hoc committees supporting New Product Introductions (NPI), product quality protocols, polymerization issues and other production issues as applicable
• Support non‑routine test requests, material assessments and complaint investigations
• Work closely with Product Quality Management on critical issues related to monomer, polymerization and process issues
• Lead OOS/OOT investigations within the QA Labs and support identified corrective/preventative actions from a laboratory perspective, including initiating, escalating and supporting non‑conformances and quality events
• Proactively identify issues/opportunities in the QA Labs and seek appropriate actions (e.g., procedure/method improvements and instrument upgrades)
• Mentor junior scientists on new laboratory methodologies, instrumentation and techniques, fostering a positive and collaborative team culture
• Understand product portfolio and potential process charges that could affect product quality
• Support test method transfers into the QA Raw Materials and Finished Goods laboratories from R&D

• Bachelor's or Master's degree in Polymer Science, Materials Science, Chemical Engineering, or related scientific field

• Minimum of 4 years of chemistry or related field experience in a Quality Assurance / Quality Control Laboratory environment
• Proven experience in polymer synthesis, formulation and process troubleshooting within a Quality Assurance / Quality Control environment
• Experience with analytical techniques such as GC, HPLC/UPLC, FTIR, UV‑Vis and refractometer
• Ability to interpret complex data and troubleshoot technical issues systematically
• Excellent communication and team collaboration skills
• Attention to detail and strong problem‑solving capabilities
• Knowledge of regulatory standards relevant to medical devices (e.g., FDA, ISO and GLP)
• Familiarity with Lean Principles, Six Sigma, Process Excellence and Project Management
• Strong proficiency in Microsoft Office Suite, including Word, Excel, PowerPoint, and Outlook for laboratory documentation, data analysis, and reporting

• Proficient in Labware Laboratory Information Management System (LIMS) for data entry, sample tracking, and report generation
• Demonstrates strong proficiency in Empower Chromatographic System for data acquisition, analysis, and reporting
• Proficient in SAP system for inventory management, data entry, and process tracking

Specialist Staffing Group is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status.