Scientist – Analytical Testing Specialist
QvalFocus Inc. · Mansfield, MA · 2 days ago
On-siteAnalystFull-time
Title: Scientist Analytical Testing Specialist Location: Mansfield, MA Fully Onsite Type Of Job: Contract Duration: 6 Months Job Description We are looking for experienced Analytical Testing Scientists to support pharmaceutical Quality Control laboratory operations. The role will focus on routine analytical testing, laboratory investigations, data review, and documentation within a regulated GMP environment. Candidates should have strong hands-on laboratory experience and be comfortable independently performing analytical testing while maintaining data integrity and GMP documentation requirements. Responsibilities Perform routine pharmaceutical QC testing using analytical laboratory instruments and established test methods.Perform hands-on testing using HPLC, GC, dissolution equipment, UV/Vis spectrophotometers, and general wet chemistry techniques.Support raw material, in-process, finished product, release, and stability testing activities.Execute analytical methods according to approved procedures, specifications, and laboratory standards.Review analytical data, chromatograms, calculations, and test results for accuracy and completeness.Support laboratory investigations associated with atypical, OOS, OOT, or questionable results.Maintain complete and accurate laboratory records in accordance with GMP and Good Documentation Practices.Ensure laboratory activities comply with applicable data integrity and quality requirements.Assist with troubleshooting analytical methods and laboratory instrumentation when required.Work closely with QC, QA, and laboratory management to support timely completion of testing activities. Qualifications Minimum 5 7 years of pharmaceutical QC or analytical laboratory experience.Strong hands-on experience with HPLC and other pharmaceutical analytical testing techniques.Experience with GC, dissolution, UV/Vis, and wet chemistry is highly preferred.Experience supporting pharmaceutical product release and stability programs.Good understanding of GMP laboratory practices, data integrity, and laboratory documentation.Ability to work independently in a fast-paced laboratory environment.