Quality Control Senior Associate

Duration Contract 12 months Mode 100% Onsite - Rhode Island Timings Standard 8-5 local hours Description The role will be on-site based out of Rhode Island and will work under the mentorship of the front-line manager. The Bioanalytics team provides analytical expertise in testing in-process, release, and stability samples. The laboratory employs a variety of test methodologies using sophisticated equipment including HPLC/UPLC, capillary electrophoresis and general chemistry methodologies such as appearance, color, clarity, pH, osmolality, polysorbate, protein concentration, and sub-visible particle testing. Responsibilities Follow safety guidelines, cGMPs (Good Manufacturing Practices) and other applicable regulatory requirements Generate complete, accurate, and concise laboratory documentation using electronic systems and laboratory notebooks Ensure that facilities, equipment, materials, organization, processes, procedures and products follow cGMP practices and other applicable regulations Operate laboratory equipment and instrumentation Perform review and approval of assays, documents and records Support continual improvement initiatives Alert management of quality, compliance, supply and safety risks Participate in laboratory investigations Perform general laboratory housekeeping activitiesComplete required assigned training to permit carry through of required tasks Perform additional duties as specified by management Basic Qualifications Master's Degree OR Bachelor's Degree and 1-2 years of Quality experience OR Associate's degree and 6 years of Quality experience OR High school diploma/GED and 8 years of Quality experience Preferred Qualifications 1-2 years’ experience in HPLC/UPLC, capillary electrophoresis and general chemistry methodologies such as appearance, color, clarity, pH, osmolality, polysorbate, protein concentration, and sub-visible particle testing Demonstrated experience in laboratory investigations, method validation, audits, QC processes Proven ability to interpret scientific data Self-motivated, strong organizational skills and ability to manage multiple tasks at one time with minimal direction Top 3 Must Have Skill Sets HPLC, Quality Control, Laboratory chemistry experience Day To Day Responsibilities Testing and review samples in QC/GMP labs. Support other non-routine activities. Equal Opportunity Employer Statement US Tech Solutions is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, colour, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran. AI Statement By applying, you acknowledge that AI-assisted tools may be used during hiring. #J-18808-Ljbffr