Quality Control Analyst - 3rd Shift

Compensation: $27-$33hr Exact compensation may vary based on several factors, including skills, experience, and education.Benefit packages for this role will start on the 1st day of employment and include medical, dental, and vision insurance, as well as HSA, FSA, and DCFSA account options, and 401k retirement account access with employer matching. Employees in this role are also entitled to paid sick leave andor other paid time off as provided by applicable law.Shift: 312h shifts - 6PM-6AM; rotates week over week!OT Available10 PTO days, 6 sick days per 12 months, renewed upon extension.*Please note - sick days and PTO days cannot be used interchangeably, and do not carry over upon extension.Requirements: A minimum of a bachelors degree in chemistry, or a Scientific related field Minimum 1 year of working in current Good Manufacturing Practices (cGMP) related to the QC laboratory and ability to identify gaps in processes or systems Experience with HPLC, pH testing, Osmo testing, conductivity, or protein concentration Strong pipetting techniquesKnowledge and awareness of compendial (USP, EP, JP, etc.) requirements and standards for QC testing Ability to read and interpret documents such as SOPs, work instructions, test methods and protocolsDay-to-Day: The QC Analyst In-Process Laboratory position supports the Quality Control In-Process and conducts biochemical, microbiological, and general chemical testing of in-process or final product samples submitted to the QC laboratories. The position requires analytical testing to be completed in compliance with all applicable procedures, standards and GMP regulations. This position requires high attention to detail, organizational leadership, interpersonal skills, a quality mindset, critical thinking, and technical writing skills. This position will be the shift leader and primarily work independently.Key Responsibilities:-Perform analytical testing in compliance with applicable GMP regulations while maintaining a safe work environment in compliance with all applicable environmental, health, and safety regulations.-Conduct biochemical, microbiological, andor general chemical testing of raw materialutility, in-process, or final product samples submitted to the QC laboratories.-Perform peer review of laboratory data-Utilize electronic systems i.e. LIMS, MES, LES, Empower, Trackwise, etc. for execution and documentation of testing-Maintain Laboratory Housekeeping including: sample management, reagent prep, instrument standardizationcalibration-Complete Document Revisions

Created: 2025-02-21