Compensation: $27-$33/hr 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 and/or other paid time off as provided by applicable law.
Shift: 3/12h shifts - 6PM-6AM; rotates week over week!
OT Available
10 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:
Day-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, and/or general chemical testing of raw material/utility, 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 standardization/calibration
-Complete Document Revisions
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