Data Reviewer - Quality Control

Quality Control InspectorPay Range: $25 to $28 an hour.Client Industry: PharmaceuticalJob Mode: OnsiteShift: 2nd Shift from Sunday–Thursday, 2:00 PM–10:30 PMDuration: 6 Months Contract – Possible Extension based on performance and business needsJob Summary: The Quality Control Inspector supports data review activities within a fast paced GMP laboratory environment. The role focuses on reviewing laboratory data supporting raw materials, environmental monitoring, in process, final bulk, stability, and validation activities. The position ensures laboratory records and data are accurate, complete, compliant, and properly archived. The ideal candidate has strong organizational and time management skills and can complete assigned responsibilities within established timelines. This role works under supervision while collaborating with laboratory and quality teams to support operational objectives.Key Responsibilities:Perform routine review of laboratory test data including on the floor and off the floor review for low complexity test methods.Archive laboratory data and records within the RIMS system.Review assays, analytical data, laboratory records, calculations, and supporting documentation for accuracy and compliance.Maintain GMP requirements for laboratory records, procedures, systems, and documentation.Support data mining projects and assigned laboratory data review activities.Manage logbooks, scanning, filing, and other administrative documentation activities.Complete assigned tasks within established timelines and communicate progress or issues to appropriate team members.Maintain a safe and compliant laboratory work environment.Participate in training activities by demonstrating procedures and processes to other employees.Required Qualifications:Bachelor's degree in a relevant scientific discipline or High School Diploma with 5 or more years of combined manufacturing, quality assurance, or quality control experience in the pharmaceutical or biologics industry.Experience working in a GMP laboratory environment.Experience with RIMS, Empower, and A280.Ability to work onsite Sunday through Thursday from 2:00 PM to 10:30 PM.Preferred Qualifications:Experience supporting pharmaceutical or biologics manufacturing operations.Experience with environmental monitoring, stability, validation, raw material, in process, or final bulk testing.Experience with laboratory data archiving and data management.Experience with low complexity analytical test methods.Benefits: The Company offers the following benefits for this position, subject to applicable eligibility requirements: medical insurance, dental insurance, vision insurance, 401(k) retirement plan, life insurance, long-term disability insurance, short-term disability insurance, paid parking/public transportation, paid time off, paid sick and safe time, hours of paid vacation time, weeks of paid parental leave, paid holidays annually - AS Applicable