Quality Specialist

Quality Specialist

SRG offers flexible staffing solutions with a national presence. We provide contract, contract-to-hire, direct hire and executive search services. SRG utilizes an innovative approach to identify and qualify talent that is unique to the Staffing industry, featuring a cutting-edge platform that allows us to rapidly and precisely match professionals to client requirements. We have a proprietary database of over one million candidates and maintain continuous contact with our qualified talent.

• Title: Quality Specialist
• Location: South Chipeta Way, UT
• Industry: Pharmaceutical
• Hours: Monday - Friday 9:00 am to 5:00 pm (min of 20 hours a week plus.)
• Salary: $23/HR
• Employment Type: Contract with the potential for direct hire

Essential Areas of Responsibility

• Creation of all the raw material folders Test Request, Status Sheet, Sampling Sheet
• Daily check of items awaiting approval for MS
• Verify all test attribute specifications on the certificate of analysis match the MS
• Ensure all test results from the manufacturer/vendor are within our specification range
• Ensure the manufacturer location matches on the certificate of analysis and packing list to our MS.
• Reach out to PPIC to request a new certificate of analysis or packing list if any discrepancies
• Reach out to QC and QA to make sure that vendor is on approved list, or request DC-057
• Assist in sampling incoming raw material / full room cleans
• Verify system status in SAP for every raw material folder
• Reach out to appropriate department if an inspection lot is in CRTD Status
• Verify there is a LIMS sample number, and reach out to appropriate department if there is none
• Follow up with all appropriate departments to ensure all required information and paperwork is needed to begin sampling incoming material
• Create raw material folder for non-MS items and deliver to QA to be released
• Order and restock sampling items / tools
• Review and request new Sample/Room Logbooks from Doc Control
• Complete and submit Document Submission Form DC-115 to Doc Control.

Position Requirements

• Requires High School Diploma or equivalent.
• Prefer previous experience in a manufacturing environment within pharmaceutical, nutraceutical or food processing industries.
• Attention to detail
• Good with computers
• Quality Specialist experience recommended but not required

EOE/ADA

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