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Grifols

Product Inspector – 2nd Shift

Grifols

Product Inspector ensuring plasma units meet safety standards in a manufacturing environment. Performing inspections, scanning, and record-keeping for quality assurance processes.

Posted 7/2/2026full-timeClayton • North Carolina • 🇺🇸 United StatesJuniorMid-LevelWebsite

Core Competencies

Role fit
Core Competencies

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Demonstrates expertise in plasma management processes, including scanning, visual inspection, and compliance with cGMPs and industry standards. Proficient in maintaining record accountability and following standard operating procedures with minimal supervision.

Highest-signal resume keywords
Plasma Management System (SGP)CGMP KnowledgeVisual InspectionBarcode ScanningStandard Operating Procedures

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills
Plasma Management System (SGP)Visual InspectionBarcode ScanningRecord AccountabilityBasic Math SkillsBasic Computer Skills
Soft Skills
Verbal CommunicationWritten Communication
Industry Keywords
ManufacturingPharmaceuticalFDA Licensed IndustryCGMPsIndustry Standards

About the role

Key responsibilities & impact
  • Position requires scanning and removal of unsuitable plasma units utilizing the Plasma Management System (SGP).
  • A visual inspection of plasma units is also performed, removing any units which are unacceptable.
  • Employee must be able to perform secondary verifications and perform end of PU line clearances.
  • Scanning of plasma units assigned to a PU utilizing a barcode reader.
  • Scanning of archive samples assigned to a SA utilizing a barcode reader.
  • Transferring units to a Sub-shipment during the PU process.
  • Entering "Statistics" during the PU process.
  • Sub-shipment verification at the end of the PU process.
  • “Blocking” of units which do not meet customer requirements.
  • Responsible for various rejections found during visual inspection.
  • Removal of unsuitable plasma units marked for removal in SGP during the PU process.
  • Able to maintain record accountability.
  • Able to perform job duties with minimum supervision.
  • Ability to follow written procedures.
  • Monitoring plasma time out of freezer.

Requirements

What you’ll need
  • High School diploma or equivalent.
  • Two years' experience in Manufacturing, Pharmaceutical or other FDA licensed Industry is desirable.
  • Knowledge of cGMPs and Industry Standards.
  • Ability to follow "Standard Operating Procedures".
  • Possess good verbal and written communication skills.
  • Possess basic math skills (addition, subtraction, division, multiplication).
  • Basic Computer skills.

Benefits

Comp & perks
  • Personal protective equipment required such as protective eyewear, safety shoes, gloves and garments.
  • Health and safety practices.
  • Work is performed standing and walking for 6-8 hours per day.
  • Frequent moderate lifting and carrying of 15-44lbs.
  • Frequent heavy lifting and carrying of 45lbs. with a maximum lift of 50lbs.