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Grifols

Quality Assurance Inspector – 2nd Shift

Grifols

. Approve incoming plasma shipment documentation and raw materials against specifications .

Posted 11/11/2026full-timeClayton • North Carolina • United StatesJuniorWebsite

Core Competencies

Role fit
Core Competencies

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Demonstrates expertise in Quality Assurance processes within the pharmaceutical and plasma industries, ensuring compliance with regulatory specifications and maintaining high standards of quality control. Proficient in documentation, inspection, and communication to support operational excellence.

Highest-signal resume keywords
Quality Assurance ExperienceCGMP KnowledgeDocumentation SkillsAttention to DetailTeam Collaboration

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills
Quality AssuranceDocumentationDeviation ReportingInspectionBasic Arithmetic
Soft Skills
Verbal CommunicationWritten CommunicationInterpersonal Skills
Tools & Technologies
Microsoft ApplicationsComputer Literacy
Certifications & Qualifications
High School DiplomaGED
Industry Keywords
PharmaceuticalsPlasmaBlood BankingMedical DeviceCGMP

About the role

Key responsibilities & impact
  • Approve incoming plasma shipment documentation and raw materials against specifications
  • Reject and return unacceptable materials as directed by the QA Supervisor
  • Generate and document non-conformances involving plasma units, procedures, production units, or final plasma lots
  • Approve production units by confirming customer and regulatory specifications
  • Communicate required production adjustments to the QA Supervisor
  • Inspect final outgoing plasma lot shipments to verify pallets are properly packaged and loaded
  • Investigate and report products or processes that do not meet quality specifications
  • Document deviations in deviation reports
  • Participate in writing or revising policies and standard operating procedures for Source Plasma and quality systems
  • Perform repetitive functions while following procedures and maintaining record accountability
  • Document approval activities in the organization's computer system

Requirements

What you’ll need
  • High School diploma or GED
  • Minimum of 1 year of Quality Assurance related experience
  • 2 years working in pharmaceuticals
  • Experience in the pharmaceutical, plasma/blood banking or medical device industry is ideal
  • Working knowledge of cGMP helpful
  • Good verbal and written communication skills
  • Strong attention to detail
  • Strong interpersonal skills
  • Ability to work in a team-oriented environment and follow safety guidelines
  • Computer literacy and experience using Microsoft applications
  • Ability to perform basic arithmetic, including decimals
  • Must work 2nd shift, Monday–Thursday, 1:30pm–12:00am
  • Depending on the area of assignment, directly related experience or a combination of directly related education and experience and/or competencies may be considered in place of the stated requirements

Benefits

Comp & perks
  • Eligible to participate in up to 5% of the company bonus pool
  • Medical insurance
  • Dental insurance
  • Vision insurance
  • Paid time off (PTO)
  • Up to 5% 401(k) match
  • Tuition reimbursement
  • Opportunities for professional growth and career progression