Quality Assurance Inspector – 1st Shift

Grifols

Quality Assurance Inspector approving plasma materials, production units, and shipments for Grifols’ global healthcare manufacturing operations. Documenting deviations and ensuring regulatory and customer specifications are met.

Posted 8/11/2026full-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 adherence to cGMP guidelines.

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 AssuranceDocumentationInspectionDeviation ReportingBasic Arithmetic

Soft Skills

Verbal CommunicationWritten CommunicationInterpersonal Skills

Tools & Technologies

Microsoft Applications

Certifications & Qualifications

High School DiplomaGED

Industry Keywords

Pharmaceutical IndustryPlasma/Blood BankingMedical Device IndustrySource PlasmaQuality Systems

About the role

Key responsibilities & impact

Approve incoming plasma shipment documentation and raw materials by confirming specifications and reject or return unacceptable materials as directed by the QA Supervisor
Generate and document non-conformance of plasma units or procedures associated with plasma shipments, Production Units, or final plasma lots
Approve Production Units by confirming customer and regulatory specifications and communicate required adjustments to the QA Supervisor
Inspect final outgoing plasma lot shipments to ensure pallets are properly packaged and loaded for sales and distribution
Investigate and report in-process or final products and processes that do not meet quality specifications, documenting deviation reports
Participate in writing or revising policies and standard operating procedures related to Source Plasma and quality systems at GPLC
Execute repetitive functions with strict adherence to procedures and maintain 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 is 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 addition, subtraction, multiplication, division, and using decimals
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

Up to 5% of the company bonus pool
Medical
Dental
Vision
PTO
Up to 5% 401(K) match
Tuition reimbursement
Opportunities for professional growth and career progression