Quality Assurance Inspector (1st Shift)

Jobtailor; Clayton (NC); On-site; USD 42,000 - 62,000; Full time

Job summary

GPLC is seeking a Quality Assurance professional to approve incoming plasma shipment documentation and production units, ensuring compliance with customer and regulatory specifications. You will document non-conformances and deviations, and communicate adjustments to QA supervision.

In this role you will inspect final plasma lot shipments, follow cGMP guidelines, contribute to SOP updates, and maintain meticulous records in the company system.

Qualifications

• High School diploma or GED required.
• Minimum 1 year of Quality Assurance experience.
• 2 years working in pharmaceuticals preferred.
• Experience in pharmaceutical, plasma/blood banking, or medical device industries is ideal.
• Working knowledge of cGMP is helpful.
• Strong verbal and written communication skills.
• Attention to detail and teamwork are essential.

Responsibilities

• Approve incoming plasma shipment documentation by confirming specifications and reject or return unacceptable materials.
• Generate and document non-conformance of plasma units or procedures associated with shipments or final plasma lots.
• Approve Production Units by confirming customer and regulatory specifications and communicate adjustments to 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 SOPs 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.

Skills

Quality Assurance

Documentation

Inspection

Deviation Reporting

Basic Arithmetic

Education

High School Diploma

GED

Tools

Microsoft Applications

Job description

• 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

• 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

Core Competencies

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 Experience


• CGMP Knowledge


• Documentation Skills


• Attention to Detail


• Team Collaboration

ATS Optimization Keywords

Hard Skills

• Quality Assurance


• Documentation


• Inspection


• Deviation Reporting


• Basic Arithmetic

Soft Skills

• Verbal Communication


• Written Communication


• Interpersonal Skills

Certifications & Qualifications

• High School Diploma


• GED

Industry Keywords

• Pharmaceutical Industry


• Plasma/Blood Banking


• Medical Device Industry


• Source Plasma


• Quality Systems

Tools & Technologies

• Microsoft Applications