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Quality Assurance Inspector
Job Location:
Job Location:
Clayton, OH - USA
Monthly Salary:
Not provided by the employer
Monthly Salary:
Posted:
1 July 2026 (30+ days ago)
Posted:
Application Deadline:
28 September 2026
Application Deadline:
Vacancies:
1 Vacancy
Vacancies:
Job Summary
Job Title: Quality Assurance Inspector
Location: Clayton NC 27520
1st Shift 5:00 AM to 1:30 PM
2nd Shift 1:30 p.m. to 12:00 a.m.
Summary
Quality Assurance Inspectors work with manufacturing operations during the production process approving raw materials and associated documentation for incoming plasma shipments from donor collection centers and the in-process production batches (Production Units - PUs) at the Plasma Logistics Center (PLC). Quality Assurance Inspectors identify and document deviations of both materials and the manufacturing process and ensure these deviations are corrected to ensure a better finished product for prospective customers.
Primary Responsibilities
* Approves incoming plasma shipment documentation and raw materials by confirming specifications rejects and returns unacceptable materials as directed by QA Supervisor.
* Generates and documents non-conformance of plasma units or procedures associated with plasma shipments PUs or final plasma lots.
* Approves PUs by confirming customer and regulatory specifications and communicating required adjustments to the QA Supervisor.
* Responsible for inspecting final outgoing plasma lot shipments to ensure all pallets are properly packaged and loaded for sales and distribution.
* Investigates and reports in-process/final product and processes that do not meet quality specifications and document in a deviation report.
* Participates in the writing or revision of policies and standard operating procedures related to Source Plasma and quality systems at GPLC.
* Executes repetitve functions with strict adherence to procedures and maintains record accountability.
* Documents approval activities in the organizations computer system.
Knowledge Skills and Abilities
* Good communication skills with the ability to express ideas with clarity and thoroughness in both verbal and written communications.
* Proactive results oriented with a strong attention to detail.
* Strong interpersonal skills to interface with manufacturing operators and various levels of management as well as with support and service departments.
* Ability to work in a team-oriented enviroment and follow safety guidelines.
* Must be computer literate with experience in the use of Microsoft applications.
* Able to perform basic arithmetic functions including addition subtraction multiplication division and using decimals.
Education
High School diploma or GED.
Experience
* Typically requires a minimum of **1 year of Quality Assurance related experience** and **2 years working in pharmaceuticals**.
* Experience in the pharmaceutical plasma/blood banking or medical device industry is ideal.
* Working knowledge of **cGMP** helpful.
Quality Assurance Inspectors work with manufacturing operations during the production process approving raw materials and associated documentation for incoming plasma shipments from donor collection centers and the in-process production batches (Production Units - PUs) at the Plasma Logistics Center (PLC). Quality Assurance Inspectors identify and document deviations of both materials and the manufacturing process and ensure these deviations are corrected to ensure a better finished product for prospective customers.
Primary Responsibilities
* Approves incoming plasma shipment documentation and raw materials by confirming specifications rejects and returns unacceptable materials as directed by QA Supervisor.
* Generates and documents non-conformance of plasma units or procedures associated with plasma shipments PUs or final plasma lots.
* Approves PUs by confirming customer and regulatory specifications and communicating required adjustments to the QA Supervisor.
* Responsible for inspecting final outgoing plasma lot shipments to ensure all pallets are properly packaged and loaded for sales and distribution.
* Investigates and reports in-process/final product and processes that do not meet quality specifications and document in a deviation report.
* Participates in the writing or revision of policies and standard operating procedures related to Source Plasma and quality systems at GPLC.
* Executes repetitve functions with strict adherence to procedures and maintains record accountability.
* Documents approval activities in the organizations computer system.
Knowledge Skills and Abilities
* Good communication skills with the ability to express ideas with clarity and thoroughness in both verbal and written communications.
* Proactive results oriented with a strong attention to detail.
* Strong interpersonal skills to interface with manufacturing operators and various levels of management as well as with support and service departments.
* Ability to work in a team-oriented enviroment and follow safety guidelines.
* Must be computer literate with experience in the use of Microsoft applications.
* Able to perform basic arithmetic functions including addition subtraction multiplication division and using decimals.
Education
High School diploma or GED.
Experience
* Typically requires a minimum of **1 year of Quality Assurance related experience** and **2 years working in pharmaceuticals**.
* Experience in the pharmaceutical plasma/blood banking or medical device industry is ideal.
* Working knowledge of **cGMP** helpful.
