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Job Title: Quality Assurance InspectorJob Description

Quality Assurance Inspectors play a crucial role in ensuring that manufacturing operations meet the highest standards during the production process. They are responsible for approving raw material documentation associated with incoming plasma shipments from donor collection centers, as well as overseeing in-process production batches at the Plasma Logistics Center (PLC). Inspectors identify and document deviations in materials and the manufacturing process, ensuring these are corrected to deliver a superior finished product for customers.

Responsibilities

+ 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 related to plasma shipments, Production Units (PUs), or final plasma lots.

+ Approve Production Units by verifying customer and regulatory specifications, and communicate required adjustments to the QA Supervisor.

+ Inspect final outgoing plasma lot shipments to ensure all pallets are properly packaged and loaded for sales and distribution.

+ Investigate and report in-process and final product deviations that do not meet quality specifications, documenting these in a deviation report.

+ Participate in the writing or revision of 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.

Essential Skills

+ Good communication skills with the ability to express ideas clearly and thoroughly in both verbal and written communications.

+ Proactive and results-oriented with 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 environment and follow safety guidelines.

+ Computer literacy with experience in Microsoft applications.

+ Ability to perform basic arithmetic functions, including addition, subtraction, multiplication, division, and using decimals.

Additional Skills & Qualifications

+ High School diploma or GED required.

+ 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 is helpful.

+ 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.

Work Environment

This role involves working closely with manufacturing operations during the production process. The position requires adherence to safety guidelines and involves working in a team-oriented environment.

Job Type & Location

This is a Contract position based out of Clayton, North Carolina.

Pay and Benefits

The pay range for this position is $25.22 - $25.22/hr.

Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:

• Medical, dental & vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life & AD&D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave)

Workplace Type

This is a fully onsite position in Clayton,NC.

Application Deadline

This position is anticipated to close on Oct 17, 2025.

About Actalent

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.

The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email [email protected] (%[email protected]) for other accommodation options.