Quality Assurance Specialist

First Priority • Elgin, IL

1d • Onsite

About The Position

First Priority, Inc., an animal health industry manufacturer and supplier of generic pharmaceutical products in Elgin, Illinois, is seeking a dedicated, detail-oriented Quality Assurance Specialist. The role supports efficient production and customer expectations by following cGMP guidelines to inspect production lines, packaging components, and labels, and to release finished products and raw materials. The position is non-exempt and pays $19.00 to $24.00 per hour.

The schedule is either Monday through Thursday, 6:00 AM to 4:30 PM, or Monday through Friday, 7:00 AM to 3:30 PM. The work takes place in a temperature-controlled warehouse/manufacturing environment with low to medium noise. Employees may occasionally encounter odors, noise, dust, and chemicals. The role requires standing for long periods (75%–100%) and consistently lifting boxes and containers weighing up to 20 pounds. On-the-job training is provided in hazardous-material awareness, quality-system procedures and documentation, in-house label software, cGMP, and relevant departmental SOPs. Duties and responsibilities may change at any time.

Requirements

• High school diploma or equivalent.
• Ability to communicate effectively.
• Understanding of weights and measures.
• Ability to work independently and as part of a team, including without direction.
• Ability to stand for long periods (75%–100%).
• Ability to consistently lift boxes and containers weighing up to 20 pounds.

Nice To Haves

• 0–3 years of Quality Assurance experience, preferably in a manufacturing environment.

Responsibilities

• Inspect finished product, brite stock, labels, compounding and production in-process paperwork, packaging, and in-process products for conformance to cGMP standards.
• Issue and reconcile labels, printed packaging, and other controlled secondary packaging, labeling, or documentation as required.
• Use inspection tools and equipment to inspect and release components and materials.
• Document inspection findings on records for production batch records, receiving paperwork, validation protocols, or other required cGMP documentation.
• Work in accordance with company policies and procedures.
• Follow health and safety guidelines, including PPE requirements and safety regulations.
• Perform other duties and special assignments as assigned.

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level
• Education Level: High school or GED