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QA Technical Associate

Job in South Beloit, Winnebago County, Illinois, 61080, USA
Listing for: Medix™
Full Time position
Listed on 2026-01-12
Job specializations:
  • Quality Assurance - QA/QC
    Quality Control / Manager, QA Specialist / Manager, Quality Technician/ Inspector, Data Analyst
Job Description & How to Apply Below
Position: QA Technical Associate - 248622

This role supports Quality Assurance activities across analytical, laboratory, and product development functions in a regulated pharmaceutical environment. The position ensures that documentation, data, and processes comply with cGMP and internal quality standards while supporting batch release, stability, and continuous improvement activities.

Required Qualifications
  • Strong knowledge of cGMP and regulatory requirements.
  • Strong organizational, documentation, and time‑management skills.
  • Proficiency in Microsoft Word and Excel.
  • Strong technical writing skills; ability to provide writing samples upon request.
  • Ability to work independently and collaboratively in a cross‑functional team environment.
Key Responsibilities
  • Provide QA support for analytical testing, product development, and formulation activities, including protocol review and approval.
  • Review and approve analytical reports; interpret data to ensure compliance with specifications and regulatory expectations.
  • Support review of CMC sections of regulatory submissions such as abbreviated new drug applications (ANDAs).
  • Manage document activation, control, and distribution for SOPs, specifications, protocols, and related controlled documents.
  • Review, interpret, trend, and approve stability study data.
  • Issue and maintain preventative maintenance and calibration documentation.
  • Support laboratory audits and inspections, including preparation and follow‑up activities.
  • Maintain, issue, and review batch records; perform final batch record review, release, and pedigree issuance.
  • Support and maintain data within specialized quality and laboratory systems, including calibration systems, document management systems, and temperature monitoring systems.
  • Author and support deviation, incident, and investigation documentation.
  • Provide technical and quality support to laboratory, manufacturing, and product development teams as needed.
Seniority Level

Not Applicable

Employment Type

Full-time

Job Function

Quality Assurance

Industries

Staffing and Recruiting and Pharmaceutical Manufacturing

Medical insurance

Vision insurance

401(k)

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Position Requirements
10+ Years work experience
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