QA Specialist

Momentum Staffing Group LLC

Oak Brook (IL)

On-site

USD 65,000 - 85,000

Full time

2 days ago
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Job summary

Momentum Staffing Group LLC is seeking candidates to join a leading pharmaceutical company's Quality Assurance team in Oak Brook, Illinois. The QA role supports pharmaceutical production by providing quality oversight across multiple production teams and contributing to a dynamic, growth‑oriented environment.

Key responsibilities include investigating deviations (EMCARs), ensuring completeness and accuracy of investigations, assisting other departments as needed, and ensuring compliance with

Qualifications

  • Bachelor's in Science (Biology, Biochemistry, Chemistry, Engineer, Physics) or equivalent.
  • 1-3 years working in a cGMP regulated environment, preferably pharmaceuticals.
  • Knowledge of cGMPs and FDA guidelines.
  • Experience with internal and external audits preferred.

Responsibilities

  • Investigating deviations, including EMCARs, relevant to area of responsibility.
  • Ensuring the completion and accuracy of investigations.
  • Assisting other departments as needed.
  • Ensuring compliance to cGMPs.

Education

Bachelor's in Science (Biology, Biochemistry, Chemistry, Engineer, Physics)

Job description

A leading pharmaceutical company is looking to add members to their growing Quality Assurance team. This position offers exceptional growth opportunities within the industry,a dynamic and challenging work environment, and competitive compensation. QA candidates will support pharmaceutical production by providing quality support and oversight for various production teams.

Qualifications:
  • Investigating deviations, including EMCARs, relevant to area of responsibility.
  • Ensuring the completion and accuracy of investigations.
  • Assisting other departments as needed.
  • Ensuringcompliance to cGMPs.
Requirements:
  • Bachelors in Science(Biology, Biochemistry, Chemistry, Engineer, Physics).
  • 1-3years working in cGMP regulated environment, preferably pharmaceuticals.
  • Knowledge of cGMPs and FDA guidelines.
  • Experience with internal and external auditpreferred.
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