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Quality Control Analyst - Chemistry​/Raw Materials Testing

Job in Erie, Erie County, Pennsylvania, 16501, USA
Listing for: Bayer AG
Full Time position
Listed on 2026-02-12
Job specializations:
  • Quality Assurance - QA/QC
    Quality Technician/ Inspector, Quality Control / Manager, Data Analyst, QA Specialist / Manager
Salary/Wage Range or Industry Benchmark: 60000 - 80000 USD Yearly USD 60000.00 80000.00 YEAR
Job Description & How to Apply Below
Quality Control Analyst - Chemistry/Raw Materials Testing (Contract)

Myerstown, PA, United States (On-site)

Contract (5 months 28 days)

Published a week ago

On hold

Job Title: Quality Control Analyst - Chemistry/Raw Materials Testing

Department/Team

Description:

This position is within the Quality Assurance department. The incumbent will be expected to learn Quality Assurance systems, manufacturing processes, and collaborate effectively with peers in laboratories, Manufacturing/Production, and other departments. The role involves performing quality assurance tests on specific products, impacting material rejection and manufacturing procedures. The Drug Product testing team oversees QC testing of OTC pharmaceuticals, ensuring products meet stability and shelf-life specifications.

The team is fast-paced, aiming to meet throughput times supporting lean manufacturing, with a focus on Finished Goods testing.

Position Summary:

Perform analysis on intermediates and finished products to support product disposition. Assist in troubleshooting and problem-solving as needed.

Position

Duties and Responsibilities:

  • Perform qualitative and quantitative analysis on in-process and finished pharmaceutical products using gravimetric, spectrophotometric, HPLC, and other instrumentation, following approved procedures.
  • Maintain detailed records of all analysis data and ensure proper documentation.
  • Evaluate analysis data, investigate discrepancies, consult with supervisors, and recommend additional testing if necessary.
  • Conduct routine testing to ensure materials meet company and compendia standards.
  • Adhere to safety programs, GMPs, ISO standards, and other regulations.
  • Assist in non-compliance investigations and troubleshooting of analytical methods and instruments.
  • Perform any special assignments as directed by the supervisor.
  • Requirements/Preferences:

    • Bachelor's Degree required.
    • At least 1 year of laboratory experience, preferably in the pharmaceutical industry.
    • Knowledge of statistics, data processing, and GMPs.
    • Understanding of analytical chemistry and experience with laboratory instrumentation such as HPLC, UV, GC, IR, AA.
    • Effective communication skills and ability to work independently and in teams.
    • Strong organizational and planning skills.

    Preferred: Knowledge of NF, USP, EP testing procedures and US pharmaceutical industry standards.

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