Bayer AG
Quality Control Analyst - Chemistry/Raw Materials Testing
Bayer AG, Phila, Pennsylvania, United States
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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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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