Quality Control Chemist - Pharmaceutical Testing Jobs in USA, PA, Myerstwn | Rose International Job

REQUIRED EDUCATION

• Bachelor's degree in Chemistry, Biology, Pharmaceutical Sciences, or related scientific discipline

REQUIRED QUALIFICATIONS

• Minimum 1 year of laboratory experience outside of academic coursework in the pharmaceutical industry
• Knowledge of analytical chemistry principles and laboratory testing methods
• Experience working with analytical instrumentation
• Strong organizational, documentation, and communication skills
• Ability to work independently and collaboratively within a team environment
• Strong analytical problem-solving abilities and attention to detail

PREFERRED QUALIFICATIONS

• Familiarity with GMP-regulated environments
• Experience with HPLC, UV, GC, IR, AA, or wet chemistry methods
• Understanding of USP, NF, and EP testing procedures
• Experience supporting stability programs or finished goods testingSUMMARY

Seeking a motivated and detail-oriented Quality Control Chemist to support analytical testing operations within the Quality Assurance department at its Myerstown, PA pharmaceutical manufacturing facility. This role focuses on testing in-process materials, finished pharmaceutical products, and stability samples to ensure compliance with company and regulatory standards.

This is an excellent opportunity for candidates with laboratory and analytical chemistry experience who are interested in working in a fast-paced GMP-regulated manufacturing environment supporting OTC pharmaceutical products.

RESPONSIBILITIES

• Perform qualitative and quantitative analysis of in-process materials, intermediates, bulk products, and finished pharmaceutical products
• Conduct testing in accordance with company procedures, USP, and NF testing standards
• Utilize analytical instrumentation including HPLC, UV, GC, IR, spectrophotometers, viscometers, and other laboratory equipment
• Perform routine testing of stability program samples and finished goods
• Accurately document laboratory data and maintain permanent testing records
• Evaluate analytical data and assist with investigations involving discrepancies or deviations
• Support troubleshooting of analytical methods and laboratory instrumentation
• Assist with non-compliance investigations and corrective actions
• Ensure compliance with GMP, ISO, safety, and quality regulations
• Collaborate with Quality Assurance, Manufacturing, and Production teams to support operational goals
• Complete additional laboratory assignments as needed
• Drug screen & criminal background check will be required
• Only those lawfully authorized to work in the designated country associated with the position will be considered.
• Please note that all Position start dates and duration are estimates and may be reduced or lengthened based upon a client's business needs and requirements.

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