What are the responsibilities and job description for the Chemical Methods Specialist position at Consumer Product Partners?
Company Overview: As a leading manufacturer of over-the-counter (OTC) drugs and cosmetics, Consumer Product Partners is committed to delivering high-quality products while prioritizing employee satisfaction. We are seeking a highly skilled Analytical Chemist/Methods Engineer to join our team in the development of robust analytical methods.
Key Responsibilities include designing, developing, validating, and verifying analytical methods for testing raw materials, finished products, stability, and process validation. The successful candidate will conduct analysis of Active Pharmaceutical Ingredients (APIs), excipients, and finished drug products according to company Standard Operating Procedures (SOPs), current Good Manufacturing Practices (cGMPs), Good Laboratory Practices (GLPs), Good Distribution Practices (GDPs), and FDA/DEA/OSHA regulations. Additional responsibilities include developing and executing protocols, reports, and test methods related to raw material and finished product testing, providing technical expertise to support laboratory investigations and method transfers between facilities, operating and troubleshooting routine laboratory equipment, and utilizing Empower software for data analysis and method development.
Required Qualifications and Skills include a Bachelor's degree in analytical chemistry, organic chemistry, biochemistry, or food science with coursework in analytical chemistry. A minimum of 3 years of laboratory experience in method development, validation, verification, and transfer activities for pharmaceutical raw materials and finished products is also required. Proficiency in operating laboratory instrumentation and conducting statistical analysis, as well as strong knowledge of USP, FDA, and ICH guidelines, are essential. Effective communication skills and the ability to work independently with minimal supervision are also necessary. Proven ability to organize projects and complete tasks in a timely manner is a must.
Key Responsibilities include designing, developing, validating, and verifying analytical methods for testing raw materials, finished products, stability, and process validation. The successful candidate will conduct analysis of Active Pharmaceutical Ingredients (APIs), excipients, and finished drug products according to company Standard Operating Procedures (SOPs), current Good Manufacturing Practices (cGMPs), Good Laboratory Practices (GLPs), Good Distribution Practices (GDPs), and FDA/DEA/OSHA regulations. Additional responsibilities include developing and executing protocols, reports, and test methods related to raw material and finished product testing, providing technical expertise to support laboratory investigations and method transfers between facilities, operating and troubleshooting routine laboratory equipment, and utilizing Empower software for data analysis and method development.
Required Qualifications and Skills include a Bachelor's degree in analytical chemistry, organic chemistry, biochemistry, or food science with coursework in analytical chemistry. A minimum of 3 years of laboratory experience in method development, validation, verification, and transfer activities for pharmaceutical raw materials and finished products is also required. Proficiency in operating laboratory instrumentation and conducting statistical analysis, as well as strong knowledge of USP, FDA, and ICH guidelines, are essential. Effective communication skills and the ability to work independently with minimal supervision are also necessary. Proven ability to organize projects and complete tasks in a timely manner is a must.
