Job Description

Chemist – Great Career Opportunity!

Eastridge Workforce Solutions is seeking a Chemist III for our client in Lynwood, CA. This is an opportunity to work with a pharmaceutical company that offers stability, room for growth and great benefits. 

Location: Lynwood, CA
Salary: $75,000 - $85,000 Annually
Job Type: Full-Time | Monday-Friday

Why Join Us?

• Competitive Pay & Benefits – Health, Holiday/ PTO, 401(k)

• Career Growth – Training & Leadership Development Programs

• Innovative Culture – Work with a dynamic, forward-thinking team

What You’ll Do:

• Chemical Analysis: Perform a wide range of chemical analyses on pharmaceutical compounds, raw materials, and finished products using various techniques such as chromatography, spectroscopy, titration, and wet chemistry methods. Ensure compliance with established protocols, standard operating procedures (SOPs), and regulatory requirements.

• Method Development and Validation: Design, develop, optimize, and validate analytical methods for the analysis of pharmaceutical products. Collaborate with cross-functional teams to establish robust analytical methods that meet regulatory guidelines and industry standards.

• Research and Development: Conduct research to explore new methodologies, technologies, and instruments for improved analysis and characterization of pharmaceutical compounds. Stay up-to-date with the latest advancements in the field and implement relevant techniques to enhance analytical capabilities.

• Documentation and Reporting: Maintain accurate and detailed laboratory records of experimental procedures, observations, and results. Prepare technical reports summarizing findings, data analysis, and conclusions. Ensure documentation complies with internal quality management systems and regulatory guidelines.

• Equipment Operation and Maintenance: Operate and maintain sophisticated laboratory equipment, such as high-performance liquid chromatography (HPLC), gas chromatography (GC), mass spectrometry (MS), and dissolution testers. Troubleshoot equipment issues and perform routine maintenance to ensure reliable and accurate results.

• Quality Control and Compliance: Adhere to Good Laboratory Practices (GLP), Good Manufacturing Practices (GMP), and other regulatory guidelines applicable to the pharmaceutical industry. Assist in internal and external audits, address non-compliance issues, and participate in continuous improvement initiatives.

• Cross-functional Collaboration: Collaborate with scientists, engineers, formulation experts, and other stakeholders to support product development, process optimization, and troubleshooting activities. Provide technical guidance and expertise to junior chemists and laboratory staff.

• Safety and Risk Management: Maintain a safe and clean working environment by following safety protocols, handling hazardous materials appropriately, and practicing good laboratory hygiene. Identify and mitigate potential risks associated with chemical handling, laboratory procedures, and equipment operation.

What We’re Looking For:

• Bachelor's degree in Chemistry, Pharmaceutical Sciences, or a related field. A higher degree or additional certifications may be preferred.

• Extensive experience (5+ years) working in a pharmaceutical research and development laboratory, preferably in an analytical role.

• Strong knowledge of analytical techniques, instrumentation, and methodologies commonly used in pharmaceutical analysis.

• Familiarity with regulatory guidelines and quality management systems (e.g., FDA, ICH, USP, etc.) governing the pharmaceutical industry.

• Proficient in data analysis and interpretation using statistical software or other relevant tools.

Ready to take the next step in your career? Apply Today!

#IPROPLUS

#LI-SM3

Job Tags

Similar Jobs