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RESPONSIBILITIES:
• Conduct routine and non-routine analysis of raw and starting material samples
• Review analytical data for compliance to SOPs
• Assemble and document data for quality review
• Present and participate in internal and external scientific meetings
• Revise SOPs as needed, e.g., analytical methods, equipment procedures, and material specifications
• Applies knowledge of cGMP and GLP
REQUIREMENTS:
•BS degree in Biology, Chemistry, or a related field
•2+ years of experience in an analytical development or quality control role
•Practical knowledge of HPLC, MS, and GC, including the operation of instrumentation
•Familiarity with GMP requirements, with hands-on GMP experience preferred
•Experience following SOPs and recording data in laboratory notebooks or data collection forms
Reach out to learn more:
alanah@peoplewithchemistry.com
858-429-6147