In-Process QC Analyst conducting laboratory tests for quality control in a leading CDMO specializing in pharmaceuticals. Responsible for analysis and training in laboratory settings.
Responsibilities
Performs laboratory tests to determine chemical and physical characteristics or composition of solid and liquid materials for quality control and process control
Runs standard and advanced analysis in-process, raw material, intermediate and final release samples
Analyzes batches of drug substance and/or intermediates to be used in clinical or registration programs
Handles potent materials per applicable procedures and training
Performs qualitative tests or quantitative assays on samples using standard analytical equipment
Responsible for training new chemists as needed
Ensures laboratory productivity and turnaround goals are met
Requirements
Bachelor's Degree from four-year college or university in Chemistry or related science field
Two years’ experience in a laboratory; or equivalent combination of education and experience
Ability to read, analyze, and interpret common scientific and analytical journals, financial reports, and legal documents
Ability to respond to common inquiries or complaints from customers, regulatory agencies, or members of the business community
Ability to write speeches and articles for publications that conform to prescribed style and format
Ability to effectively present information to top management, public groups, and/or boards of directors
Ability to apply advanced mathematical concepts such as exponents, logarithms, quadratic equations, and permutations
Ability to apply statistical concepts such as significant figures and analysis of variance
Benefits
401(k) matching - Corden Pharma will contribute 100% of the first 6% - 100% vested after 2 years of service
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