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Scientist II (ARD)
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Full-time
- Cambrex is a leading global contract development and manufacturing organization (CDMO) that provides drug substance, drug product, and analytical services across the entire drug lifecycle.
- With more than 40 years of experience and a growing team of over 2,000 professionals servicing global clients, Cambrex is a trusted partner in branded and generic markets for API and dosage form development and manufacturing.
- ResponsibilitiesExecute analytical methods for in-process control, release testing and stability monitoring of bulk drug substances and drug products under cGMP guidelinesParticipates in experimental design, including development of methods and testing requirements to demonstrate method suitability.
- Maintains compliant records with little or no supervisionAble to write technical documents with assistanceStrong understanding and proficiency in use and maintenance of instrumentation, equipment, and scientific methodologies necessary to perform assigned tasks Perform assigned tasks carefully, safely and on schedule according to SOPs and supervisor instructionsSets up various instrumentation for testing according to written test methods and with little to no supervision.
- As needed, troubleshoots laboratory instrumentationLeads a sample project with assistanceMay participate in client level meetings, with approvalResponsible for ensuring compliance with cGMP and other regulatory guidelines.
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