Scientist, Analytical R&D; (FullTime)

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Increase in project workload related to Macugen filing, aPDGF project timlines and workload.

Summary

• Conduct experiments and perform analyses independently. Validate analytical methods; perform physicochemical studies under direction of supervisor.
• Analyze assigned samples by following applicable methods.
• Maintain analytical instrumentation and associated doucmentation such as logbooks, etc.
• Attend seminars and training courses relevant to analytical chemistry, the pharmaceutical industry, and the Eyetech franchise.
• Conduct all analyses in a consistent state of cGMP compliance.
• Provide input and data for inclusion into scientific reports and regulatory documentation.
• Keep compliant notebook and/or data sheets summarizing all experiments and/or analyses.

Qualifications

• BA/BS in chemistry, biochemistry, pharmacy or equivalent.
• 3+ years applicable experience in pharmaceutical analysis in analytical development or quality control.
• Expertise in applicable analytical techniques: Strong knowledge of HPLC, GC, Uv-Vis spectrophotometry, gel electrophoresis, gravimetry, volumetry, and titrimetry.. Working knowledge of cell-based assays and techniques a plus.
• Ability to multi-task and also be able to work on variety of experiments and studies in a team-based environment, preefereblay with a high level of independence.
• Good oral and written communication skills desired.
• Knowledge of cGMP compliance necessary.
• Knowledge of drug development and regulatory affairs a plus.