Principal Scientist, Analytical Research & Development (NJ) (FullTime)

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Design and conduct experiments independently. Develop/validate analytical methods, perform physicochemical studies. Provide guidance to junior analysts working in the laboratory. Provide secondary review of data, results, etc. Maintain analytical instrumentation and associated documentation such as logbooks, etc. Attend conferences, symposia and meetings relevant to analytical chemistry, the pharmaceutical industry, and the Eyetech franchise. Conduct experiments and studies in a consistent state of cGMP compliance. Prepare scientific reports and regulatory documentation for inclusion in worldwide regulatory submission. Advise management of applicable developments in the fields of pharmaceutical analytical chemistry as appropriate. Keep current with field of analytical chemistry through conferences and reading of scientific literature. Communicate with Eyetech alliance partners and contract research organizations. Travel and represent company when appropriate.

Qualifications

• BA/BS, MS, Ph.D. in chemistry, biochemistry, pharmacy or equivalent (degree offset by number of years experience).
• 12+ (BS), 8+ (MS), 5+ (Ph.D.) years experience in pharmaceutical analysis.
• Expertise in applicable analytical techniques: Solid knowledge of HPLC, GC, Uv-Vis spectrophotometry, gel electrophoresis. 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.
• Good oral and written communication skills desired.
• Knowledge of drug development, cGMP compliance necessary. Some regulatory affairs knowledge a plus.