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Analytical R&D, Vice President

Job Description

Edenbridge Pharmaceuticals is seeking an individual to join the Company leadership and contribute broadly to the Company's growth and success. This is a unique opportunity for an individual to join a growing specialty pharmaceutical company in Parsippany, New Jersey, with full responsibility over the Company's analytical R&D operations. The successful candidate will:

  • Work closely with the Company's CSO, Senior VP of Scientific Affairs, and the entire product development & commercialization teams on matters related to analytical chemistry.
  • Be the analytical subject matter expert and representative for the Company capable of communicating effectively with third party laboratories, planning the scope of all analytical work, developing and/or adapting analytical methodology, and executing all aspects of product testing in support of pharmaceutical product.
  • Control and manage all laboratory operations related to analytical chemistry.
  • Must be comfortable working in an independent start-up atmosphere.
  • Troubleshoot and solve analytical problems as they arise during analytical method development, transfer, and validation.
  • Establish effective relationships with third party contract development and manufacturing organizations to enable effective method transfers.
  • Recommend and facilitate the introduction of relevant technologies needed to support the formulation development function.
  • Qualifications

  • PhD analytical or physical chemist with 15+ years of relevant generic pharmaceutical industry analytical chemistry experience across various finished dosage forms.
  • Strong leadership skills capable of guiding internal colleagues and achieving project goals.
  • Excellent communication and interpersonal skills, particularly with third party partners.
  • Must be comfortable working within the lab setting and knowledgeable about the requirements of establishing and managing an analytical laboratory.
  • Key expertise must fall in the areas of HPLC and GC with knowledge of XRPD, HPLC-MS, GC-MS, and interpretive spectroscopic skills, including Elemental Analysis and NMR.
  • Demonstrated ability to effectively review and edit analytical documentation.
  • Writing skills consistent with the ability to prepare concise, timely, and accurate reports.
  • Extensive experience with US FDA regulated pharmaceutical development.

Qualified candidates should submit their resumes directly to careers2@edenbridgepharma.com.