Pharmaceutical Development Specialist

2 weeks ago


Reston, Virginia, United States Randstad Life Sciences US Full time

Job Details:

Chemist II in a Large Materials Science and Analytical Chemistry Laboratory

12-Month Contract

General Shift

Job Summary:

This role is based in a state-of-the-art laboratory in Maple Grove, MN. As a key member of an analytical pharma team, you will provide critical support to the development and analysis of pharmaceutical products. Collaborate with R&D to develop, validate, and transfer new analytical methods and technologies to be implemented in a QC Lab.

Key Responsibilities:

  • Develop and own method development activities for pharmaceutical analysis methods, including OOS investigations, experimental plans, and technical reports.
  • Assist in the development and validation of new methods/technologies for pharmaceutical analysis, utilizing liquid chromatography, gas chromatography, and other analytical techniques as needed.
  • Write method transfer/validation protocols/reports and execute method transfer and validation studies.
  • Train QC technicians on new methods/technologies and source new equipment, perform qualifications, and write protocols, final reports, SOP's, and technical documents.
  • Lead special projects, write new procedures, and work plans for tests, and provide guidance in specialized analytical technologies.
  • Advise and direct other analytical technicians on work assignments and training, and evaluate new analytical technologies for application and added value in BSC operations.
  • Maintain compliance with all quality requirements by building quality into all aspects of work.

Requirements:

  • 2-4 years of experience with a BS or 0-2 years with an MS
  • Experience in cGMP/GLP laboratory
  • Experience with Waters Empower and MassHunter
  • HPLC and/or GC experience


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