Added
8 days ago
Type
Full time
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gmp regulatory submissions ce hplc cmc
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๐Ÿ“‹ Description

  • Independently develop and apply capillary electrophoresis, and HPLC methods separation as well as
  • Develop, qualify, and transfer fit-for-purpose in-process control methods to QC
  • Provide technical support to QC testing occurring at internal and external GMP testing laboratories
  • Demonstrate the ability to resolve key project hurdles and assumptions by effectively utilizing
  • Publish research in peer-reviewed journals and present work at scientific conferences
  • Proactively seek out new information in the literature and incorporate this into individual

๐ŸŽฏ Requirements

  • PhD Degree and 0-4+ years or MS with 10+ years of experience within Biochemistry, Chemical
  • Possess thorough theoretical and practical understanding of own scientific discipline
  • Effective writer and communicator of research or other regulatory materials
  • Must have strong written and verbal communications skills

๐ŸŽ Benefits

  • Medical/dental/vision insurance
  • 401(k)
  • Paid time off (vacation, holidays, sick)
  • Eligible to participate in long-term incentive programs
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