Process Development Scientist II

at  Frederick National Laboratory for Cancer Research

Frederick, Maryland, USA - 00000

Start DateExpiry DateSalaryPosted OnExperienceSkillsTelecommuteSponsor Visa
Immediate23 Feb, 2022Not Specified23 Nov, 2021N/AAseptic Technique,Vector,Addition,Molecular Biology,Design,Higher Education Accreditation,Assay Development,Viruses,Production ExperienceNoNo
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Description:

POSITION DESCRIPTION:

The Frederick National Laboratory is a Federally Funded Research and Development Center (FFRDC) sponsored by the National Cancer Institute (NCI) and operated by Leidos Biomedical Research, Inc. The lab addresses some of the most urgent and intractable problems in the biomedical sciences in cancer and AIDS, drug development and first-in-human clinical trials, applications of nanotechnology in medicine, and rapid response to emerging threats of infectious diseases.
Accountability, Compassion, Collaboration, Dedication, Integrity, and Versatility; it’s the FNL way.

PROGRAM DESCRIPTION

The Biopharmaceutical Development Program (BDP) of Leidos Biomedical Research, Inc. supports the National Cancer Institute (NCI) and other government agencies through the development of novel agents for first-in-man clinical studies.

TO BE CONSIDERED FOR THIS POSITION, YOU MUST MINIMALLY MEET THE KNOWLEDGE, SKILLS, AND ABILITIES LISTED BELOW:

  • Possession of a PhD degree from an accredited college or university according to the Council for Higher Education Accreditation (CHEA) or eight (8) years of related experience. Foreign degrees must be evaluated for U.S. equivalency
  • In addition to the educational requirements, a minimum of two (2) years of experience with recombinant proteins or viruses in an academic or industrial setting
  • Assay Development for viral and recombinant protein products
  • Expert in aseptic technique
  • Ability to obtain and maintain a security clearance

CANDIDATES WITH THESE DESIRED SKILLS WILL BE GIVEN PREFERENTIAL CONSIDERATION:

  • Protein and/or virus production experience is preferred
  • Molecular biology and vector design
  • Ability to work collaboratively in a multi-disciplinary environment

How To Apply:

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Responsibilities:

  • Design, optimize, and characterize upstream and downstream processes for the manufacture of recombinant proteins and viruses for phase I/II clinical trials
  • Interpret analytical and process data and understand process implications
  • Maintain accurate records of experimental results, review, analysis and interpretations of experimental data
  • Make periodic presentations in group meetings, project team meetings, and in one-on-one situations
  • Prepare technical reports
  • Support technology transfer to in-house clinical manufacturing group


REQUIREMENT SUMMARY

Min:N/AMax:5.0 year(s)

Pharmaceuticals

Pharma / Biotech / Healthcare / Medical / R&D

Clinical Pharmacy

Graduate

Proficient

1

Frederick, MD, USA