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Principal Scientist- Bioconjugation Process Development

Company

NJ Bio, Inc.
Address New Jersey, United States
Employment type FULL_TIME
Salary
Category Research Services,Biotechnology Research,Pharmaceutical Manufacturing
Expires 2023-07-26
Posted at 10 months ago
Job Description

NJ Bio Inc. is a growing chemistry and biotech CRO with laboratories located in Princeton, NJ and Bristol, PA. NJ Bio offers competitive salary, great benefits, and significant growth opportunities within the organization. NJ Bio is constantly expanding its team and is looking for dedicated and talented individuals.

Principal Scientist- Bioconjugation Process Development will lead the process development and production of ADCs as part of a multi-disciplinary team to advance ADC development and provide on-floor GMP support of manufacturing.


Responsibilities:

  • Defining the approach to late-stage process characterization to define critical process parameters (CPPs) and processing ranges
  • Development and optimization of conjugation protocols utilizing novel chemistries and technologies
  • Lead bioconjugation process development for the CMC team and lead bioconjugation process development and technical transfer for manufacturing recombinant proteins.
  • Represent the bioconjugation development group as a member of multidisciplinary project teams
  • Development and optimization of conjugation protocols utilizing novel chemistries and technologies
  • Developing bioconjugation, purification, and UF/DF processes for use in first-in-human (FIH) GMP manufacturing of clinical candidates
  • Manage a team of bioconjugation scientists to meet project deliverables


Education, Experience and Skills:

  • Candidates with previous experience in the development of ADCs, including hands-on experience with the development of conjugation, purification, and UF/DF processes, are preferred
  • Candidates with good working knowledge of analytical techniques, including HIC-, SEC-, RP-HPLC, and capillary electrophoresis, are preferred
  • Candidate should have experience with cGMP manufacturing, preferably in bioconjugation
  • Qualified BS/MS candidates should have at least 15 years of industrial experience in a drug development setting
  • A Ph.D. in Biochemistry, Chemistry, or a related discipline with 10+ years of industrial experience is preferred
  • Proven ability to collaborate effectively within cross-functional teams
  • Subject Matter Expert in bioconjugation process development and manufacturing in support of CMC
  • Excellent analytical, communication, organizational, and presentation skills are essential