Associate Principal Scientist, Downstream Vaccines And Advanced Biotechnologies Process R&d

539

West Point, PA, USA
$139,600.00 - $219,700.00; bonus/equity: annual bo...
Hybrid
Downstream process design and development
Recombinant protein purification
Chromatography and filtration unit operations
The Vaccines and Advanced Biotechnologies (VAX) Process R&D team is responsible for the development and clinical manufacturing of Drug Substance and Drug Product Intermediates for the vaccine and advanced therapy pipeline

Job Summary

  • The Vaccines and Advanced Biotechnologies (VAX) Process R&D team is responsible for the development and clinical manufacturing of Drug Substance and Drug Product Intermediates for the vaccine and advanced therapy pipeline.
  • The Associate Principal Scientist will provide scientific/technical leadership for a downstream/bio-purification process development team and be a critical member of cross-functional program/project teams.
  • The successful candidate will be eligible for annual bonus and long-term incentive, if applicable, and a comprehensive package of benefits including medical, dental, vision, and retirement benefits.

Matching Summary

The Vaccines and Advanced Biotechnologies (VAX) Process R&D team is responsible for the development and clinical manufacturing of Drug Substance and Drug Product Intermediates for the vaccine and advanced therapy pipeline.

Salary

$139,600.00 - $219,700.00; Bonus/Equity: Annual bonus and long-term incentive, if applicable; Benefits: Comprehensive package including medical, dental, vision, 401(k), paid holidays, vacation, sick days

Skills & Requirements

Must-have

  • Downstream process design and development
  • Recombinant protein purification
  • Chromatography and filtration unit operations
  • Biomolecule conjugation techniques
  • cGMP manufacturing understanding
  • Statistical design of experiments (DOE)

Nice-to-have

  • Innovative and highly motivated
  • Team-focused environment
  • Flexibility in responding to changing priorities
  • Mentoring junior staff
  • Authoring and reviewing CMC regulatory documentation

Key Requirements

  • BS/MS/PhD in engineering or biological sciences
  • 7+ years experience (BS), 5+ years (MS), or 3+ years (PhD)
  • Strong scientific and hands-on understanding of downstream unit operations
  • At least 5 years hands-on experience in downstream process optimization
  • Prior experience with statistical design of experiments (DOE)
  • Strong understanding of cGMP manufacturing

Work Rights

Not specified

Tailored Resume

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