Bioconjugation Process Development VP — Lead Scale to GMP

AL Solutions

United States

On-site

USD 240,000 - 360,000

Full time

31 hours ago
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Benefits offered by this job

Relocation assistance

Job summary

AL Solutions in Philadelphia is seeking a Vice President of Bioconjugation Process Development. This senior role will steer the bioconjugation development strategy, manage a skilled team, and drive scale-up and technology transfer into GMP manufacturing.

The candidate will lead discovery and development activities, oversee downstream purification, analytical characterization and process transfer, and act as a senior technical trusted advisor to clients.

Qualifications

  • PhD or BS/MS with extensive bioconjugation experience in biotech/biopharma/CDMO.
  • Experience leading bioconjugation development teams and training scientists.
  • Strong track record transferring processes into GMP manufacturing.

Responsibilities

  • Define and lead strategy for bioconjugation process development.
  • Oversee conjugation, purification, characterization and scale-up for GMP readiness.
  • Establish critical parameters, QA attributes, control strategies and development plans.
  • Own transfer readiness and documentation for GMP manufacturing.
  • Provide senior scientific oversight during GMP campaigns and troubleshoot issues.
  • Build and mentor scientists and leaders within the Bioconjugation group.
  • Represent development strategies to clients and contribute to proposals.

Skills

Bioconjugation process development
Leadership
Client presentations

Education

PhD in Chemistry/Biochemistry/Chemical Engineering/Bioengineering/Bioprocessing or related
MS/BS in Chemistry/Biochemistry/Chemical Engineering/Bioengineering/Bioprocessing or related

Tools

GMP knowledge
Process transfer

Job description

AL Solutions in Philadelphia is seeking a Vice President of Bioconjugation Process Development. This senior role will steer the bioconjugation development strategy, manage a skilled team, and drive scale-up and technology transfer into GMP manufacturing.

The candidate will lead discovery and development activities, oversee downstream purification, analytical characterization and process transfer, and act as a senior technical trusted advisor to clients.

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