Bioconjugation Process Development Lead (ADC)

Amgen; Thousand Oaks (CA); Sur place; USD 190 000 - 250 000; Plein temps

Avantages offerts par ce poste

Total Rewards Plan

Stock-based long-term incentives

Flexible work models

Retirement and savings plan

Résumé du poste

Amgen, located at the Thousand Oaks campus in California, seeks a Senior Principal Scientist in Bioconjugates to lead a diverse team and drive sustainable manufacturing processes for ADCs. You will guide process development, mentor staff, and advance technology from early to late-stage development.

The role requires deep expertise in bioconjugation, cGMP, and regulatory interactions, with a proven record of leadership and scientific innovation in pharma.

Qualifications

• PhD/PharmD/MD with relevant post-doc experience and 3+ years in science.
• Masters with 6+ years in pharma or related field.
• Bachelor’s with 8+ years scientific experience.

Responsabilités

• Lead a multidisciplinary team for bioconjugate manufacturing at all stages of clinical development.
• Drive bioconjugation technology innovation and process improvements.
• Support cGMP manufacturing and technology transfer to GMP facilities.
• Develop strategies for process understanding, modeling, and characterization.
• Ensure timely delivery of project milestones and regulatory documents.
• Serve as technical expert and mentor staff in bioconjugation.
• Collaborate cross-functionally to advance regulatory filings.

Connaissances

Bioconjugation process development

People leadership

Regulatory knowledge

Cross-functional collaboration

Industrialization of bioconjugation

Formation

PhD

PharmD

MD

Masters

Bachelor's

Outils

Bioconjugation techniques

ADC/HPAPI linker-payload synthesis

cGMP manufacturing

CMO tech transfer

Description du poste

Amgen, located at the Thousand Oaks campus in California, seeks a Senior Principal Scientist in Bioconjugates to lead a diverse team and drive sustainable manufacturing processes for ADCs. You will guide process development, mentor staff, and advance technology from early to late-stage development.

The role requires deep expertise in bioconjugation, cGMP, and regulatory interactions, with a proven record of leadership and scientific innovation in pharma.