Process Development Senior Scientist - Drug Product Technologies

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In this vital role you will join the Pre‑Pivotal Drug Product Technologies group, responsible for early‑stage drug product development across diverse modalities with a strong emphasis on antibody‑drug conjugates (ADCs), monoclonal antibodies, multispecifics, and other biologic modalities. The role involves designing and developing liquid and lyophilized formulations, evaluating critical quality attributes (CQAs), establishing robust, scalable fill/finish processes for complex biologic drug products, and authoring and supporting high‑quality regulatory submissions.

The ideal candidate will bring hands‑on experience in ADC drug product formulation and drug product process development, including a mechanistic understanding of linker‑payload attributes, stability/process‑relevant degradation pathways, and analytical strategies used to characterize ADC CQAs. This candidate will integrate formulation, analytical, and process data to guide product design, apply cutting‑edge technologies (including AI/ML), and collaborate cross‑functionally to deliver high‑quality, stable, and manufacturable drug products for clinical development in a fast‑paced environment.

• Work effectively in a fast‑paced, matrixed environment, collaborating across process development, research, regulatory, and manufacturing teams to advance programs and communicate technical recommendations to both scientific peers and leadership.
• Plan and execute formulation and fill/finish process studies for early‑stage programs.
• Develop and characterize liquid and lyophilized formulations for biologics, with particular emphasis on ADC drug product formulation, handling, and lab‑scale sterile filling.
• Build process understanding across unit operations to support scalable drug product development.
• Evaluate in‑use compatibility and drug product stability under clinical conditions.
• Investigate ADC‑ and biologics‑relevant CQAs (e.g., aggregation, fragmentation, drug‑to‑antibody ratio, free payload, charge/size variants, subvisible particles, surface interactions) to inform formulation and process design decisions.
• Leverage high‑throughput tools for formulation screening and processability assessments.
• Identify and address technology gaps impacting ADC stability, linker‑payload integrity, protein‑excipient interactions, and process‑related stress responses.
• Apply machine learning, AI, and data science to predictive modeling, workflow acceleration, and decision‑making.
• Ensure development approaches are phase‑appropriate, from discovery through clinical manufacturing.
• Author technical documents, control‑strategy inputs, risk assessments, IND/CTA regulatory sections, and tech transfer packages.
• Support internal and external technology transfer activities, including collaboration with CMOs/CDMOs, batch record review, process fit assessments, person‑in‑plant support, and troubleshooting during manufacturing campaigns.
• Present findings to internal/external stakeholders and participate in cross‑functional teams.

The scientific professional we seek is an individual with the following qualifications.

• Doctorate degree (PhD, PharmD, or MD) AND relevant post‑doc where applicable
• OR
• Masters degree and 3 years of scientific experience
• OR
• Bachelors degree and 5 years of scientific experience

• PhD in Pharmaceutics, Biotechnology, Biochemistry, or related field with 24 years of postdoc or industry experience.
• Proven experience in formulation development, stability testing, and fill/finish operations for biologics; direct ADC drug product formulation experience is strongly preferred.
• Demonstrated understanding of ADC drug product development considerations, including linker‑payload stability, drug‑to‑antibody ratio, free drug or payload degradation, quality attributes, and product/process comparability.
• Experience…