Senior Scientist, Process Development – Drug Product

Amgen SA; Thousand Oaks (CA); Hybride; USD 150 000 - 190 000; Plein temps

Avantages offerts par ce poste

Retirement plan

Medical, dental, vision benefits

Bonus program

Stock-based incentives

Paid time off

Résumé du poste

Amgen seeks a Process Development Senior Scientist to join the Drug Product Team (DPT). You will lead experimental design (DOE) strategies and execute development programs for pivotal and commercial-ready products.

You will collaborate across Drug Substance Technologies, Attribute Sciences, QA, Regulatory, Supply Chain, Contract Manufacturing, PK/PD, and Biostatistics to advance oral solid dosage forms and related technologies, contributing to publication-ready research.

Qualifications

• Doctorate or Master’s with scientific experience or Bachelor’s with scientific experience as required by the posting.
• Ph.D. in a relevant scientific field such as Organic Chemistry, Physical Chemistry, Chemical Engineering, Materials Sciences, or Pharmaceutical Sciences.

Responsabilités

• Provide creative DOE strategies and execute development of pivotal and commercial ready programs.
• Collaborate across multiple functions including Drug Substance Technologies, Attribute Sciences, QA, Regulatory Affairs, Supply Chain, Contract Manufacturing, PK/PD, Clinical Development, and Biostatistics.
• Design and execute experiments and summarize results in technical documents and regulatory filings.

Connaissances

Scientific experience

Cross-functional collaboration

Formation

Ph.D. in Organic Chemistry / Physical Chemistry / Chemical Engineering / Materials Sciences / Pharmaceutical Sciences

Master’s + 2 years of Scientific experience

Bachelor’s + 4 years of Scientific experience

Outils

XRPD

DSC

TGA

SEM

Description du poste

Amgen seeks a Process Development Senior Scientist to join the Drug Product Team (DPT). You will lead experimental design (DOE) strategies and execute development programs for pivotal and commercial-ready products.

You will collaborate across Drug Substance Technologies, Attribute Sciences, QA, Regulatory, Supply Chain, Contract Manufacturing, PK/PD, and Biostatistics to advance oral solid dosage forms and related technologies, contributing to publication-ready research.