Process Development Scientist – Commercial Support

Amgen Inc. (IR); Juncos (PR); On-site; USD 120,000 - 160,000; Full time

Benefits offered by this job

Retirement and Savings Plan

Stock-based long-term incentives

Award-winning time-off plans

Flexible work models

Job summary

Amgen Inc. in United States is seeking a Process Development Scientist – Commercial Support to help monitor and improve parenteral manufacturing processes. You will support technology transfers, investigations, and data-driven initiatives that ensure reliable production of life-changing therapies.

The role requires strong science background, cross-functional collaboration, and experience with regulatory documentation and cGMP expectations. A bilingual English/Spanish capability is valued.

Qualifications

• PhD or MS with relevant process development experience.
• Experience in biopharmaceutical manufacturing and formulation a plus.
• Regulatory and cGMP understanding preferred.
• Strong analytical and communication skills.

Responsibilities

• Support process monitoring and improvement initiatives for Formulation and aseptic Drug Product.
• Assist deviations investigations, RCA, and CAPA implementations.
• Prepare technical documents, protocols, reports and regulatory-support materials.
• Collaborate with Manufacturing, Quality and Engineering teams on projects.
• Perform data analysis and provide technical conclusions to teams.
• Ensure compliance with safety, quality, and regulatory requirements.

Skills

JMP software

Data analysis

Root cause analysis

Cross-functional collaboration

Scientific writing

Presentation skills

Technical writing

Problem solving

Team collaboration

English/Spanish bilingual

Education

PhD in Life Sciences/related field

MS in Life Sciences with 2+ years experience

BS in Science with 4+ years experience

Tools

JMP

Job description

Amgen Inc. in United States is seeking a Process Development Scientist – Commercial Support to help monitor and improve parenteral manufacturing processes. You will support technology transfers, investigations, and data-driven initiatives that ensure reliable production of life-changing therapies.

The role requires strong science background, cross-functional collaboration, and experience with regulatory documentation and cGMP expectations. A bilingual English/Spanish capability is valued.