Process Development Scientist, Cell Sciences & Engineering

Amgen SA; Juncos (PR); On-site; USD 110,000 - 160,000; Full time

Benefits offered by this job

Retirement plan

Medical/dental/vision coverage

Life & disability insurance

Discretionary bonus

Stock-based incentives

Paid time off

Flexible work models

Job summary

Amgen is seeking a Process Development Scientist to support Drug Substance Cell Sciences and Engineering. You will contribute to process development, technology transfer, and investigations that ensure reliable manufacturing of life-changing therapies.

The role emphasizes data-driven problem solving, cross-functional teamwork, and adherence to cGMP standards while advancing medicines for patients globally.

Qualifications

• Doctorate or Master’s with relevant experience in process development or manufacturing support.
• Experience in biopharmaceutical process development and technology transfer is preferred.
• Familiarity with cGMP and regulated manufacturing environments.

Responsibilities

• Support process improvement initiatives, technology transfers, and data-driven solutions for Drug Substance manufacturing.
• Assist with deviations investigations, root cause analysis, and corrective action implementation.
• Develop and troubleshoot scientific methods and protocols for project needs.
• Prepare technical documents, reports, and regulatory-support materials.
• Collaborate with Manufacturing, Quality, Engineering, and Process Development teams.
• Present data analyses and recommendations to cross-functional teams.

Skills

Data analysis

Statistical analysis

Technical writing

Cross-functional collaboration

Problem solving

Bilingual English/Spanish

Education

Doctorate degree

Master’s degree + 2 years experience

Bachelor’s degree + 4 years experience

Tools

JMP

Job description

Amgen is seeking a Process Development Scientist to support Drug Substance Cell Sciences and Engineering. You will contribute to process development, technology transfer, and investigations that ensure reliable manufacturing of life-changing therapies.

The role emphasizes data-driven problem solving, cross-functional teamwork, and adherence to cGMP standards while advancing medicines for patients globally.