Engineer - (Downstream, Purification)

**Engineer I (Downstream, Purification)**

Singapore

**HOW MIGHT YOU DEFY IMAGINATION?**

Amgen is one of the world’s leading independent biotechnology companies. For over 4 decades, Amgen has pioneered biotechnology breakthroughs, to bring state-of-the-art medicines from laboratory to the patient. Amgen has not only discovered and developed innovative human therapeutics, but has invested in cutting edge manufacturing capability and support services to deliver these exciting therapies to medical teams around the world. Japan and Asia Pacific (JAPAC) is the fastest growing region in Amgen. Now we are hiring an **Engineer I (Downstream, Purification) **in **Singapore**.

**Engineer I (Downstream, Purification)**:
**Live**:
**What you will do**
- Applies expertise in the successful coordination of multiple, complex, non-routine activities including facility start up, process qualification through to regulatory approval, process performance monitoring, floor support, troubleshooting of unit operations and technology transfer of new processes.
- Must have strong knowledge and understanding of purification processes
- Compile and analyze process data using tools such as excel, minitab, JMP, SIMCA
- Verify data in technical reports, spreadsheets and regulatory filings
- Author technical protocols, technical assessments and product impact assessments
- Utilize strong written and verbal communication skills in technical writing and presentations
- Participate/lead in teams and collaborate cross-functionally with representatives from other functions and sites to transfer and support drug substance manufacturing processes
- Organize and conduct meetings. Actively creates, generates, and presents data/conclusions at internal and cross functional meetings
- Be part of digitation of process tech transfer

**Win**:
**What we expect of you**:
**Qualifications**:
**Win**:
**What we expect of you**:
**Qualifications**:

- Master’s degree OR
- Bachelor’s degree and 2 years of directly related experience OR
- Associate’s degree and/or 6 years of directly related experience OR
- High school diploma / GED and 8 years of directly related experience
- Experience working with commercial manufacture of biologics using single use technology
- Experience related to upstream process development technology transfer, scale-up and ongoing manufacturing of biologics (cGMP). This includes technical support for nonconformance investigations and other commercial support activities.
- Possess basic understanding of regulatory and cGMP requirements
- Able to elevate relevant issues to project lead and line management
- Independently motivated but also work well in team environment
- Excellent written and verbal communication

**Thrive**:
**What you can expect of us**

As we work to develop treatments that take care of others, so we work to care for our teammates’ professional and personal growth and well-being.
- Vast opportunities to learn and move up and across our global organization
- Diverse and inclusive community of belonging, where teammates are empowered to bring ideas to the table and act
- Generous Total Rewards Plan comprising health, finance and wealth, work/life balance, and career benefits

**for a career that defies imagination**:
In our quest to serve patients above all else, Amgen is the first to imagine, and the last to doubt. Join us.

**Equal Opportunity Statement**:
Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status.