Career Category
OperationsJob Description
HOW MIGHT YOU DEFY IMAGINATION?
You’ve earned your degree. How will you use that achievement to reach your goals? Do more with the knowledge you’ve worked hard to acquire and the passion you already have. At Amgen, our shared mission—to serve patients—drives all that we do. It is key to our becoming one of the world’s leading biotechnology companies, reaching over 10 million patients worldwide. Become the professional you are meant to be in this meaningful role.
Job Posting Title
Senior Engineer – Drug Substance Process Engineering
Location (City)
Cambridge, MA based team but flexible or remote work is an option
Live
What you will do
Let’s do this. Let’s change the world. In this vital role you will
apply process engineering knowledge to support development, scale-up of clinical and commercial purification processes as well as technology transfer.
Roles and responsibilities
Provide on-the-floor technical support when required for successful scale-up or transfer of process technology
Apply strong written and verbal communication skills in technical writing and presentations
Represent process development and collaborate with other functions such as Process Development, Manufacturing, Quality, Validation and Regulatory
Design and perform experiments in the lab/pilot-plant to resolve technical issues observed during scale-up to or manufacturing at large scale when required per project
Win
What we expect of you
We are all different, yet we all use our unique contributions to serve patients. The skilled professional we seek is a collaborative partner with these qualifications.
Basic Qualifications
Doctorate degree
Or
Master’s degree & 3+ years of directly related experience
Or
Bachelor’s degree & 5+ years of directly related experience
OR
High school diploma / GED and 12 years of directly related experience
Preferred Qualifications
Doctorates degree & 1+ year of direct experience, Master's degree & 4 years of experience, Bachelor's degree & 6 years of direct experience strongly preferred
Experience related to upstream (cell culture) / downstream (purification) process development/characterization, technology transfer, scale-up and manufacturing of biologics (cGMP) This includes technical support for nonconformance investigations and other clinical/commercial support activities
Experience in process scale-up and technology transfer from laboratory to pilot and/or manufacturing scale
Experience working directly with commercial manufacture of biologics using single use technology
Experience working with contract manufacturers
Possess sophisticated understanding of regulatory and cGMP requirements
Able to apply engineering principles and statistical analysis, including design of experiments, in-order to tackle processing issues and evaluate opportunities for process improvements
Experience in the analysis of data generated from a variety of analytical techniques
Able to handle project resources and elevate relevant issues to project lead and line management
Independently motivated but also work well in a team environment
Excellent written & verbal communication
Thrive
Some of the vast rewards of working here
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.
Full support and career-development resources to expand your skills, enhance your expertise, and maximize your potential along your career journey
A 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—with compensation and benefits rated above 4 stars (out of 5) on Glassdoor
Apply now
for a career that defies imagination
Objects in your future are closer than they appear. Join us.
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