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Senior Associate IS Engineer

Employer
Amgen
Location
West Greenwich, RI
Start date
May 24, 2022

Job Details

HOW MIGHT YOU DEFY IMAGINATION?

Youve earned your degree. How will you use that achievement to reach your goals? Do more with the knowledge youve worked hard to acquire and the passion you already have. At Amgen, our shared missionto serve patientsdrives all that we do. It is key to our becoming one of the worlds leading biotechnology companies, reaching over 10 million patients worldwide. Become the professional you are meant to be in this meaningful role.

Senior Associate IS Engineer

Live

What you will do

The Senior Associate IS Engineer reports to the Sr. Manager of the Information Systems Team. The position is responsible for providing IS platform support at the Amgen Rhode Island site.

We are seeking a Senior Associate IS Engineer to join the Operations Information Systems team. The incumbent will be responsible for all activities related to managing and supporting IS/MFG platforms including system administration; as well as incorporating new technologies under the challenge of a sophisticated and constantly evolving technology landscape. The successful candidate for this position will be located at our Rhode Island West Greenwich manufacturing site and will collaborate with the Senior Manager of Information Systems.

  • System administration and maintenance of Rockwell, Siemens, and other utilities control platforms.
  • Collaborate with business partners and other software engineers to develop and deploy the latest, advanced technologies in support of product manufacturing optimization
  • Manage and/or support the execution of a varied portfolio of IS projects with appropriate portfolio planning, resource and risk management and financial management for the portfolio.
  • Work closely with the delivery and platform teams to ensure that the applications are aligned with standard city planning approved architectural and development guidelines
  • Support selected efforts to design, build, and develop rapid Proof-of-Concept (POC) automated solutions and services. Quickly and iteratively prove or disprove the concepts being considered.
  • Collaborate with business partners to understand how automation can improve workflow and productivity
  • Work closely with other business and IS Process Engineers to identify opportunities to stop inefficient practices, simplify business processes, and codify into automated solutions and platforms.
  • Experience in a GMP environment is required.
Basic QualificationsMasters degree

OR

Bachelors degree and 2 years of Engineering or Information Systems experience

OR

Associates degree and 6 years of Engineering or Information Systems experience

OR

High school diploma / GED and 8 years of Engineering or Information Systems experience

Win

What we expect of you

We seek is a self-starter with these qualifications:

  • BS or MS in computer science, engineering, information systems, or related field
  • Industry experience with utilities/manufacturing software development or management
  • Experience with Data analysis and reporting experience by using analytics, visualization and database technologies (OSISoft PI RtReports, Spotfire, Tableau)
  • Knowledge with several Industry 4.0 technologies is a plus including, but not limited to Process Modeling and Simulation, Data Driven Process Control, Internet of Things, Automated Warehouse solutions, and Automated Guided Vehicles. Some specific technologies and capabilities include:
  • Methods and technologies to support Manufacturing Data integrations (e.g. SQL, Web Services/messaging, data mapping)
  • Korber PAS|X, OSISoft PI, VeevaVault, iWAREHOUSE, VirTECS, Autodesk BIM 360
  • Hands-on experience with computerized systems including troubleshooting, reliability, and performance improvements
  • Experience with translating business requirements to technical requirements and recommend solutions for automation
  • Willing and able to learn new technologies at a rapid pace
  • Experience or solid understanding of current Good Manufacturing Practices (cGMP), 21CFR Part 11 regulations, change control, validation.
  • Experience with Process Design/Configuration and Commissioning
  • Experience with validation and change control methodology
  • Strong written and verbal communication skills and the ability to work with minimal direction.
Thrive

Some of the vast rewards of working here

As we work to develop treatments that take care of others, we also 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 Plancomprising health, finance and wealth, work/life balance, and career benefitswith 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.

careers.amgen.com


Join Us

If you're seeking a career where you can truly make a difference in the lives of others, a career where you can work at the absolute forefront of biotechnology with the top minds in the field, you'll find it at Amgen.

Amgen, a biotechnology pioneer, discovers, develops and delivers innovative human therapeutics. Our medicines have helped millions of patients in the fight against cancer, kidney disease, rheumatoid arthritis and other serious illnesses.

As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other but compete intensely to win. Together, we live the Amgen values as we continue advancing science to serve patients.

Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status.

We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.

Amgen requires all staff in the United States, Puerto Rico and Canada to be vaccinated from COVID 19 as a condition of employment. In accordance with applicable law, Amgen will provide reasonable accommodations to staff members who qualify on the basis of a medical reason or a sincerely held religious belief, practice, or observance. Such accommodation may not pose an undue hardship to Amgen, its operations, or its staff.

Company

We are all different, yet we have this in common: our mission to serve patients. This sense of shared purpose is key to our becoming one of the world’s leading biotechnology companies. It guides us as we continue to launch new medicines and reach millions of patients worldwide.

We live the mission.

We win together.

We thrive on continual challenge.

Our team of 22,000+ scientists and professionals worldwide bring distinct perspectives and experiences to all we do. We leverage our global talent to achieve together—to research, manufacture and deliver ever-better products and greater depth to our mission.

At Amgen, there is a strong correlation between our high level of diversity and performance. Because addressing issues with a wider range of perspectives and approaches leads to more creative problem-solving. Together, we’re transforming the promise of science and biotechnology into therapies that have the power to restore health.

Connect with us to explore how you can Win, Live, and Thrive at Amgen.

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Company info
Website
Phone
805-447-1000
Location
Corporate Headquarters
One Amgen Center Drive
Thousand Oaks
California
91320-1799
United States

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