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Engineer, Quality Engineering

Job in West Greenwich, Kent County, Rhode Island, 02817, USA
Listing for: Amgen
Full Time position
Listed on 2026-07-01
Job specializations:
  • Engineering
    Quality Engineering, Process Engineer, Validation Engineer, Manufacturing Engineer
Salary/Wage Range or Industry Benchmark: 70000 - 90000 USD Yearly USD 70000.00 90000.00 YEAR
Job Description & How to Apply Below
Location: West Greenwich

Join Amgen’s Mission of Serving Patients

At Amgen, if you feel like you’re part of something bigger, it’s because you are. Our shared mission—to serve patients living with serious illnesses—drives all that we do.

Since 1980, we’ve helped pioneer the world of biotechnology in our fight against the world’s toughest diseases. With our focus on four therapeutic areas—Oncology, Inflammation, General Medicine, and Rare Disease—we reach millions of patients each year. Amgen is advancing a broad and deep pipeline of medicines to treat cancer, heart disease, inflammatory conditions, rare diseases, and obesity and obesity‑related conditions. As a member of the Amgen team, you’ll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller, happier lives.

Our award‑winning culture is collaborative, innovative, and science‑based. If you have a passion for challenges and the opportunities that lie within them, you’ll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career.

Engineer I What You Will Do

Let’s do this. Let’s change the world. In this vital role you will report to the Senior Manager of the Engineering group. Working under direction, the position is responsible for providing process and equipment engineering support at the Amgen Rhode Island site.

Specific duties include:

  • Ensures the logical, detailed translation of design requirements and constraints into process equipment/system solutions. Assists with project definition by performing engineering studies and assessments for process equipment systems, clean utilities, and production facility improvements.
  • Provide technical support to commercial manufacturing as required.
  • Working closely with multiple teams, including manufacturing, engineering, utility operations, maintenance, quality assurance, and validation to implement operational improvements.
  • Troubleshoot and resolve equipment, automation or process issues in the field.
  • Apply LEAN methodology to ensure optimal and cost‑effective performance and reliability for process systems.
  • Develop, organize, analyze, and present results for operational issues and engineering projects of small scope and complexity.
  • Applying engineering principles to recommendation, design, and implementation of new equipment or system modifications.
  • Ownership of systems including development of job plans, preventative maintenance, and the evaluation of spare parts.
  • Communicating proactively with supervisor and support staff, highlighting issues and proposing solutions.
  • Ability to provide on‑call support coverage on weekends, on a rotating basis.
What We Expect Of You

We are all different, yet we all use our unique contributions to serve patients. The motivated professional we seek is a self‑starter with these qualifications.

Basic Qualifications
  • High school diploma / GED and 8 years of Engineering or Biotechnology experience.
  • Associate’s degree and 6 years of Engineering or Biotechnology experience.
  • Bachelor’s degree and 2 years of Engineering or Biotechnology experience.
  • Master’s degree.
Preferred Qualifications
  • Bachelor’s Degree or Master’s Degree in Chemical Engineering or related technical field.
  • 2+ years experience in engineering in a manufacturing support environment with at least 1 year experience in the Pharmaceutical or Biotechnology industries.
  • Downstream unit operation experience such as Chromatography or Tangential Flow Filtration desired.
  • Familiarity designing, fixing, and operating equipment used in protein purification including disposable technologies.
  • Experience with Tech Transfer, Process Design, and Commissioning & Qualification.
  • Direct experience with regulated environments (i.e., cGMP, OSHA, EPA) including detailed understanding of cGMPs.
  • Position requires excellent written and verbal communication skills and the ability to work with minimum direction.
  • Ability to apply analytical skills to evaluate and interpret problems using multiple sources of information.
  • Demonstrated ability to work in cross‑functional teams and embrace a team‑based culture.
  • Familiarity with designing and operating…
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