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Sr. Associate

West Greenwich, RI
Top 3 Must Have Skill Sets:
  • BS Degree in Engineering (Mechanical, Civil, Electrical, Computer, Biomedical, etc.)
  • Mechanical Design and Modeling Experience
  • Candidates with some combination of HPLC, GC, GC/MS, ICP/MS (Preferred and must be ready to explain during an interview)
  • Strong communication and writing skills

Day to Day Responsibilities:
  • The Sr. Associate, working with more senior staff, will provide process monitoring, troubleshooting support and systems analysis of drug substance manufacturing operations for Amgen’s global manufacturing network and contract manufacturing sites.
  • Responsibilities will also include process monitoring for the Drug Substance Manufacturing network, collaborate with other technical staff for implementation of process improvements, and use data analytical techniques (including multivariate data analysis) to identify signals in process performance.

Summary
  • As the candidate for this largely laboratory-based position, you will be responsible for driving cutting-edge analytical support and technology development impacting process and product development teams.
  • You will work cross-functionally and across Process Development sites as you use analytical science to help drive efficient development and scalable understanding of processes and products.

Minimum Basic Qualifications
  • BS Degree in Engineering (Mechanical, Civil, Electrical, Computer, Biomedical, etc.)
  • Min 2 years' experience performing analytical testing.
  • Experience with a broad array of chromatographic and spectroscopic techniques. Candidates with some combination of HPLC, GC, GC/MS, ICP/MS
  • Demonstrate independence and ability to produce quality GMP results under minimal direction
  • Generate complete, accurate, and concise documentation using electronic systems and laboratory notebook per GMP
  • High energy individual who can multi-task and handle a fast-pace, dynamic work environment
  • Operate specialized laboratory equipment and instrumentation in a GMP environment
  • Perform general laboratory housekeeping activities
  • Complete training on assigned tasks
  • Comply with safety guidelines and site specific procedures which include but is not limited to, the maintenance of training records, laboratory documentation, written procedures, building monitoring systems and laboratory log books
           "This posting is for Contingent Worker, not an FTE"
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