Duration: 12 months Contract

 

This is a fully onsite role with standard business hours and occasional overtime as needed.

1–2+ years of hands-on experience in a GMP-regulated environment





Description:

Nice to Have:

Experience working in an FDA-regulated environment

• Familiarity with maintenance management software (e.g., Maximo)


• Experience with 3D modeling tools such as SolidWorks or similar


• Strong technical writing skills
  
  
  
  Job Details:


• Position involves support of senior staff in the initiation, design, and delivery of projects, particularly for automation related scope.


• Employ basic engineering skills and practices to gather user requirements and translate them into technical documentation for execution by third party firms.


• Assist with project definition by performing ...