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About the Role
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
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 ...
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