The Role
The Sr Engineer will handle engineering practices in pharmaceutical production, including technical writing and vendor management while ensuring compliance with cGMP procedures and validation practices.
Summary Generated by Built In
• Excellent written and verbal communication skills
• Technical writing experience
• Working knowledge and experience with cGMP procedures and engineering practices on pharmaceutical/biotech production processes, facilities, and equipment.
• Experience with QRAES, Change cControl, non conformance, corrective and preventative actions, and validation practices.
• Experience with Maximo
• Capable of working and/or submitting Purchase Orders (PO)
• Experience working and escorting vendors
• Capable of handling multiple tasks, projects and/or priorities at the same time
• Independent, self-motivated, organized, able to multi-task in project environments, and skilled in communication, facilitation, and collaboration
• Work schedule flexibility as required to support 24/7 operations, requiring occasional after-hours engineering coverage.
Requirements
-Doctorate OR Masters + 2 years of Engineering experience OR
-Bachelors in Engineering + 4 years of Engineering experience.
8 hrs shift (1st)
Skills Required
- Doctorate or Masters + 2 years of Engineering experience or Bachelors in Engineering + 4 years of Engineering experience
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The Company
What We Do
ISPV Inc. is a Life Science company that leads Productivity & Validation projects for the Pharmaceutical and Food industries.
