Job Description Must have the following expertise; • 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 change control, 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 Shift, Education Field & Years of experience; Doctorate degree OR Master's degree and 3 years of Engineering experience Alternatively, a Bachelor's degree in Engineering and 5 years of Engineering experience.
8 hrs shift | 1st shift Requirements • 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 change control, nonconformance, 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.