Preferred: 8+ years of pharmaceutical industry experience in an engineering role (5+ years with CIP)

Primary Skills

· Support CIP troubleshooting efforts as a subject matter expert (SME)

· Support commissioning, qualification, and validation (CQV) team activities (reviewing protocols, reviewing SOPs, contacting vendors for information, equipment troubleshooting, etc.)

· Drive resolution of CQV testing issues and findings (organize meetings, generate technical justifications, etc.)

· Monitor system punch list and drive punches to closure

· Maintain highlighted CIP flow path drawings

· Support investigations associated with instrument out of tolerance events

· Generate Trackwise change controls and drive them to closure

· Generate preventative maintenance (PM) plans

· Identify spare parts based on vendor documentation

Preferred (but not required skills)

· DeltaV troubleshooting skills (need to be able to direct the automation team to what needs to be fixed / changed)

· Washer and/or autoclave experience