Thermo Fisher Scientific Engineer III, Validation in Cincinnati, Ohio
Title: Engineer III, Validation
US - Ohio - Cincinnati
Division: Pharma Services Group
When you join us at Thermo Fisher Scientific, you’ll be part of a smart, driven team that shares your passion for exploration and discovery. With revenues of $22 billion and the largest investment in R&D in the industry, we give our people the resources and opportunities to make significant contributions to the world.
Duties & Responsibilities:
This position serves as the subject matter expert on cleaning validation policy and procedures at the Cincinnati site. Authors all protocols related to the cleaning of equipment. Reviews and organize swab results. Authors cleaning validation reports. Responsible for the Annual Monitoring program used to monitor the effectiveness of cleaning procedures at the Cincinnati site. May be asked to participate as the SME during customer and regulatory audits. Job responsibilities are similar, although not routine. Job tasks are clearly defined but timing or priority decisions must be made sometimes where competing demands must be balanced to meet timelines/schedule.
2 to 3 years’ experience in Validation within the Pharmaceutical industry
Excellent computer skills (Microsoft Word, Excel, Power Point)
Superior writing skills, strong accuracy, attention to detail, and technical knowledge
Experience with a variety of pharmaceutical manufacturing equipment
B.S. in Engineering discipline (Chemical, Mechanical, or related).
About Thermo Fisher Scientific
At Thermo Fisher Scientific, each one of our 70,000 extraordinary minds has a unique story to tell. Join us and contribute to our singular mission—enabling our customers to make the world healthier, cleaner and safer.
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