This role will support validation activities at our Swiftwater site.
The Validation Specialist will be responsible for generating development / validation protocols and reports, and analyzing data for adherence to established acceptance criteria.
MS Office 2010, eDoc/GEODE+, Pharmaceutical Validation, Bio Pharma Validation, Validation execution,
Technical writing abilities and excellent time management.
Strong root cause analysis skills with cGMP experience.
To be able to establish working relationships with other support and production areas in order to gather all of the necessary information required.
Must be proficient in eDoc/GEODE+ with a working knowledge of templates, workflows and approval process Proficient in MS Word, Excel, Powerpoint and Outlook Interact well with a diverse group of individuals Self motivated and willing to be pro-active in resolving issues.
Excellent Verbal and written communication skills. Ability to work in a team environment.
BS/MS in Engineering, Life Science or Physical Science
Source: Job Diva – Job Listing