( "ROOT CAUSE" ) AND ( VALIDAT* ) AND ( CGMP OR "CURRENT GOOD MANUFACTURING PRACTICE" OR GMP OR "GOOD MANUFACTURING PRACTICE" ) AND ( PROTOCOLS OR "REPORTS NOT SANOFI" ) AND ( EQUIPMENTS OR PROCESS ) AND ( PHARMACEUTICALS OR BIOPHARMACEUTICALS OR "BIO PHA
Job Title: Validation Specialist
Location: Swiftwater, PA
Duration: 4 Months with possible extension
Client has openings to support validation activities at Swiftwater site. The Validation Specialist will be responsible for generating development / validation protocols and reports, and analyzing data for adherence to established acceptance criteria.
Skills, 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 establishworking relationships withother support and production areasin 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.