Work Schedule
Standard (Mon-Fri)Environmental Conditions
Adherence to all Good Manufacturing Practices (GMP) Safety Standards OfficeJob Description
Main responsibilities:
Assure the execution of the validation projects within the timeline and the modality defined upon the priorities by the site management.
Edit and review validation documents (specification documents risk analysis and validation protocols) in agreement with the site procedures.
Work with other sites functions and external contractors to complete the validation tasks in agreement to the High Quality Standard
Define standards to ensure the validation of the computerized system according to the local and corporate guidelines.
Issue and update the local procedures aligned to the guideline and the corporate standards
Coordinate contractors and suppliers for the completion of the validation activities.
Competencies:
Computer Science/Scientific Degrees or equivalent experience
GMP/GAMP knowledge
Computer Systems validation guidelines
Word Excel MS Project
Previous experience in information systems validation
Hybrid site/remote work offered.
As one team of 100000 colleagues we share a common set of values - Integrity Intensity Innovation and Involvement - working together to accelerate research tackle complex scientific challenges drive technological innovation and support patients in need. #StartYourStory at Thermo Fisher Scientific where diverse experiences backgrounds and perspectives are valued.
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race color religion sex sexual orientation gender identity national origin protected veteran status disability or any other legally protected status.
Required Experience:
IC
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