Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Office

Job Description

Join Thermo Fisher Scientific in Monza as an QC Documentation Specialist and be an outstanding part of our world-class team! This is an outstanding opportunity to contribute to our mission of improving health, safety, and cleanliness through our innovative technologies and pharmaceutical services.

Job Responsibilities:

As a QC Documentation Specialist, you will play a crucial role in upholding our exceptionally high standards of quality and accuracy. You will be responsible for ensuring that all documentation processes are flawless and strictly adhere to company protocols. Your main tasks will include:

Perform a variety of tasks to support the efficient functioning of the organizationCollaborate with cross-functional teams to achieve departmental objectivesMaintain accurate records of activities and assist in data analysisFollow strictly defined protocols and procedures to ensure compliance with regulatory standardsDetermine and implement improvements to optimize workflows and processes

Requirements:High school diploma or equivalent experience will be considered.Proven ability to work effectively in a team environmentExcellent communication and organizational skillsStrong attention to detail and ability to multitaskBasic computer proficiency