Work Schedule
Standard (Mon-Fri)Environmental Conditions
Adherence to all Good Manufacturing Practices (GMP) Safety Standards, OfficeJob 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 organization
- Collaborate with cross-functional teams to achieve departmental objectives
- Maintain accurate records of activities and assist in data analysis
- Follow strictly defined protocols and procedures to ensure compliance with regulatory standards
- Determine 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 environment
- Excellent communication and organizational skills
- Strong attention to detail and ability to multitask
- Basic computer proficiency
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