Quality Specialist

ThermoFisher Scientific; Monza; On-site; EUR 40,000 - 55,000; Full time

Job summary

Thermo Fisher Scientific invites applications for a Quality Specialist I to join our team in Monza, Italy. You will oversee quality across manufacturing, review GMP documentation, and support continuous improvement efforts in a collaborative environment.

Ideal candidates hold a Bachelor's degree, knowledge of GMPs, and strong documentation and analytical skills. English fluency is required; Italian language skills are a plus. This is a full-time on-site role with standard Mon-Fri hours.

Qualifications

• Bachelor's degree in a relevant field.
• Knowledge of GMP manufacturing environment and regulatory expectations.
• Experience reviewing GMP documentation, batch records, and quality records.

Responsibilities

• Ensure quality compliance across manufacturing operations.
• Provide essential quality oversight through documentation review and process monitoring.
• Collaborate with cross-functional teams to drive quality improvements and GMP compliance.

Skills

Quality oversight

Documentation

Analytical thinking

Communication skills

Cross-functional collaboration

Root cause analysis

Environmental monitoring

English proficiency

Education

Bachelor's Degree

Tools

Quality systems software

Microsoft Office

Job description

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office, Warehouse

Job Description

As part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world’s toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer.

DESCRIPTION:

Join our high-performing team at Thermo Fisher Scientific, where you'll ensure quality compliance across manufacturing operations while advancing our mission to make the world healthier, cleaner, and safer. As a Quality Specialist I, you'll provide essential quality oversight through detailed documentation review, process monitoring, and collaboration with cross-functional teams. You'll help maintain GMP compliance, investigate quality events, and drive continuous improvement initiatives while working in a collaborative environment focused on delivering life-changing products to our customers.

REQUIREMENTS:

• Bachelor's Degree required, no prior experience required, preferably in a GMP manufacturing environment
• Preferred Fields of Study: Chemistry, Biology, Engineering, Life Sciences, or related scientific field
• Additional relevant certifications (e.g. ISO auditor, Six Sigma) are advantageous
• Thorough knowledge of FDA, EMA, and international GMP regulations
• Proven ability to review and approve GMP documentation, batch records, and quality records
• Strong understanding of quality management systems and tools (e.g. CAPA, change control)
• Excellent documentation and technical writing skills
• Proficiency with quality systems software and Microsoft Office applications
• Strong analytical and problem-solving abilities with keen attention to detail
• Outstanding verbal and written communication skills
• Ability to work independently and collaborate effectively across functions
• Experience conducting quality investigations and root cause analysis
• Knowledge of environmental monitoring and contamination control principles
• Flexibility to work various shifts as needed to support manufacturing operations
• Ability to gown and work in controlled manufacturing environments when required
• Sound judgment and decision-making skills
• Commitment to maintaining a quality-focused culture and driving continuous improvement
• Fluency in English required; additional language skills beneficial

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.