Production Quality Specialist - fixed term (RED PROGRAM)

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

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.

The Resources Empowerment and Development (R.E.D.) Program is designed for people who seek a performance-based culture that is built on meritocracy - ambitious, hard-working, passionate employees who deliver results will be rewarded.

This program will start in Ferentino and foresees secondments in various functional groups (Manufacturing, Quality, Supply Chain etc.) where selected candidates will experience accelerated career opportunities throughout job rotations, having the chance to be part of different teams.

The ultimate goal is that of creating formed professionals to work in key teams: Production Quality Specialist.

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, preferred Fields of Study: Chemistry, Biology, Engineering, Life Sciences, or related scientific field

• Additional relevant certifications (e.g. ISO auditor, Six Sigma) are advantageous

• Fluency in English required; additional language skills beneficial

• 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

• Commitment to maintaining a quality-focused culture and driving continuous improvement

• Collaborate with the Quality System Department to review SOPs

• Conduct and manage departmental training

• Prepare and present compliance documents and procedures

• Manage internal, customer, and regulatory audits

• Support continuous improvement initiatives

• Provide documentary support to the production department

• Proven ability to review and approve GMP documentation, batch records, and quality records