Investigation & Client Quality Specialist (Fixed
Pubblicato il 07-08-2026 - Thermo Fisher Scientific in Ferentino
**Work Schedule** Standard (Mon-Fri) **Environmental Conditions** Office Join Thermo Fisher Scientific to make a positive impact globally and help solve tough challenges like protecting the environment and finding cures for cancer. The Investigation & Client Quality Specialist: - Handless company functions to define the causes and implement the corrective action plan within the timeframes set out in technical agreements;
- Verifies, over time, the efficiency of corrective actions;
- Collaborates with colleagues in coordinating technical and management meetings with customers;
- Participates in customer visits and quality inspections (Audits) and internal and regulatory body quality inspections;
- Generates reports on quality events;
- Gives to the achievement of quality objectives for the part of their competence, and of the RFT, Deviation Rate, Past due, Ontime closure objectives;
- Supplies to the achievement of Business/customer objectives;
- Collaborates with Compliance colleagues in reviewing and drafting the Quality System SOPs that fall within the scope of the Quality Unit to which they belongs;
- Participates in the drafting of FMEAs;
- Deals with the drafting, archiving, distribution of controlled company documentation;
- Trains personnel involved in PDS/DPS quality activities;
- In accordance with the instructions and scheduling of activities by the manager, deals with drafting QATs and negotiating them with Customers, site QPs and the legal team.
- Covers the role of SME and QO contact for assigned projects, representing the quality figure of reference and support for Customers and internal departments in order to guarantee the success of projects and the manufacturing/disposition of GMP batches.
- Supports the team and other functions in ensuring full support for Readiness and BUs processes. **Requirements**: - Degree in CTF, Biotechnology, Pharmacy, Chemical Engineering, Management Engineering or similar.
- Ideally 6 months / 1 year of experience in similar roles in the pharmaceutical sector.
- Proficiency in English, both written and oral.
- Post degree courses in QA will be considered a plus. **Knowledge, Skills, Abilities**
- GMP knowledge
- Knowledge of main IT softwares
- Leadership
- Independence in handling tasks
- Ability to work in a team We offer an initial fixed term contract for 12 months. At our company, each one of our 70,000 outstanding minds has a unique story to tell. Join us and let's reach our mission—enabling our customers to make the world healthier, cleaner and safer!