ph3Process Cleaning Validation Specialit I /h3pIn this role you plan, execute, and document validation across equipment, processes, and computer systems to ensure product quality and regulatory compliance.
You will collaborate with cross-functional teams to uphold high standards and support continuous improvement.
The position offers growth within Thermo Fisher Scientific, a global leader in serving science.
You will tackle validation challenges with a focus on regulatory alignment, data integrity, and quality assurance.
This is a meaningful opportunity to contribute to critical healthcare and environmental safety initiatives.
/pulliPlan, execute, and document IQ/OQ/PQ validation activities for equipment, processes,



and computer systems /liliSupport regulatory compliance with FDA/EMA requirements and data integrity standards /liliCollaborate with cross-functional teams to maintain quality and drive continuous improvement /liliPerform risk assessments and ensure proper validation documentation and traceability /liliManage multiple validation activities and prioritise accordingly /liliTravel between sites may be required /liliBachelor's degree in a related field /liliStrong knowledge of validation principles (IQ/OQ/PQ) /liliExperience with equipment qualification and process validation /liliFamiliarity with FDA/EMA regulatory requirements /liliProficient in statistical analysis (Minitab) /liliStrong documentation and communication skills /liliExperience with risk assessment methodologies /liliKnowledge of data integrity and 21 CFR Part 11 compliance /liliAbility to work independently and in cross-functional teams /liliTravel flexibility for validation activities /li /ulpIn this role you plan, execute, and document validation across equipment, processes, and computer systems to ensure product quality and regu... /p /p #J-*****-Ljbffr

📌 Process & Cleaning Validation Specialit I (Lazio)
🏢 Experteer Italy
📍 Lazio