Process & Cleaning Validation Specialist Ii Lazio

Process & Cleaning Validation Specialist Ii
Roma
Lazio, Lazio

Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description About Thermo Fisher Scientific Inc. Thermo Fisher Scientific Inc. is a global leader in serving science, with a mission to enable our customers to make the world healthier, cleaner, and safer.

As one team of 100, 000+ colleagues, we are committed to accelerating research, solving complex scientific challenges, driving technological innovation, and supporting patients in need.

We value diverse experiences, backgrounds, and perspectives, and foster a collaborative and inclusive work environment.

Process Cleaning Validation Specialist II As a Process Cleaning Validation Specialist II at Thermo Fisher Scientific, you will have the opportunity to be part of a world-class team and contribute to the flawless validation of manufacturing processes and cleaning procedures.

Your expertise and proven experience will play a crucial role in ensuring the production of high-quality pharmaceutical products that meet strict regulatory requirements.

Responsibilities: Evaluate manufacturing process documents and equipment cleaning procedures for validation purposes Develop protocols and conduct process validation for product manufacturing and aseptic filling (Media fill) Perform cleaning validation of cleaning procedures and ensure periodic cleaning verification Manage validation protocols for cleaning, process, and Media Fill Collaborate with other departments to define protocol contents and actions to be carried out Validate manufacturing processes, cleaning procedures, and APS/Media Fill Support the drafting and approval of documents for new product transfer and validation Handle deviations related to validation activities Ensure accurate execution of validation activities and detailed analysis of results Draft validation reports and ensure proper archiving of all documentation Provide quality support for new product transfer and process qualification Actively participate in the design, construction, and implementation of new processes or manufacturing departments Requirements: Bachelor's Degree or equivalent in a scientific/pharmaceutical area 2 years of previous related experience in the pharmaceutical sector Knowledge of pharmaceutical techniques, production, and aseptic filling processes Experience in risk management and client service/project management Proficiency in Microsoft Office software Fluent in English with advanced written and oral communication skills #J-18808-Ljbffr