Monza site is a world class contract manufacturing facility, specialized in aseptic injectable drugs. Joining more than 1000 colleagues on site, the selected candidate will experience a smart, driven, and fast growing environment. With revenues of more than $24 billion and the largest investment in R&D in the industry, we give our people the resources and opportunities to make significant contributions to the world.

You will join the Process & Cleaning Validation team, within the QA function, to support the team in ensuring the validation of FDA-approved sterile production processes and cleaning activities. You will be responsible for writing protocols, executing validation activities and writing validation reports, in compliance with cGMP, Clients’ needs and the Company's quality standards.
The Process & Cleaning Validation Specialist will be directly involved in Technology Transfer projects as a subject matter expert and will closely interact with our international clients.

This is entry-level temporary role is the ideal step for a young QA professional, who is willing to further consolidate his/her technical skills and take up increasing responsibilities in an international environment.

In this role you will gain an unmatched experience in technology transfers of sterile injectable products that will be invaluable for your next career step in Thermo Fisher Scientific.


Essential Functions

• Ensure the correct validation and cleaning project process, through the coordination and supervision of activities in compliance with protocols and procedures.
• Be responsible for the technical documentation analysis in order to obtain information that will help him/her to write protocols and validation reports and execute validation activities in compliance with company procedures, Clients’ needs and cGMP.
• Analyze generated data from validation activities and other internal functions, support the other internal function such as the Batch Record and Investigation Team during the handling of any deviations in accordance with protocols and business procedures.
• Manage deadlines, change control activities and corporate procedures related to the whole production process, systems, products.
• Ensure and work for the correct execution of external audits through the provision of necessary information and documentation.

• Knowledge of pharmaceutical processes validation and main analytical methods
• Knowledge of GMP, pharmaceutical legislation and national and international guidelines
• Fluent English (written and spoken)
• At least 1 years of previous experience in QA or QA Validation. in a  pharmaceutical manufacturing facility.

At Thermo Fisher Scientific, each one of our 70,000 extraordinary minds has a unique story to tell. Join us and contribute to our singular mission—enabling our customers to make the world healthier, cleaner and safer.