Job Description When you're part of Thermo Fisher Scientific, you'll do challenging work, and join a team that values performance, quality and innovation.
As part of a successful, growing global organization you will be encouraged to perform at your best.
With revenues of more than $40 billion and the largest investment in RD in the industry, we give our people the resources and chances to create significant contributions to the world.
In Monza we offer compliance with controlled drug regulations in Europe and the U.S. as well as disposable manufacturing technologies and fully integrated secondary packaging services, and has received regulatory approval from various international regulatory inspection agencies, including: ANVISA, JP PMDA, US FDA, EMA, GCC States, Canada, Russia, Taiwan, Turkey.
The Monza site currently supplies over 20 countries – all the major international markets, including the U.S., Europe and Asia Pacific!
You will join the PDS Analytical Development GMP Department in a newly built Pharmaceutical Department (PDS).
Reporting to the PDS AD GMP Supervisor, you are responsible for the assigned projects and all related documentation (OOS/OOT/Change control, SOPs and CoA) to ensure the successful continuation of the projects within the PDS.
What you will do Responsible for the analytical documentation of APIs, Excipients and DP (release and stability tests).
Collaborate with Clients, QC PDS, Regulatory Department, QC Compliance, QA, and QO to issue the correct documents for PDS projects, respecting the ICH and Pharmacopoeia.
Provide compliance consulting and strategic advice to internal and external clients to determine the most appropriate approach to compliant documentation for their products.
Provide project-specific strategy, technical expertise in QC Documentation matters, and coordination oversight for key clients' projects.
Serve as the executive contact for key clients for all issues, including attendance at regulatory authority meetings and other public relation functions.
Ensure quality performance for key/managed projects.
Responsible for the evaluation of OOS, OOT, and laboratory investigations in terms of recurrences, root cause, trend, and defining CAPAs.
Perform laboratory investigations, laboratory OOS and OOT, and any deviations and CAPA related to them, collaborating with Supervisor and Team Leader to manage these.
How will you get there Bachelor's degree in chemical engineering, chemistry, or equivalent work experience with pharmaceutical companies.
GMP standards applied to Quality Control laboratories, with particular reference to stability studies, laboratory data management, and SOP writing.
Proficiency in English and Italian.
Flexibility and adaptability.
Good organization and planning skills.
Excellent listening, oral, and written communication skills.
Ability to work in a team.
At Thermo Fisher Scientific, each one of our 100,000 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.
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