APR & CPV Specialist

3 settimane fa


Monza, Lombardia, Italia Thermo Fisher Scientific A tempo pieno

As a key member of our team, you will be responsible for ensuring the quality and compliance of our pharmaceutical products. Your primary focus will be on collecting and analyzing data to draft Annual Product Review Reports, as well as conducting periodic reviews of utilities and risk assessments for Continued Process Verification.

Key responsibilities include:

  • Collecting and analyzing data to draft Annual Product Review Reports
  • Conducting periodic reviews of utilities and risk assessments for Continued Process Verification
  • Ensuring the accuracy and completion of reports

Requirements for success in this role include:

  • Experience in data analysis and report writing in the pharmaceutical industry
  • Strong attention to detail and ability to identify trends and patterns in complex data sets
  • Knowledge of regulatory guidelines and standards (GMP, FDA, EMA, etc.)
  • Proficiency in statistical tools and software
  • Excellent communication and collaboration skills

At Thermo Fisher Scientific, we are committed to empowering our customers to improve global health, environmental cleanliness, and safety. We offer a collaborative and inclusive work environment where your expertise will be valued, and your contributions will have a direct impact on our success.



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