Stilling
End of 2024, Novo Nordisk acquired the manufacturing site Catalent Anagni S.r.l. with the ambition to expand our capacity to meet the needs of millions of patients. You will be part of a global team that will develop the pharma facilities of the future and work with advanced technology to rethink our fill & finish facilities.
As a QA Validation Specialist, you'll play a critical role in
ensuring the integrity and compliance of our products from the very
beginning. If you are passionate about quality assurance in the
pharmaceutical industry, we want to hear from you!
Join Novo Nordisk, a global leader in diabetes care, and be a
pivotal part of our commitment to quality and innovation!
The Position
Your main responsibilities, will be:
• Conduct a comprehensive review of all equipment
qualification activities and process validation
• Monitor QA milestones, assist in issue resolution, and
interact effectively with internal and external stakeholders for
risk mitigation.
• Collaborate in the preparation and execution of
pre-approval inspections for approval of new departments and
customer audits for new product introductions.
• Review and manage all documentation related to Quality
Assurance activities, including Master Batch Records and procedures.
• Ensure compliance with GMP during batch releases and
support investigations of deviations as necessary.
Qualifications
As our ideal candidate, you have a bachelor’s degree in life
science and a minimum of 5 years of experience in quality assurance,
focusing on Quality Operations and Qualification/Validation
activities for sterile production (Vials and Pre-Filled Syringes).
In addition, you have:
• In-depth knowledge of regulatory requirements and
guidelines (e.g., FDA, EMA, ICH) related to Sterility Assurance and
Qualification/Validation activities.
• Strong understanding of pharmaceutical quality management systems.
• Experience in sterile manufacturing would be highly appreciated
• Diversified experience across different functional areas
and/or quality.
• Advanced and fluent English skills.
• Management and leadership skills aimed at enhancing
organizational synergies.
• Robust knowledge of manufacturing processes, products,
documentation, and procedures.
Working at Novo Nordisk
At Novo Nordisk, we don’t wait for change. We drive it. We’re a
dynamic company in an even more dynamic industry, and we know that
what got us to where we are today is not necessarily what will make
us successful in the future. We embrace the spirit of
experimentation, striving for excellence without fixating on
perfection. We never shy away from opportunities to develop, we
seize them. From research and development, through to manufacturing,
marketing and sales – we’re all working to move the needle on
patient care.
Contact
If you believe you are qualified, and cannot wait to take the
challenge, please upload your CV directly via our online application
tool.
Deadline
Apply before June 9th, 2025 .
We commit to an inclusive recruitment process and equality of opportunity for all our job applicants.
At Novo Nordisk we recognize that it is no longer good enough to aspire to be the best company in the world. We need to aspire to be the best company for the world and we know that this is only possible with talented employees with diverse perspectives, backgrounds and cultures. We are therefore committed to creating an inclusive culture that celebrates the diversity of our employees, the patients we serve and communities we operate in. Together, we’re life changing.