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Validation Expert
Job summary
A global healthcare leader in Saluggia, Italy is searching for a Validation Expert responsible for managing validation activities and ensuring compliance with cGMP standards. The ideal candidate will have a scientific degree and experience in a sterile GMP environment, along with fluency in Italian and English. This role involves collaborating across teams to support validation processes and technical transfers. Join us in supporting patients globally.
Qualifications
- Scientific Degree (CTF/Pharmacy/Biotechnology/Chemical Engineering or related field).
- Previous experience in a similar role within a sterile GMP environment.
- Knowledge of Quality and IT tools.
- Fluent in Italian and English.
Responsibilities
- Support site validation planning by writing and maintaining master plans for processes, cleaning, packaging.
- Support process validation lifecycle activities by ensuring a state of control is maintained.
- Author and review validation protocols & reports.
- Support execution of validation activities at the shop floor.
- Review Master Batch Records and associated change controls.
- Provide technical expertise for pre-validation risk assessments.
- Ensure all site validation activities are compliant with requirements.
- Collaborate for technical transfers and new product launches.
- Facilitate establishment of Quality Risk Assessment.
The Validation Expert is responsible for executing and managing process, primary packaging and cleaning validation activities and change management activities to meet cGMP requirements on time and quality to ensure that site validation programs are compliant with global regulatory exceptions.
- Support site validation planning by writing and maintaining master plans for processes, cleaning, packaging.
- Support process validation lifecycle activities by ensuring a state of control is maintained through ongoing.
- Author and review process, packaging or cleaning validation protocols & reports, ongoing process and cleaning verification protocols & reports.
- Support execution of validation activities at the shop floor.
- Reviews Master Batch Records and associated change controls. Confirm revalidation need based on technical changes.
- Provides technical expertise (and may facilitate) pre-validation risk assessments using risk management tools.
- Work collaboratively and cross functionally to help ensure that process risks are analyzed, appropriately controlled and appropriately documented.
- Ensure that all Site validation activities are performed and are in line with the current Novartis requirements and cGMP, manage deviations associated with process validation and makes recommendations for deviation resolution as well as prevention of reoccurrence.
- Work in close collaboration with development organization (or sending site) for technical transfers and newproduct launches to ensure that knowledge is transferred, control strategies are appropriate, risks are analyzed and controlled and to ensure that commercial processes are validation ready.
- Provide technical expertise and facilitate establishment of Quality Risk Assessment (as needed).
- Scientific Degree (CTF/Pharmacy/Biotechnology/Chemical Engineering or related field).
- Previous experience in a similar role within a sterile GMP environment.
- Knowledge of Quality and IT tools.
- Fluent in Italian and English.
Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together?
https://www.novartis.com/about/strategy/people-and-culture
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* The salary benchmark is based on the target salaries of market leaders in their relevant sectors. It is intended to serve as a guide to help Premium Members assess open positions and to help in salary negotiations. The salary benchmark is not provided directly by the company, which could be significantly higher or lower.