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Validation Expert
Descrizione del lavoro
A leading global pharmaceutical company in Italy is seeking a Validation Expert to manage primary packaging and cleaning validation activities to ensure compliance with regulatory requirements. The ideal candidate will have a scientific degree, experience in a sterile GMP environment, and be fluent in Italian and English. Key responsibilities include supporting validation activities, risk assessments, and collaboration for technical transfers. This is a full-time position offering a dynamic work environment.
Competenze
- Previous experience in a similar role within a sterile GMP environment.
- Fluent in Italian and English.
- Knowledge of Quality and IT tools.
Mansioni
- Manage process primary packaging and cleaning validation activities.
- Review Master Batch Records and associated change controls.
- Support execution of validation activities at the shop floor.
Conoscenze
Formazione
Strumenti
Job Description Summary
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 new product 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.
- Assembly Language
- Change Control
- Chemical Engineering
- Chemistry
- Continual Improvement
- Process Cost Reduction
- Data Analytics
- Electronic Components
- General HSE Knowledge
- Including Gdp Knowledge
- Of Capa Knowledge
- Of GMP Lean Manufacturing Manufacturing Process Manufacturing Production Pharmaceutics Process and Cleaning Validation Process Control Process Engineering Risk Management Root Cause Analysis (RCA) Scheduler Six Sigma Sop (Standard Operating Procedure)
- Python
- SOC
- Debugging
- C / C++
- FDA Regulations
- Minitab
- Technical Writing
- GAMP
- OS Kernels
- Perl
- cGMP
- Manufacturing
Full-Time
years
1
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