Validation Expert

Novartis Italia; Ivrea; In loco; EUR 35.000 - 45.000; Tempo pieno

Descrizione del lavoro

A leading pharmaceutical company located in Piemonte, Italy is seeking a Validation Expert responsible for managing validation activities to ensure compliance with global regulatory requirements. The ideal candidate should have a scientific degree and experience in a sterile GMP environment, along with fluency in Italian and English. This is an entry-level full-time position with opportunities for professional growth.

Competenze

• Previous experience in a similar role within a sterile GMP environment.

Mansioni

• Support site validation planning by writing and maintaining master plans for processes, cleaning, packaging.
• Author and review validation protocols & reports, ongoing process and cleaning verification.
• Work collaboratively to analyze and document process risks.

Conoscenze

Knowledge of Quality and IT tools

Fluent in Italian

Fluent in English

Formazione

Scientific Degree (CTF/Pharmacy/Biotechnology/Chemical Engineering or related field)

Descrizione del lavoro

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.

About The Role

• 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 make 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).

Essential Requirements

• 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.

Benefits and Rewards

Read our handbook to learn about all the ways we’ll help you thrive personally and professionally: https://www.novartis.com/careers/benefits-rewards

Seniority level

Entry level

Employment type

Full-time

Job function

Quality Assurance

Industries

Pharmaceutical Manufacturing