Validation Expert

Jobs for Humanity; Ivrea; In loco; EUR 40.000 - 60.000; Tempo pieno

Descrizione del lavoro

A healthcare organization is seeking a Validation Expert in Ivrea, Italy. This full-time role involves managing process validation activities and ensuring compliance with cGMP requirements. The ideal candidate will hold a scientific degree and have prior experience in a sterile GMP environment, alongside fluency in Italian and English. Key responsibilities include supporting validation planning, executing validations, and collaborating technically with various departments. Skills in Python, debugging, and technical writing are essential.

Competenze

• Experience in a similar role within a sterile GMP environment.
• Fluent in Italian and English.
• Knowledge of Quality and IT tools.

Mansioni

• Execute and manage process validation activities to meet cGMP requirements.
• Support site validation planning and maintain master plans.
• Review process validation protocols and reports.

Conoscenze

Python

Debugging

Technical Writing

cGMP

FDA Regulations

Minitab

SOC

GAMP

OS Kernels

C / C++

Manufacturing

Formazione

Scientific Degree (CTF / Pharmacy / Biotechnology / Chemical Engineering)

Descrizione del lavoro

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.

About the Role

Major accountabilities :

• 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).

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.

Why Novartis

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 our Novartis Network : Not the right Novartis role for you Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up : and Rewards : Read our handbook to learn about all the ways well help you thrive personally and professionally : Work :

Employment Type

Full-time

Key Skills

• Python
• SOC
• Debugging
• C / C++
• FDA Regulations
• Minitab
• Technical Writing
• GAMP
• OS Kernels
• Perl
• cGMP
• Manufacturing

Experience

years

Vacancy

1