Attiva gli avvisi di lavoro via e-mail!
Aumenta le tue possibilità di ottenere un colloquio
Crea un curriculum personalizzato per un lavoro specifico per avere più probabilità di riuscita.
Join a leading consulting firm as a Quality Assurance Validation Specialist in the Pharmaceutical industry. You'll manage validation activities, ensuring compliance with cGMP requirements in a supportive environment. Enjoy travel reimbursements and access to wellness programs as part of your career development.
Would you like to start a new professional adventure as a Quality Assurance Validation Specialist in the Pharmaceutical industry in Rome?
You will be part of a Top Employer certified company supporting its partners in key areas for Pharma and Biomed Industries, including Quality, Laboratories, R&D, and Production.
The Validation Specialist is responsible for executing and managing equipment, facility, utility, process, and primary packaging validation activities, as well as change management activities, to meet cGMP requirements. The goal is to ensure that site validation programs are compliant with global regulatory expectations, delivered on time and with quality.
Amaris Consulting is an independent technology consulting firm providing guidance and solutions to businesses. With over 1000 clients worldwide, we have been implementing major projects for over a decade. Our international team of 6000 professionals spans across 5 continents and more than 60 countries. Our solutions focus on four Business Lines: Information System & Digital, Telecom, Life Sciences, and Engineering. We are committed to building and nurturing a top talent community where everyone can reach their full potential. Amaris is your stepping stone to navigate change, meet challenges, and successfully achieve your projects.
We look forward to meeting you!
Position: Quality Assurance Specialist
Location: Aprilia, Italy