Quality Assurance Systems Internship - Garbagnate Milanese, Italia - Bayer

Bayer

Azienda verificata

Garbagnate Milanese, Italia

3 settimane fa

Inviato da:

Piero Bianchi

Reclutatore di talenti per beBee

StageSHIP

Descrizione

At Bayer we're visionaries, driven to solve the world's toughest challenges and striving for a world where ,Health for all, Hunger for none' is no longer a dream, but a real possibility. We're doing it with energy, curiosity and sheer dedication, always learning from unique perspectives of those around us, expanding our thinking, growing our capabilities and redefining 'impossible'. There are so many reasons to join us. If you're hungry to build a varied and meaningful career in a community of brilliant and diverse minds to make a real difference, there's only one choice.

Quality Assurance Systems Internship (M/F)

Bayer Healthcare Manufacturing is looking for two brilliant new graduates to be insert in the Quality Department of Garbagnate plant.

You will be involved in supporting the "Nitrosamine Project and Regulatory compliance activities" or in "Implementation of a new GMP documentation system management and QA Systems activities".

YOUR MAIN RESPONSIBILITIES:

Nitrosamine Project and Regulatory compliance activities:

Support for regulatory compliance topics, with focus on the implementation of Nitrosamine EMA/425645/2020 regulatory requirement
Consolidate Internal Technical Registration document according to Risk evaluation and to follow Confirmatory Testing and mitigation actions step
Collaborate in cross functional environment, with Local and Divisional experts
Support the team in processing requests for regulatory variations, collaborating with Global Regulatory Affair function.

Implementation of the new GMP documentation system management and QA systems activities:

Support the team in the implementation of the new electronic system used for the review and approval of GMP document
Support in the creation of new SOPs for GMP documentation management according to the new process
Collaborate in cross functional environment, with Local and Divisional experts
Support in the management of Site GMP training records
Oversight of Site GMP documentation and QA systems KPIs

WHO YOU ARE:

Master's degree in CTF or Pharmacy
Excellent knowledge of the Microsoft Office Package
Excellent digital skills
Strong ability of organization and coordination (lean methodology)
The natural predisposition to teamwork, spirit of initiative, precision and sense of responsibility complete the soughtafter profile
Fluent knowledge of English and Italian are mandatory