Quality Assurance Systems Internship (m/f)

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 join the Quality Department of Garbagnate plant.

He/she will be involved in supporting the “Regulatory compliance activities and implementation of a new electronic system for registration document management” or in “GMP Documentation &Training QA systems activities and project to improve electronic classification of GMP documentation archiving”.

YOUR TASKS AND RESPONSIBILITIES:

Regulatory compliance activities and implementation of a new electronic system for registration document management:

• Support the team in the implementation of the new electronic registration document management system
• Support the creation of new SOPs for registration document management according to the new process
• Support the team in processing requests for regulatory variations, collaborating with Global Regulatory Affair and Change Management functions
• Support the team in the monitoring of the approval status of regulatory variations
• Collaborate in cross functional environment, with Local and Divisional experts

GMP Documentation &Training QA systems activities and project to improve electronic classification of GMP documentation archiving:

• Support the team in organizing electronic classification of GMP documentation archiving
• Support the team in monitoring the correct document features and classification
• Collaborate with Local Experts in a cross functional environment
• Support in the management of Site GMP training records
• Support in the management of GMP annual training program
• Support in the 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 (lean methodology)
• The natural predisposition to teamwork, spirit of initiative, precision and sense of responsibility complete the sought-after profile
• Fluent knowledge of English and Italian mother tongue

Location: Garbagnate Milanese
Type of contract: Internship of 6 months