Verified Job
IT / Software / Data Analyst
Pharma Technical Regulatory Submission Intern
IT / Software / Data Analyst
#814449
Remote / WFH
Roche ·
Job Description
At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.
The Position
As a Pharma Technical Regulatory Submission Intern, you will join our global team in Mississauga to support the delivery of high-quality regulatory submissions to health authorities worldwide. You will work alongside cross-functional experts to manage critical submission processes and maintain global compliance for our life-saving portfolio. This 12-month internship offers an exciting opportunity to build core expertise in regulatory operations, project management, and data systems while contributing to meaningful patient outcomes.
The Opportunity:
• Prepare global (CMC) regulatory submissions, including Module 3 CTD dossiers and electronic formatting standards.
• Manage regulatory information systems and documentation across diverse health authority submission types.
The Position
As a Pharma Technical Regulatory Submission Intern, you will join our global team in Mississauga to support the delivery of high-quality regulatory submissions to health authorities worldwide. You will work alongside cross-functional experts to manage critical submission processes and maintain global compliance for our life-saving portfolio. This 12-month internship offers an exciting opportunity to build core expertise in regulatory operations, project management, and data systems while contributing to meaningful patient outcomes.
The Opportunity:
• Prepare global (CMC) regulatory submissions, including Module 3 CTD dossiers and electronic formatting standards.
• Manage regulatory information systems and documentation across diverse health authority submission types.
