Roche is a global leader in pharmaceuticals and diagnostics, dedicated to advancing personalized healthcare and improving patient outcomes through innovative treatments and sustainable practices.
Switzerland 🇨🇭
Roche is a global pioneer in pharmaceuticals and diagnostics focused on advancing science to improve people’s lives. The combined strengths of pharmaceuticals and diagnostics under one roof have made Roche the leader in personalised healthcare – a strategy that aims to fit the right treatment to each patient in the best way possible. Roche is the world’s largest biotech company, with truly differentiated medicines in oncology, immunology, infectious diseases, ophthalmology and diseases of the central nervous system. Roche is also the world leader in in vitro diagnostics and tissue-based cancer diagnostics, and a frontrunner in diabetes management. Founded in 1896, Roche continues to search for better ways to prevent, diagnose and treat diseases and make a sustainable contribution to society. The company also aims to improve patient access to medical innovations by working with all relevant stakeholders. Thirty medicines developed by Roche are included in the World Health Organization Model Lists of Essential Medicines, among them life-saving antibiotics, antimalarials and cancer medicines. Roche has been recognised as the Group Leader in sustainability within the Pharmaceuticals, Biotechnology & Life Sciences Industry ten years in a row by the Dow Jones Sustainability Indices (DJSI). For more information, please visit https://careers.roche.com Read our community guidelines here: https://www.roche.com/some-guidelines.htm #Roche #Biotechnology #Pharmaceuticals #Diagnostics #Healthcare #PersonalisedHealthcare #GreatPlaceToWork #Innovation
Hybrid · Mississauga
Supports the preparation of regulatory submissions to Health Canada and participates in cross-functional meetings with global stakeholders. Responsible for maintaining regulatory compliance, updating SOPs, and managing electronic document systems.
Hybrid · Mississauga
The intern will support the Regulatory Affairs team in preparing and submitting various regulatory filings to Health Canada, including clinical trial and drug submission applications. They will also participate in cross-functional meetings and contribute to the maintenance of internal regulatory documentation and standard operating procedures.
Hybrid · Mississauga
The intern will support the preparation and global filing of CMC regulatory documents to ensure compliance and patient access to medicines. Key duties include coordinating cross-functional deliverables, monitoring project milestones, and supporting quality system maintenance.
Hybrid · Mississauga
The intern will support the preparation and global filing of CMC regulatory documents to ensure compliance and timely patient access to medicines. They will also coordinate cross-functional deliverables and monitor project milestones to uphold global manufacturing quality standards.