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Roche fosters diversity, equity and inclusion, representing the communities we serve. When dealing with healthcare on a global scale, diversity is an essential ingredient to success. We believe that inclusion is key to understanding people’s varied healthcare needs. Together, we embrace individuality and share a passion for exceptional care. Join Roche, where every voice matters.
The Position
Embark on a transformative two-year journey with the One PDR ET Program, meticulously crafted to impart comprehensive foundational knowledge in regulatory affairs. This dynamic initiative blends hands-on assignments with tailored learning solutions, making it an ideal entry-point for aspiring regulatory professionals. Eligible candidates should possess a Bsc in life or pharmaceutical sciences, or an equivalent scientific qualification, and have less than one year of relevant pharmaceutical regulatory experience. Participants gain invaluable insights into the complete lifecycle of pharmaceutical products, from initial clinical trials to market exit, by engaging in diverse activities across various therapeutic areas and stages of development. The latter part of the program offers the opportunity to rotate into another Product Development function or specialize further in PDR.
Throughout the program, ETs collaborate with global drug development teams to support the introduction of novel pharmaceutical products to patients worldwide. This environment not only enhances their scientific writing skills but also deepens their understanding of regulatory frameworks by preparing a wide array of regulatory documents. By joining the One PDR ET Program, participants become pivotal contributors to the regulatory landscape, dedicated to ensuring that life-changing medicines reach those who need them most.
The opportunity:
- Delivers on projects with mentorship and actively builds foundational regulatory experience with the support of colleagues
- Owns their learning and development, actively seeking to understand drug development and regulatory roles, and engaging in knowledge sharing and peer support
- Responsible for understanding and applying business processes to deliver foundational regulatory deliverables
- Engages with the team through active listening, practicing open communication, and building trust within regulatory and cross-functional teams
- Grasps the vision of the Roche organization, understanding how their work impacts the team and contributes to overall goals
- Improves prioritization and time management skills while spending significant time on-site at Roche/Genentech offices
Who you are:
- You hold a minimum qualification of a first degree in a life sciences, biological sciences, biology, chemistry, Pharmacy, or related field before the start of the program, and you are within two years of completion of a degree program in the before mentioned disciplines.
- You have basic understanding of drug development and entry level understanding of the role of a regulatory professional
- Maximum 1 year relevant pharmaceutical experience post last degree
- Demonstrates a learning mentality, engages in personal growth, and actively seeks and acts on feedback
- Fosters partnership, collaboration, empowerment, and autonomy to build a strong community
Additional Information:
- Division: Pharma
- Department: Global Product Development Regulatory (PDR)
- Reports to: Functional/Senior Functional Manager
- Location: Hybrid, Based in Mississauga, ON
- Hours: full-time (35 hours per week)
- Length: This opportunity is a 2-year work term
The statements made in this job description are intended to describe the general nature and level of work being performed by those persons assigned to this job. These statements are not intended to be a comprehensive list of all responsibilities, duties and skills required of people assigned to this job.
This position is not eligible for relocation support.
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Who we are
At Roche, more than 100,000 people across 100 countries are pushing back the frontiers of healthcare. Working together, we’ve become one of the world’s leading research-focused healthcare groups. Our success is built on innovation, curiosity and diversity.
Roche Pharma Canada has its office in Mississauga, Ontario and employs over 850 employees. The Mississauga facility is bright, vibrant, fosters collaboration and teamwork, and is reflective of Roche’s truly innovative culture.
As of January 4, 2022, Roche requires all new employees who work in Canada to be fully vaccinated against COVID-19 on the date they take office. This requirement is a condition of employment at Roche that applies regardless of whether the position is on a Roche campus or remotely. If you have a valid reason for not being fully immunized, which is limited to certain specific medical reasons or other valid reasons protected by applicable human rights laws, you may request an exemption and / or adaptation measures regarding this vaccination requirement.
Roche is an Equal Opportunity Employer.
