Manager, Regulatory Affairs

3 weeks ago

Toronto, Canada Johnson & Johnson Full time

Johnson & Johnson Innovative Medicine is recruiting for a Manager, Regulatory Affairs to be located in Toronto, Ontario under the flexible working model (at least 3 days in office).

For more than 130 years, diversity, equity & inclusion (DEI) has been a part of our cultural fabric at Johnson & Johnson and woven into how we do business every day. Rooted in Our Credo, the values of DEI fuel our pursuit to create a healthier, more equitable world. Our diverse workforce and culture of belonging accelerate innovation to solve the world’s most pressing healthcare challenges.

We know that the success of our business - and our ability to deliver meaningful solutions - depends on how well we understand and meet the diverse needs of the communities we serve. Which is why we foster a culture of inclusion and belonging where all perspectives, abilities and experiences are valued and our people can reach their potential.

At Johnson & Johnson, we all belong.

Key Responsibilities:

- Develop and implement regulatory strategic plans for product registration and lifecycle management.
- Lead the preparation of regulatory submissions including New Drug Submissions (NDSs), Supplemental New Drug Submissions (SNDSs), and ad hoc reports to Health Canada, and maintain the life cycle of currently marketed products. The focus of this role is on the clinical/therapeutic claims and not the Chemistry, Manufacturing and Controls.
- Lead interactions with Health Canada throughout the submission review cycle to ensure timely regulatory approval and optimal labelling.
- Collaborate with global cross-functional teams and the Global Regulatory Affairs (GRA) function/teams to facilitate regulatory activities.
- Collaborate with internal partners to ensure alignment of regulatory affairs strategy with business priorities, and to meet strategic business objectives and stretch goals.
- Develop effective working relationships with business partners and the authorities to support regulatory strategies.
- Manage emerging issues (e.g. new safety finding) and the associated risk communications.
- Provide regulatory guidance and input to internal partners on messaging, promotional material review, and PAAB responses.
- Monitor the regulatory environment, interpret changes, analyze gaps and conduct impact assessment, and participate/lead implementation into systems/processes.
- Actively contribute to the improvement of departmental processes and initiatives to enhance the internal work environment.
- Mentor and develop interns and/or direct reports as applicable.

**Qualifications**:
**Education**:

- A minimum B.Sc. in Biological or related sciences. MSc/PhD preferred.

Experience and Skills:
Required:

- Minimum 5 years of pharmaceutical or medical device Regulatory Affairs or related experience.
- Experience with the preparation and approval of regulatory submissions for brand name prescription drugs to a major Regulatory Authority (e.g. Health Canada, FDA, EMA, MHRA, TGA, SwissMedic).
- Strong working knowledge of the drug development process.
- Knowledge of Canadian drug laws, regulations, guidelines and policies, and the Health Authority organizational structure and processes for the review and approval of drug submissions.
- Ability to interpret and understand Regulations in the context of the scientific and commercial environment.
- Strong scientific writing skills.
- Ability to interpret and summarize clinical data.
- Strong problem solving and analytical skills.

Preferred:

- Ability to interpret basic biostatistics and observational research methodologies.

Diversity and inclusion are central elements of the shared culture across the Johnson & Johnson Family of Companies. Attracting, developing and retaining a workforce that reflects the diversity of our customers and communities is essential to our success. We are committed to providing a respectful, inclusive and accessible work environment where all employees have the opportunity to achieve their potential.

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