Associate, Regulatory Affairs
Amgen View all jobs
- Mississauga, ON
- $73,205-99,043 per year
- Permanent
- Full-time
- Execute the preparation, delivery, and electronic archiving of documentation for inclusion in local Regulatory submissions.
- Partner with International Regulatory Leads (IRLs) and cross-functional team members to support the coordination and execution of local Regulatory submissions.
- Coordination and execution of Regulatory Affairs processes and deliverables to ensure submissions are made on time and meet Amgen’s corporate and local regulatory requirements.
- Disseminate and exchange relevant information to team(s) as appropriate.
- Contribute to and support implementation of filing plans, where applicable.
- Support local labelling activities, including the review of source text and translations for country labelling.
- Participate in local Regulatory process improvement initiatives.
- Under general supervision, interact with local Health and Regulatory authorities for routine matters.
- Ensure/support regulatory product compliance (e.g. Health Canada commitments).
- Partner with peers to ensure consistency in implementation of local policies and procedures.
- Knowledge of drug development
- Knowledge of regulations, guidelines and regulatory principles
- Knowledge of the registration procedures in Canada for clinical trial applications, marketing applications and post-approval changes
- Scientific / Technical excellence
- Adherence to policies, procedures, and standard operating procedures (SOPs)
- Effective communication
- Cross-functional collaboration and teamwork
- Flexibility and adaptability
- Demonstrates strong initiative and attention to detail
- Bachelor of Science degree
- Regulatory affairs experience
- 1+ year of Regulatory affairs experience
- Regulatory Affairs Graduate Certificate
- Ability to understand and communicate scientific/clinical information
- Ability to anticipate and prevent potential issues
- Understanding of Regulatory activities and their touch points