Regulatory Officer
at Canadian Nuclear Laboratories
Chalk River, ON, Canada -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 27 Dec, 2024 | Not Specified | 28 Sep, 2024 | N/A | Good communication skills | No | No |
Required Visa Status:
Citizen | GC |
US Citizen | Student Visa |
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OPT | H4 Spouse of H1B |
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Employment Type:
Full Time | Part Time |
Permanent | Independent - 1099 |
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Contract to Hire – Corp 2 Corp |
Description:
Can you see yourself supporting the Manager of Regulatory Affairs to coordinate licensing activities within CNL with particular emphasis on CRL, prepare licensing documents, coordinating preparations for CNSC hearings and meetings, and providing recommendations for licensing strategies based on knowledge of the regulations and project or program requirements? Are you looking for a role that will challenge you? If you answered yes, then this may be the job for you!
Responsibilities:
- Preparing and reviewing licensing correspondence
- Assisting the Manager, Regulatory Affairs with the oversight of all licensed activities conducted by CNL and acting as a designate as required
- Participating as licensing representative in various meetings
- Reviewing and providing comments on CNSC issued regulatory documents in conjunction with Industry peers (OPG, BP, NB Power, COG) and submitting comments to CNSC staff
- Producing and reviewing correspondence, preliminary verbal and full unplanned event reports to the CNSC
- Providing input to strategic decisions and support strategic initiatives by reviewing and summarizing CNL, CNSC and other requirements and proposing optimal solutions to minimize licensing risk, while meeting project/program constraints
- Drafting and reviewing presentations for the CNSC, licensing procedures and processes, and responses to CNSC questions.
- Preparing licensing protocols, progress reports and other licensing submissions as required
- Managing routine communications with other CNL licensing areas
- Maintaining a schedule of all licensing activities for CRL and CNL
- Assisting in the preparation of the annual report by coordinating the production of CNL-CRL’s Annual Compliance Monitoring Reports (ACMR) and contributing as an author
- Tracking and managing regulatory commitments for CRL and CNL
- Providing regulatory assistance and guidance to CNL, especially, to the Designated Representatives of the Licensee (DROLs), i.e.,
- Program Authorities, Facility Authorities, and Safety and Control Area owners. Providing awareness training to CNL personnel on the branch documentation
- Assisting facilities and programs in compliance reviews to ensure they are meeting the requirements in the site license. May require coordination of various staff at CNL to achieve goals
- Producing and revising regulatory affairs process documentation and coordinating the production of this documentation
- Participating facilities and programs in the preparations for inspection and participating in inspections from a regulatory affairs perspective.
- Other duties as assigned by your manager.
REQUIREMENT SUMMARY
Min:N/AMax:5.0 year(s)
Pharmaceuticals
Pharma / Biotech / Healthcare / Medical / R&D
Clinical Pharmacy
Graduate
Proficient
1
Chalk River, ON, Canada