Regulatory Compliance Specialist
2 weeks ago
Regulatory Affairs Specialist
Company: GForce Life Sciences
Employment Type: Full-time, 12-month contract
Overview: GForce Life Sciences is seeking a dedicated regulatory affairs specialist. This role involves crafting and executing regulatory strategies in partnership with diverse stakeholders within the medical device sector.
Primary Responsibilities:
- Develop and implement regulatory strategies
- Effectively communicate regulatory issues to management and stakeholders
- Maintain strong visibility with both internal and external partners
- Exhibit excellent communication skills
- Collaborate with internal teams to fulfill regulatory requirements
- Oversee and monitor strategic projects
- Ensure the timely execution of regulatory strategies and activities
- Convey regulatory requirements to project teams
Required Qualifications:
- Bachelor's degree in engineering or a scientific discipline; a master's degree is preferred
- A minimum of 3 years of experience in regulatory affairs
- Familiarity with US and/or Canadian regulatory frameworks
- Experience in preparing regulatory submissions
- Strong negotiation, influence, and conflict management skills
- Prior experience in the medical device, food, or pharmaceutical sectors is advantageous
- Proven ability to write clearly and effectively
Contract Terms:
- 12-month contract with potential for extension
- Full-time position, 40 hours per week
- Onsite role
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