Regulatory Affairs Manager (Medical Devices)
- Coordinate and manage regulatory submissions and approvals in line with industry standards.
- Ensure compliance with applicable regulations and guidelines within the life sciences industry.
- Monitor regulatory changes and update internal processes as required.
- Provide strategic advice on regulatory matters to support business objectives.
- Develop and maintain relationships with regulatory authorities and key stakeholders.
- Prepare and review documentation to ensure accuracy and compliance.
- Collaborate with internal teams to align regulatory strategies with organisational goals.
- Support audits and inspections related to regulatory compliance.
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