Compliance Coordinator
November 12
Description
• Establish supplier evaluations and re-evaluations as per company procedures. • Assisting with regulatory compliance activities, including documentation review and maintenance. • Supporting the preparation and submission of regulatory documents, such as design dossiers and technical files. • Assisting with quality management system activities, including preparing for audits. • Collaborating with cross-functional teams to ensure compliance with regulatory requirements. • Staying updated on relevant regulations and industry standards.
Requirements
• Bachelor's or Master’s degree in engineering, law, or a related field. • Strong organizational and time management skills. • Attention to detail. • Good communication and interpersonal skills. • Proficiency in English, both written and spoken. • A keen interest in medical devices and a willingness to learn. • No work experience in the regulatory field is required. • Available for full time role.
Benefits
• A challenging and rewarding role in a growing company. • An introduction to regulatory and compliance work for medical device software. • The opportunity to work with experienced professionals in the medical device industry. • A supportive and collaborative work environment in a small team • Work in the office or at home, it’s 100% your choice. • Competitive salary and benefits package. • Pending team needs, your maternity cover employment may be extended to a regular full time role.
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