Regulatory Affairs Specialist
Full-time
Dempsey Resource Management Inc.
- Prepare and submit regulatory documents to health authorities.
- Monitor and analyze changes to regulations relevant to the company’s products.
- Develop and maintain regulatory strategies for new and existing products.
- Collaborate with cross-functional teams to ensure compliance and timely submissions.
- Provide guidance on regulatory requirements throughout the product lifecycle.
- Shall provide technical support to legal and registration activities of the RA Department in compliance to the regulatory requirements as mandated by specific regulatory agencies.
- Experience Level: 1–2 years in regulatory affairs or related field.
- Skills and Competencies: Strong analytical skills and attention to detail.
- Qualities and Traits: Excellent communication and interpersonal skills.
- Responsibilities and Duties: Ability to work under pressure and manage deadlines effectively.
Willing to do field work
preferably with experience on FDA registration preferably both medical device and pharma
Vacancy posted 15 hours ago
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