
Regulatory Affairs Professional
1 day ago
Regulatory Affairs Professional
The ideal candidate will be responsible for working closely with international regulatory teams to ensure compliance with Indian regulations.
- Develop and maintain in-depth knowledge of India's Medical Device Regulations (MDR).
- Collaborate with cross-functional teams to implement effective regulatory strategies.
- Identify and mitigate potential risks associated with regulatory non-compliance.
- Develop and maintain relationships with external stakeholders, including regulatory bodies and consultants.
- Provide guidance and support to colleagues on regulatory matters.
Key Qualifications
- Bachelor's degree in a relevant field, such as Regulatory Management or a related discipline.
- Minimum 1-3 years of experience in regulatory affairs, preferably in the medical device industry.
- Strong understanding of India's MDR and ability to apply this knowledge in a practical setting.
- Excellent communication and interpersonal skills, with the ability to work effectively with colleagues at all levels.
- Ability to prioritize multiple tasks and manage competing deadlines.
Benefits
- Opportunity to work with a leading organization in the medical device industry.
- Chance to develop and expand your skills and expertise in regulatory affairs.
- Collaborative and dynamic work environment.
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