Regulatory Affairs Professional

1 day ago


Bengaluru, Karnataka, India beBeeRegulatory Full time

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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