Generic Drug Specialist

6 days ago


Oakville, Ontario, Canada SteriMax Inc. Full time

SteriMax Inc. is seeking a highly motivated and detail-oriented Regulatory Affairs Associate to join our team.

Job Summary

The Regulatory Affairs Associate will play a key role in ensuring the success of our generic drug products through regulatory submissions and compliance.

Main Responsibilities:

  • Prepares regulatory submissions for generic drug products.
  • Manages submissions under regulatory agency review.
  • Collaborates with internal teams to ensure compliance and quality control.
  • Maintains accurate records and reports.

Key Requirements:

  • University degree in a related field.
  • Minimum 3 years of experience in regulatory affairs.
  • Strong analytical and problem-solving skills.
  • Excellent communication and teamwork skills.


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