Regulatory Affairs Specialist

hace 5 días


San José, San José, Costa Rica Pfizer A tiempo completo

Key Activities:

The successful candidate will contribute to the completion of moderately complex projects, leveraging their regulatory knowledge to produce high-quality labeling materials.

They will utilize their expertise to ensure that all labeling-related documentation is accurate, compliant, and meets the required standards.

In addition, they will provide QC support to other labeling colleagues, identify areas for improvement, and develop solutions to enhance labeling-related processes and systems.

Essential Skills and Qualifications:

  • Regulatory affairs experience, preferably within pharmaceutical industry.
  • Excellent communication and interpersonal skills.
  • Ability to work independently and as part of a team.
  • Strong problem-solving and analytical skills.
  • Proficiency in Microsoft Office and other relevant software applications.
  • Familiarity with regulatory requirements and guidelines, including those related to labeling and product development.


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