Regulatory Affairs Expert for Global Pharmaceutical Development
1 giorno fa
Pfizer, S.A. de C.V seeks a skilled Regulatory Affairs Expert to support the development and approval of innovative medicines.
The ideal candidate will possess in-depth knowledge of global regulatory environments, with a focus on EU regulations. Key responsibilities include providing strategic regulatory guidance, leading/co-leading projects, managing own time to achieve objectives, and ensuring business compliance with regulatory standards.
Required Skills and Qualifications:
Bachelor's Degree and 5+ years of experience in the Over-the-Counter or pharmaceutical industry. A strong background in commercial activities, Current Good Manufacturing Practices (part of GxP), and ability to work cross-functionally are essential. Relevant pharmaceutical experience and audit process management skills are a plus.
Benefits:
Pfizer offers competitive compensation and benefits packages, including salary range $140,000 - $180,000 per year, based on location and experience.
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