Regulatory Affairs Director, Pharmaceuticals – Northeast (1736)
Our client, a leader of innovation in the pharmaceutical industry, is seeking a Regulatory Affairs Director to join their team. This person would be responsible for ultimate accountability for regulatory compliance and product stewardship.
Requirements:
- Fifteen+ years leading teams in pharmaceutical manufacturing regulatory work– APIs, excipients, contract manufacturing, etc.
- Master’s Degree in Pharmaceutical Science,or other related field.
- Solid understanding of quality issues and how they relate to regulatory.
- Willing to travel internationally to manage the global teams.
- Must be proactive and stay ahead of regulatory changes/requirements.
- Must be confident and collaborative.
Location/Travel: Hybrid role (split between home office and onsite) based in DE. Up to 25% travel per year.
Why Consider This Job/Company?
- This person will be leading a very collaborative, close knit team of seasoned professionals.
- The hiring manager is warm, personable, and reasonable. They place a high value on collaboration.
- This is a key position for the company as this person will set the overarching global regulatory strategy for this business unit.
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