What are the responsibilities and job description for the Head of Regulatory Affairs position at Meet Life Sciences?
About This Opportunity
We are seeking a highly skilled professional to lead our GMP/GLP quality functions, ensuring compliance with global regulatory requirements for manufacturing, preclinical, and testing operations. The ideal candidate will have a strong background in small molecule manufacturing and solid oral dosage forms.
Your Key Responsibilities:
- Develop and Implement Strategies: Develop and implement strategies to ensure compliance with global regulatory requirements for GMP/GLP quality functions.
- Lead and Mentor Teams: Manage and mentor a high-performing team, providing support, guidance, and professional development opportunities.
- Regulatory Expertise: Serve as the technical subject matter expert for GMP/GLP regulations, overseeing implementation of quality systems and processes.
- Cross-Functional Collaboration: Collaborate with cross-functional teams to integrate quality processes, support CMC and IND document review, and ensure continuous improvement in quality standards.
What We Offer:
- Competitive Compensation: A competitive salary and benefits package.
- Opportunities for Growth: Opportunities for professional growth and development.
- Diverse and Inclusive Environment: A diverse and inclusive work environment.
