HOW YOU WILL MAKE AN IMPACT

• The Director Scientific and Regulatory Affairs will advance the success of existing products through best-in-class research, scientific content, and clinical substantiation
• Anticipate and advise on future regulatory trends and direction and frequently recommend preemptive approaches for company regulatory compliance.
• Lead all regulatory matters, including labeling requirements, domestic and international filings, FDA and FTC document submissions, and manage third-party consultants
• Director Scientific and Regulatory Affairs will conduct timely and enhanced regulatory reviews to support commercialization of private label and custom product formulations
• Liaise and foster relationships with government agencies and trade organizations. Advise on emerging policies and legislative matters
• Director Scientific and Regulatory Affairs will assess market trends, relevant legislation, and consumer needs to ensure product compliance, relevance, and prominence
• Manage and direct research and development programs to meet organizational needs and to capitalize on GHW’s various brands
• Director Scientific and Regulatory Affairs will work closely with other departments (Legal, Quality, Procurement, and Distribution Center) to develop new product specifications that are compliant with the Code of Federal Regulations and compatible with GHW’s infrastructure

Please refer the Job description for details