Director of Regulatory Affairs - (US-NY-Rochester - 14694)

Minimum Education: Masters
Job Type: Full Time
Jobcode: 16063
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eConsultAmerica is a preferred vendor supplier on retainer with a global manufacturer who develops and markets cleaning, sanitizing, and maintenance products and services for the hospitality, institutional, and industrial markets. Our client is seeking an experienced and savvy Director of Regulatory Affairs. This position will be based in Minneapolis, MN. If you are interested please forward a brief cover-letter and your updated resume and I will respond back within one (1) business day. US Citizens or Green Card holders only apply.


Contact Information
eConsultAmerica
resumes@eConsultAmerica.com - Email
eConsultAmerica – Yahoo Instant Messenger
eConsultAmerica@skype.com – Skype Instant Messenger


POSITION DETAILS
The Director, Regulatory Affairs – Strategic Projects is responsible for developing regulatory strategy and providing project management leadership on key projects to support our client’s innovation in early stage product development (ideation/Phase 0/1). This newly created position will be global in scope and will support global product development projects, with emphasis on antimicrobial and handcare products. This leader will report directly to the Global Regulatory Affairs Vice President and will partner with Regulatory Affairs - Product Registration & Compliance and R&D product development teams to develop regulatory strategies that accelerate innovation in product development and commercialization. Working with external governmental agencies and academic thought leaders, the Director will influence outcomes of key product development and product registration projects.


BEST INDUSTRY – Manufacturing
BEST DEPARTMENT – Regulatory Affairs


QUALIFICATIONS
Bachelor’s degree in chemistry, chemical engineering, biology, microbiology, toxicology, environmental sciences is required.
12+ years of product development, product registration and regulatory affairs experience or a Masters Degree and 10+ years of product development, product registration and regulatory affairs experience
5+ years project management experience

Preferred Qualifications

• PhD in chemistry, chemical engineering, biology, microbiology, toxicology, environmental sciences
• Experience dealing with global regulatory processes and EU Biocidal Products
• Directive (BPD), U.S. EPA, FDA, USDA, OSHA, DOT, and regulatory agencies outside the U.S
• Familiarity with regulatory requirements and standards governing global manufacturing and distribution of chemical , antimicrobial, and pharmaceutical products;
• Ability to represent the company in regulatory matters relating to product registration and environmental health issues;
• Ability to respond quickly in emergency situations relating to regulatory strategy issues, bearing in mind potential reporting requirements and public relations issues;
• Experience in training and teaching various personnel about regulatory requirements and practices;
• Experience with FIFRA-regulated pesticides, antimicrobial pesticides, food additives, topical antiseptic human drugs, and animal drugs.


Compensation
Negotiable