9 days old

Regulatory Affairs Specialist

Kelly Services
Chicago, IL 60684
Mid to Senior level Regulatory Specialist position available in the Chicago area.

Opportunity to work with a global company with a long history of providing sustainable food production products.

Fulltime opportunity available, great benefits, education benefits (seminars, continuing education, etc.), retirement ! Internal growth opportunities, several options within your career development.

10% travel within the United States

What we need:

+ Someone with experience in product registrations (US & Canada)

+ Interact with EPA, FDA, DEA

+ Internal teams, R&D ,marketing, food processing plants, external clients

+ Regulatory Specialist

**Job Description:**

We support our customers in reducing their environmental footprint while improving food production, profitability and the well-being of the people and animals involved.

We also supply food production facilities with needed cleaners, sanitizers and disinfectants that comply with EPA regulations.

The Regulatory Specialist, reporting to the Regulatory Affairs Manager Latin and North America, is responsible for preparing, amending, and maintaining product registration dossiers for all product categories within Animal Health (MQAH).

This role will work closely with the Regulatory Affairs Manager Latin America, Product Managers, R&D chemists and Sales team members and take on advanced Regulatory responsibilities as assigned. We are looking for someone who is a quick learner, a self-starter, and is confident to make recommendations/suggestions on regulatory issues in order to move the registration process along.


Responsible for product registrations for North America including state and federal preparation submissions and maintenance of existing registrations, including amendments.

Maintain regular contacts with Regulatory Authorities and regulatory consultants for the follow-up of dossiers, documentation or queries, related to veterinary topical products and hard surfaces detergents/disinfectants.

Manage communications on needed data requirements for new and amended registrations

Liaison with country specific consultants as required (may have specific country responsibility for registrations, etc.).

Review/approve production documentation (i.e. formula, raw material monographs, test methods, etc.) particularly pertaining to product registration dossiers.

Prepare and review clinical trial protocols and review final reports.

Maintain all product registrations for compliance to US and Canada requirements.

**Why Kelly** **** **?**

Kelly Science & Clinical is your connection to premier scientific and clinical companies looking to hire talented people just like you. Every day, we match science professionals with dream jobs that fit their skills and interestsits the way we think job searching should be. Nearly 100 percent of our science recruiters have a professional background/education in science, so we know a thing or two about the science market and how to get you noticed.

**About Kelly** ****

At Kelly, were always thinking about whats next and advising job seekers on new ways of working to reach their full potential. In fact, were a leading advocate for temporary/nontraditional workstyles, because we believe they allow flexibility and tremendous growth opportunities that enable a better way to work and live (plus, did we mention we provide a ton of benefits ?). Connecting great people with great companies is what we do best, and our employment opportunities span a wide variety of workstyles, skill levels, and industries around the world.

Kelly is an equal opportunity employer committed to employing a diverse workforce, including, but not limited to, minorities, females, individuals with disabilities, protected veterans, sexual orientation, gender identity. Equal Employment Opportunity is The Law. (


Posted: 2021-09-13 Expires: 2021-10-14

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Regulatory Affairs Specialist

Kelly Services
Chicago, IL 60684

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