Regulatory Affairs Specialist

Regulatory Affairs Specialist Apply Now Applied To save a job sign in or get started

Job ID:

10209447 Posted today Back Des Plaines, IL, US Scientific Bachelors Degree Full Time, Direct Hire $85,000

• 95,000/year Experienced (Non-Manager) On-site Food and Beverage Production First Shift (Day) Des Plaines, IL, US $85,000
• 95,000/year Experienced (Non-Manager) Full Time, Direct Hire Food and Beverage Production On-site Scientific Bachelors Degree First Shift (Day) Apply Now Applied Job details Kelly Science & Clinical is hiring a Regulatory Affairs Specialist (North America) for a full-time opportunity in Des Plaines, IL.

About the Role In this position, you will support regulatory activities across the U.S. and Canada for a portfolio of products used in animal health and sanitation applications. The role focuses on developing and maintaining regulatory submissions, ensuring compliance with applicable regulations, and collaborating with internal and external stakeholders to support product lifecycle needs. This opportunity is well-suited for a regulatory professional ready to take on broader responsibilities and contribute to strategic regulatory decision-making. What You'll Do Coordinate preparation, submission, and lifecycle management of product registrations at federal and state/provincial levels Maintain compliance for products regulated in the U.S. and Canada, including updates, renewals, and changes Interface with regulatory agencies and third-party consultants to address submission questions and requirements Review technical and manufacturing documentation to ensure alignment with regulatory expectations Assess product labels and promotional materials for regulatory accuracy and compliance Draft and revise Safety Data Sheets (SDS) and support hazard communication requirements Contribute to regulatory listings, licenses, and reporting obligations Review study protocols and summaries related to product performance and safety Monitor regulatory updates and communicate potential impacts to internal stakeholders Partner with cross-functional teams (R D, Quality, Operations, Marketing) to support compliant product development and commercialization Assist in identifying and mitigating compliance risks related to product safety and environmental considerations Support internal and external communications regarding regulatory changes or impacts

Qualifications Education:

Bachelor's degree in Chemistry, Biochemistry, Toxicology, or a related scientific discipline (additional coursework in Animal Science is a plus)

Experience:

Minimum of 3 years in regulatory affairs within industries such as animal health, chemical products, or disinfectants Experience working with agencies such as FDA, EPA, and/or Health Canada Familiarity with product registration processes, technical documentation, and labeling requirements Key Skills Ability to interpret and apply regulatory guidelines and technical information Strong written and verbal communication skills Excellent attention to detail and organizational abilities Proven ability to manage multiple priorities and deadlines Independent problem-solving and decision-making capability Proficiency with Microsoft Office tools (experience with design/layout software is a plus) Preferred Background Knowledge of GLP, GMP, or similar compliance frameworks Experience supporting regulated products such as veterinary treatments or sanitation solutions Exposure to agricultural or animal care industries Familiarity with laboratory or clinical study processes Understanding of certification programs or sustainability-related standards

Additional Details Location:

Des Plaines, IL Travel:

Approximately 10% Take the next step in your regulatory career with Kelly Science & Clinical—apply today to join a collaborative and innovation-driven environment. 10209447 Share this job Copied url To save a job sign in or get started To apply for this job email your details to I want more jobs like this in my inbox.

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