Associate Director, RegulatoryScientific Affairs and Quality

Kemin Health is hiring an Associate Director of Regulatory/Scientific Affairs and Quality! In this role you will be responsible for leading the business units regulatory affairs (RA) and quality assurance (QA) teams by proactively identifying and managing regulatory/quality risks and opportunities aligned with strategic direction and priorities of the business.

This individual will be responsible for overseeing product compliance and registrations at state national and international levels. They will monitor and influence regulatory changes support product safety substantiate claims and ensure label compliance. Additionally they will provide guidance throughout all stages of innovation and commercialization support global customers on regulatory and quality-related matters and ensure the quality compliance of the business units product portfolio globally.

This position is based at our Worldwide Headquarters in Des Moines Iowa. Relocation assistance may be available to candidates outside of a commutable distance.

Join the Kemin Team and Transform Lives!

We are a privately held family-owned-and-operated global biotechnology company driven by curiosity and committed to transforming the quality of life for people pets and the planet.

We create solutions that strengthen health and wellbeing provide nutrition and immune support for pets and production animals safeguard the planets natural resources and protect the global food supply chain for generations to come.

We supply over 500 specialty ingredients for various industries including human and animal health and nutrition pet food aquaculture nutraceutical food technologies crop technologies textiles biofuels and animal vaccines.

We employ 3500 global employees and operations in 90 countries including manufacturing facilities in Belgium Brazil China Egypt India Italy San Marino Singapore South Africa and the United States.

As a valued member of our team youll enjoy a comprehensive benefits package designed to support your financial physical and professional well-being:

• Competitive Financial Package: Enjoy a rewarding salary uncapped bonus opportunities a 401k match program and generous paid vacation and holidays.
• Health and Wellness Support: Stay fit and healthy with our fitness reimbursement for the whole family access to an on-site fitness center a restaurant offering seasonal fresh food options and free fresh fruit in break areas.
• Career Development and Advancement: Unlock your potential with opportunities for growth and development throughout your entire career.
• Continued Learning Opportunities: Grow your skills with our in-house learning platforms offering thousands of training resources both live and online and take advantage of tuition reimbursement for external post-secondary pursuits.
• Service Opportunities: Make a positive impact with paid time off for service partnerships with The World Food Programme and Habitat for Humanity and local community initiatives.

• Responsible for leading and establishing direction for the business unit Regulatory Affairs (RA) and Quality Assurance (QA) department and working cross-functionally across business units and within the business unit to assure regulatory and quality compliance for the products marketed and sold by the primary business unit.
• Responsible for establishing and managing the RA/QA budget and departmental strategies to support the overall strategic plan
• Work cross-functionally and provide regulatory scientific and quality expertise and support through all stages of the innovation process ensuring the safety freedom-to-operate and regulatory compliance of ingredients contaminant legislations and packaging materials.
• Ensure that Kemin Health ingredients formulas products labels packaging promotional materials and marketing communications comply with relevant local and global regulations as well as Kemin policies and guidelines in collaboration with Commercial and R&D departments.
• Lead and execute on regulatory innovative strategies for Kemin products deemed necessary to achieve business outcomes such as global regulatory approvals and clearance for Kemin Health ingredients labels and claims.
• Serve as official Kemin liaison to regulatory entities including but not limited to US FDA EFSA Health Canada ANVISA etc.
• Responsible for final review and approval of all product formulas as well as review of commercial collateral administered through Kemins Permission to Publish (PTP) program.
• Support Kemin Health customer needs and/or create collateral related to regulatory claims and quality compliance as it related to Kemin Health ingredients.
• Oversee QA for all Kemin Health products including food safety and regulatory compliance programs and systems (HACCP GMP Environmental Monitoring Pest Control and Sanitation Program; hold and reject; product recovery allergens recalls and inspections (internal and external).
• Oversee and work closely with Central Operations and Quality on audits (regulatory and customer) supplier qualification non-compliant product and consumer complaints.
• Oversee quality certifications including Kosher Halal and non-GMO Project Verification.
• Stay abreast of the changing regulatory legal quality and competitive landscape.
• Assess and prepare in-depth regulatory assessments and opinions as it relates to evolving business needs.
• Responsible for final review and approval of all product formulas and product claims quality questions and claim-language freedom to operate decisions for business unit product portfolio
• Determine regulatory requirements and interpret relevant government regulations to support the business unit product portfolio. Demonstrates servant leadership in all aspects of managing the RA/QA department including performance discussions managing priorities hiring of staff.

• Education & Experience:
  • Undergraduate degree with 10 years of experience in dietary ingredients nutraceuticals or food ingredient company
  • OR an advanced degree in science or legal field with at least 5 years of experience in dietary ingredients nutraceuticals or food ingredient company
• Strong experience and understanding of U.S. (State and Federal) and relevant global laws and regulations in key regions (EU Canada Mexico Brazil APAC Australia) as they relate to dietary ingredients including but not limited to ingredient manufacturing safety contaminants quality packaging/labels claims and claim substantiation.
• Experience with supporting customers on regulatory and quality-related matters.
• Experience and knowledge/skills related to Quality Management Systems such as GMPs ISO HACCP
• Must have excellent time management and organization skills a high energy level and a sense of commitment and urgency to ensure obligations are met.
• Excellence in presenting influencing fostering relationships across global cultures
• Ability to lead and develop people previous experience managing people required.
• Experience working with variety ofgovernment agencies.
• Experience in drafting and assembling successful regulatory dossiers that result in approval/market clearance by the US and/or foreign regulatory authorities.
• Strategic and business-impact mindset.
• Ability to influence articulate and propose alternatives to critical decisions without compromising quality and safety.
• Travel up to 20% including both regional and global.

We are an equal opportunity employer. We consider all qualified applicants without regard to race color creed/religion national origin ancestry citizenship or immigration status (where applicable) sex sexual orientation gender identity or expression pregnancy/childbirth/breastfeeding or related conditions age (40) disability (including the use of a service animal) genetic information marital status familial or caregiver status military or veteran status status as a victim of domestic violence reproductive health decisionmaking and any other status protected by applicable federal state or local law. We also prohibit retaliation for raising concerns or participating in an EEO process. Applicants who need a reasonable accommodation to apply or interview can email .

A post-offer background check and drug screen is required. Additional pre-employmentrequirementsmay be necessarybased onposition.

Kemin is a drug-free and tobacco-free campus.

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