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Quality Regulatory Manager Jobs in Delaware (NOW HIRING)

Iff

Associate Manager, Regulatory Affairs

Wilmington, DE · On-site

Partner closely with Research & Development (R&D), Applications, Quality, and Commercial teams to ... Hands-on experience preparing and managing regulatory submissions, notifications, and supporting ...

New

Hologic

Sr Manager, Regulatory Operations

Newark, DE · On-site

Partner with Quality and Commercial teams to support timely product launches, updates, and changes. * Lead regulatory post-market summary reporting activities including managing timely submission of ...

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Quality Regulatory Manager information

What is a quality regulatory manager?

A Quality Regulatory Manager is a professional responsible for ensuring that a company's products and processes comply with industry regulations, standards, and quality requirements. They oversee the implementation of quality management systems, prepare for regulatory audits, and keep the organization updated on changing regulations. This role often involves working closely with various departments to ensure documentation, processes, and products meet both internal and external compliance standards. Quality Regulatory Managers play a critical part in maintaining the company's reputation and ability to operate within legal guidelines.

How does a quality regulatory manager typically collaborate with cross-functional teams to ensure compliance?

A Quality Regulatory Manager works closely with departments such as manufacturing, R&D, and supply chain to interpret and implement regulatory requirements across the organization. Regular meetings and clear communication are essential to align quality systems with evolving regulations and address compliance gaps. The manager often leads training sessions, reviews documentation, and coordinates audits, ensuring all teams understand and adhere to quality standards. This collaborative approach helps maintain product safety and supports successful regulatory submissions.

What are the key skills and qualifications needed to thrive as a quality regulatory manager, and why are they important?

To thrive as a Quality Regulatory Manager, you need in-depth knowledge of quality management systems, regulatory compliance, and industry standards, typically backed by a relevant degree and experience in regulated environments. Familiarity with ISO standards, FDA regulations, audit management tools, and certifications like CQE or RAC is highly valued. Strong analytical thinking, attention to detail, and effective communication are critical soft skills for collaborating across departments and ensuring compliance. These skills and qualifications are essential to maintain product quality, meet regulatory requirements, and mitigate compliance risks within an organization.

What is the difference between Quality Regulatory Manager vs Quality Assurance Specialist?

AspectQuality Regulatory ManagerQuality Assurance Specialist
CertificationsISO 13485, Regulatory Affairs certificationsISO 9001, QA certifications
Work EnvironmentRegulatory agencies, compliance departmentsManufacturing, production, quality labs
Employer & Industry UsageMedical devices, pharmaceuticals, biotechManufacturing, consumer products, electronics

The Quality Regulatory Manager focuses on ensuring products meet regulatory standards and manages compliance documentation, often working closely with regulatory agencies. In contrast, the Quality Assurance Specialist primarily ensures product quality through testing and process audits. Both roles require quality certifications but differ in their focus areas and work environments.

What are popular job titles related to Quality Regulatory Manager jobs in Delaware?

For Quality Regulatory Manager jobs in Delaware, the most frequently searched job titles are:

What job categories do people searching Quality Regulatory Manager jobs in Delaware look for?

The top searched job categories for Quality Regulatory Manager jobs in Delaware are:

What cities in Delaware are hiring for Quality Regulatory Manager jobs?

Cities in Delaware with the most Quality Regulatory Manager job openings:

Quality Regulatory Manager jobs near you
Infographic showing various Quality Regulatory Manager job openings in Delaware as of August 2026, with employment types broken down into 1% As Needed, 79% Full Time, 15% Part Time, 4% Contract, and 1% Nights. Highlights an 84% Physical, 1% Hybrid, and 15% Remote job distribution.

Associate Manager, Regulatory Affairs

Iff

Wilmington, DE • On-site

Full-time

Posted 2 days ago

New

Job description

Job Summary

IFF is a global leader in flavors, fragrances, food ingredients, and Health & Biosciences, delivering sustainable innovations that elevate everyday products.
Our Health & Biosciences team channels a passion for nature and bioscience into sustainable, life-enhancing technologies that power innovative solutions across healthcare, food, consumer, and industrial markets.
This role is based in ither Madison, Wisconsin or Wilmington, DE. Be part of a creative, solution-oriented team where together we can achieve greatness and make a real impact. Your potential is our inspiration.
Where You'll Make a Difference
  • Serve as the North American regulatory subject matter expert for Food Biosciences products, including food enzymes and cultures, and proactively assess regulatory developments and business impact.
  • Develop and execute regulatory strategies that support commercialization, innovation, and business growth across the United States and Canada.
  • Lead, prepare, and support regulatory submissions and notifications, including Generally Recognized as Safe (GRAS) submissions and Health Canada filings.
  • Partner closely with Research & Development (R&D), Applications, Quality, and Commercial teams to ensure regulatory requirements are integrated into product development and launch activities.
  • Provide timely and accurate regulatory guidance to internal stakeholders and external customers regarding product compliance, regulatory status, and market requirements.
  • Monitor and maintain ongoing compliance of marketed products within North American regulatory frameworks and applicable industry standards.
  • Evaluate regulatory risks and recommend practical, business-focused solutions that support both compliance and innovation.
  • Build and maintain productive relationships with regulatory authorities, industry associations, and external stakeholders to support advocacy and regulatory intelligence.
  • Contribute to regulatory process improvements, documentation practices, and knowledge-sharing initiatives across the broader regulatory organization.\
What Makes You the Right Fit
  • Master's degree in Food Science, Chemistry, Biology, Toxicology, Regulatory Affairs, or a related scientific discipline.
  • Significant regulatory affairs experience within food ingredients, biotechnology, dairy, enzymes, cultures, or another regulated industry.
  • Strong knowledge of United States and/or Canadian regulatory frameworks applicable to food ingredients and Food Biosciences products.
  • Hands-on experience preparing and managing regulatory submissions, notifications, and supporting documentation.
  • Proven ability to interpret and apply complex regulatory requirements to business and product-specific situations.
  • Strong attention to detail, documentation practices, and organizational skills.
  • Excellent communication, collaboration, and stakeholder-management skills, with the ability to influence across functions and levels.
  • Experience working successfully within a global, matrixed organization and collaborating across cultures and regions.
How Would You Stand Out?
  • Experience supporting enzyme, culture, fermentation, biotechnology, or dairy-related product portfolios.
  • Established relationships with North American regulatory authorities, industry associations, or external scientific networks.
  • Demonstrated ability to navigate ambiguity and develop creative, solution-oriented approaches to regulatory challenges.
Why Choose Us?
  • Help bring innovative Food Biosciences solutions to market while ensuring compliance and consumer trust.
  • Partner with global experts across Regulatory Affairs, Research & Development, Quality, and Commercial teams.
  • Influence regulatory strategies that directly support business growth and innovation.
  • Gain exposure to a broad portfolio of food ingredients, enzymes, cultures, and biotechnology solutions.
  • Work in a collaborative, science-driven environment that encourages learning and professional development.
  • Be part of a company committed to creating sustainable solutions that improve everyday life.

We are a global leader in taste, scent, and nutrition, offering our customers a broader range of natural solutions and accelerating our growth strategy. At IFF, we believe that your uniqueness unleashes our potential. We value the diverse mosaic of the ethnicity, national origin, race, age, sex, or veteran status. We strive for an inclusive workplace that allows each of our colleagues to bring their authentic self to work regardless of their religion, gender identity & expression, sexual orientation, or disability.

Visit IFF.com/careers/workplace-diversity-and-inclusion to learn more

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