Senior Regulatory Affairs Specialist – CPG Manufacturing – Denver, CO

Are you an expert in regulatory compliance with a passion for the Consumer Packaged Goods (CPG) industry? We are seeking a Senior Regulatory Affairs Specialist to join a fast-growing CPG manufacturing company in Denver, CO. This role offers the unique opportunity to shape compliance strategies, ensure product integrity, and collaborate with cross-functional teams to navigate complex regulatory landscapes. If you have a keen eye for detail and thrive in a dynamic manufacturing environment, this position is for you.

Lead Regulatory Compliance in a Thriving CPG Manufacturing Environment

A leading Consumer Packaged Goods (CPG) manufacturing company in Denver, CO is looking for a Senior Regulatory Affairs Specialist to drive compliance initiatives and support product innovation. The ideal candidate will have a strong background in regulatory affairs, in-depth knowledge of FDA, USDA, and FTC guidelines, and experience ensuring product labels, claims, and marketing materials align with legal requirements. This is your chance to play a pivotal role in bringing safe, high-quality products to market while mitigating compliance risks.

Key Responsibilities of the Senior Regulatory Affairs Specialist – CPG Manufacturing

As a Senior Regulatory Affairs Specialist in the CPG manufacturing industry, you will play a pivotal role in ensuring compliance with all relevant regulations, managing product labeling requirements, collaborating with cross-functional teams, and overseeing regulatory submissions. This role requires a strong understanding of FDA, USDA, FTC, and international regulatory guidelines, as well as the ability to implement effective compliance strategies within a fast-paced consumer goods environment.

🔹 Regulatory Strategy & Compliance:

Develop, implement, and maintain regulatory strategies to ensure that all company products comply with federal, state, and international regulations governing the CPG (Consumer Packaged Goods) industry.
Serve as the regulatory subject matter expert by interpreting and applying regulations from the Food and Drug Administration (FDA), U.S. Department of Agriculture (USDA), Federal Trade Commission (FTC), and other relevant agencies.
Assess the regulatory landscape, identify potential compliance risks, and provide proactive solutions to ensure uninterrupted product commercialization.

🔹 Product Labeling & Claims Review:

Conduct comprehensive reviews of product labels, packaging, and marketing materials to ensure compliance with local, national, and global regulatory standards.
Collaborate with marketing and product development teams to ensure product claims, ingredient listings, and allergen declarations align with regulatory requirements.
Monitor advertising claims, nutritional labeling, and product positioning to prevent misleading or non-compliant representations.

🔹 Cross-Functional Collaboration:

Work closely with R&D, Quality Assurance, Marketing, Legal, and Supply Chain teams to integrate regulatory insights into product innovation and brand strategy.
Provide regulatory guidance throughout the product lifecycle—from concept development to post-market compliance.
Support Quality Assurance teams in ensuring that all manufacturing, testing, and labeling practices adhere to current regulatory requirements.

🔹 Regulatory Submissions & Documentation:

Prepare, submit, and manage all necessary regulatory filings, including but not limited to:
- GRAS notifications
- New product registrations
- Formula approvals
- Ingredient petitions
- Facility registrations and certifications
Maintain meticulous records of regulatory submissions, ensuring that all documentation is accurate, up-to-date, and readily accessible for audits and inspections.
Work with international regulatory bodies for product approvals in global markets, ensuring seamless compliance with import/export regulations.

🔹 Compliance Monitoring & Risk Management:

Continuously monitor emerging regulations, industry trends, and evolving compliance requirements in the CPG and food manufacturing sectors.
Evaluate the impact of regulatory changes on existing products and develop strategies to mitigate risks and maintain compliance.
Conduct internal audits and gap assessments to proactively identify compliance issues before they become critical.

🔹 Audit Preparation & Support:

Lead preparations for regulatory audits conducted by government agencies, certification bodies, and third-party auditors.
Develop audit-ready documentation to demonstrate compliance with all relevant FDA, USDA, and international food safety regulations.
Serve as the primary point of contact during regulatory inspections and audits, ensuring a smooth process and positive outcomes.

🔹 Training & Education:

Develop and deliver regulatory training programs for internal stakeholders, including R&D, marketing, sales, and quality assurance teams.
Keep employees informed of new regulatory requirements, industry best practices, and company policies to foster a culture of compliance.
Provide guidance on the proper interpretation and implementation of food labeling laws, advertising regulations, and ingredient disclosures.

What the Client is Looking for in You

As a Senior Regulatory Affairs Specialist – CPG Manufacturing, the client seeks a proactive professional who excels in navigating regulatory complexities, supports product innovation, and safeguards brand reputation. You should have a solid understanding of the Consumer Packaged Goods (CPG) landscape and the ability to provide strategic regulatory guidance to cross-functional teams.

Proven Expertise in Regulatory Affairs

The client is looking for a candidate with:

✔️ 5+ years of experience in regulatory affairs within the CPG manufacturing industry.
✔️ Deep knowledge of FDA, USDA, FTC, and other applicable CPG regulations.
✔️ Strong experience with product labeling, claims substantiation, and ingredient compliance.
✔️ Familiarity with GRAS notifications, product registrations, and regulatory submissions.

Strategic Thinker with Regulatory Foresight

You must demonstrate the ability to:

✔️ Develop and implement compliance strategies that align with business goals and regulatory requirements.
✔️ Anticipate changes in CPG regulations and provide proactive guidance to leadership teams.
✔️ Collaborate with R&D, Marketing, and Legal teams to balance innovation with compliance.

Detail-Oriented & Collaborative Leader

The ideal candidate will:

✔️ Exhibit meticulous attention to detail in label reviews, product claims, and regulatory filings.
✔️ Work seamlessly with cross-functional teams, ensuring compliance is embedded in every stage of product development.
✔️ Provide clear regulatory advice, empowering teams to make informed decisions.

Commitment to Ongoing Learning & Compliance

You should be passionate about staying up-to-date with evolving CPG regulations and fostering a culture of compliance within the organization.

FAQs About the Role – Senior Regulatory Affairs Specialist – CPG Manufacturing

1. What are the key responsibilities of this role?
As the Senior Regulatory Affairs Specialist, you will oversee regulatory strategies, ensure product compliance with FDA and USDA regulations, review product labels and claims, and collaborate with cross-functional teams. You will also manage regulatory filings, prepare for audits, and educate internal teams about compliance practices.

2. What qualifications are required for this position?
The ideal candidate should have:

5+ years of regulatory affairs experience in CPG manufacturing.
A strong understanding of FDA, USDA, and FTC regulations.
Expertise in product labeling, ingredient compliance, and claims review.
Experience with GRAS notifications and product registrations.

3. How important is cross-functional collaboration in this role?
Extremely important! You will work closely with R&D, Marketing, Quality Assurance, and Legal teams to ensure compliance is integrated into every aspect of product development and marketing strategies.

4. What challenges can I expect in this role?
Expect to navigate evolving CPG regulations, balance product innovation with compliance, and manage multiple projects simultaneously. You’ll need to proactively address potential risks and ensure the company stays ahead of regulatory changes.

5. What impact will I have on the company’s growth?
As the Senior Regulatory Affairs Specialist, you’ll play a vital role in ensuring product integrity, protecting brand reputation, and supporting successful product launches. Your expertise will directly influence the company’s ability to expand into new markets and maintain consumer trust.

What Remuneration Can You Expect from This Job?

As a Senior Regulatory Affairs Specialist – CPG Manufacturing – Denver, CO, you can expect a competitive compensation package that reflects your expertise in regulatory compliance and the critical role you play in ensuring product safety and legal alignment. The remuneration for this role typically includes:

1. Base Salary

The base salary for a Senior Regulatory Affairs Specialist in the CPG manufacturing industry generally ranges between $85,000 to $110,000 annually, depending on your experience, qualifications, and the company’s size and market presence.

2. Performance-Based Bonuses

In addition to your base salary, many companies offer annual performance bonuses tied to key metrics such as regulatory milestones, successful product approvals, and compliance project completions. These bonuses can range from 10% to 20% of your base salary.

3. Equity & Stock Options

For senior roles, some companies—especially publicly traded ones—may offer equity incentives like stock options or restricted stock units (RSUs). This allows you to share in the company’s long-term growth and success.

Certain CPG companies may provide profit-sharing plans or long-term incentives that reward you for contributing to the company’s sustained compliance and innovation strategies. These plans typically kick in after a set period of employment.

5. Comprehensive Benefits

Senior Regulatory Affairs Specialists often receive a robust benefits package, which may include:

Health, dental, and vision insurance
401(k) plans with company matching
Paid time off (PTO) and holidays
Professional development stipends for certifications and conferences
Wellness programs and employee assistance plans (EAPs)

6. Signing Bonuses & Relocation Assistance

For high-demand candidates, some companies may offer signing bonuses or relocation support to ease your transition. These bonuses typically range from $5,000 to $15,000 depending on the company’s policies and your level of expertise.

Total Compensation Potential

When combining your base salary, bonuses, and additional incentives, the total compensation for a Senior Regulatory Affairs Specialist can range from $95,000 to $130,000 annually — with further growth opportunities as you advance within the company.

This package not only reflects your technical and strategic value but also rewards your role in ensuring regulatory excellence and product integrity within the CPG sector.

How to Apply

If you are a seasoned professional with deep expertise in regulatory affairs and a passion for the Consumer Packaged Goods (CPG) manufacturing industry, we invite you to apply for the Senior Regulatory Affairs Specialist position in Denver, CO. This is an exciting opportunity to contribute to the regulatory strategy of a leading CPG company and ensure compliance with industry regulations.

To apply, please submit your resume and a cover letter outlining your experience in regulatory affairs within the CPG manufacturing space. In your cover letter, highlight your knowledge of FDA, EPA, and other relevant regulations, as well as your ability to manage compliance, oversee regulatory submissions, and navigate complex legal requirements. Emphasize your experience in product safety, labeling, and claims management, as well as your ability to collaborate with cross-functional teams to ensure regulatory compliance across all stages of product development and manufacturing.

This role offers an impactful career opportunity where you will play a crucial part in maintaining regulatory compliance, enhancing product safety standards, and ensuring the company’s success in the ever-evolving CPG industry. Apply today to take the next step in your regulatory affairs career as a Senior Regulatory Affairs Specialist in Denver, CO!

For more information or to explore similar opportunities, visit our CPG Regulatory Affairs Jobs Page.

Job Category: CPG Manufacturing

Job Type: Full Time

Job Location: Denver

Senior Regulatory Affairs Specialist – CPG Manufacturing – Denver, CO