Brenntag

Regulatory Compliance Specialist - Nutrition

Brenntag  •  Wayne, NJ (Onsite)  •  6 days ago
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Job Description

Your Role & Responsibilities

The Regulatory Compliance Specialist supports the daily operations of the Regulatory Compliance and Document Management function within Brenntag’s Quality and Regulatory organization. This role ensures that product setup, supplier documentation, and TraceGains workflows are executed accurately and efficiently to maintain compliance across Brenntag’s North American portfolio.

The Specialist collaborates cross-functionally with Quality Assurance, Product Management, Regulatory Affairs, and Operations to ensure all regulatory and documentation activities are performed in alignment with internal standards, customer expectations, and applicable regulations. This position plays a key role in maintaining data integrity and document accuracy within Brenntag’s systems to support compliant, timely, and customer-ready operations.

Documentation Management and Product Setup

  • Support the creation, activation, and maintenance of product profiles in TraceGains and internal ERP systems.
  • Link supplier documentation and ensure all required records are associated with approved products.
  • Review incoming documentation for completeness, accuracy, and regulatory compliance prior to approval.
  • Assist in the coordination of product setup, approval, and inactivation processes, ensuring consistency across systems.
  • Maintain version control and traceability of product-related documentation.

Supplier Documentation and TraceGains Oversight

  • Request, track, and review supplier documents (e.g., SDS, statements, questionnaires) to ensure compliance with Brenntag and regulatory requirements.
  • Monitor document expirations and proactively follow up with suppliers to prevent gaps in compliance.
  • Route documents through TraceGains workflows for review and approval according to established procedures.
  • Support document audits and contribute to continuous improvement of document turnaround and accuracy metrics.

Regulatory Requests and Customer Support

  • Assist in the resolution of internal and external regulatory documentation requests, ensuring timely and accurate responses.
  • Assisting the group with complex documentation inquiries and projects.
  • Provide internal support during audits or customer inquiries by ensuring documentation readiness and accessibility.

Change Management and Regulatory Support

  • Assist in reviewing supplier change notifications and evaluating potential impacts on product specifications or documentation.
  • Support updates to product data and specifications resulting from regulatory, supplier, or internal changes.
  • Contribute to maintaining compliance with FDA, Health Canada, and related frameworks through accurate recordkeeping and collaboration with management.

Systems and Process Optimization

  • Ensure alignment between TraceGains, ERP, and SharePoint systems for accurate data traceability.
  • Participate in documentation improvement initiatives and recommend enhancements to digital workflows.
  • Support training activities related to documentation management, system use, and regulatory requirements.
  • Other duties as assigned.

Your Profile

Qualifications and Skills

  • Bachelor’s degree in Regulatory Affairs, Food Science, Chemistry, Biology, or a related scientific discipline.
  • Minimum 5 years of experience in regulatory compliance, documentation management, or quality assurance within food, nutrition, chemical, or related industries.
  • Working knowledge of North American regulatory frameworks.
  • Experience using documentation management systems such as TraceGains, SharePoint, or ERP platforms.
  • Strong organizational skills, attention to detail, and ability to manage multiple priorities.
  • Excellent written and verbal communication skills.
  • Proficient in Microsoft Office Suite (Excel, Word, Outlook, Teams).
  • Demonstrated ability to collaborate effectively across functions in a remote, fast-paced environment.

Our Offer

  • We aim to create an environment where the best people want to work, where they can turn their passion into their job and realize their full potential.

  • Individual development, on-the-job training, and development programs designed to help our employees grow in their careers.

  • Paid parental leave

  • Education assistance program

  • Employee assistance program

  • Various healthcare plan options as well as 401(k)

Brenntag and its subsidiary companies will provide equal employment opportunities to all applicants without regard to any category protected by federal, state or local law, including as applicable, applicant’s actual or perceived race, color, religion, creed, sex, sexual orientation, gender identity or expression (including transgender status), gender (including pregnancy, childbirth, lactation and related medical condition), genetic information, military service, national origin, ancestry, citizenship status, age, veteran status, physical or mental disability, protected medical condition as defined by applicable federal, state or local law, political affiliation, marital status, membership in an employee organization, parental status, expunged juvenile record, or any other status protected by federal, state, or local law. Brenntag will provide reasonable accommodations to allow an applicant to participate in the hiring process (e.g., accommodations for a test or job interview) if so requested. When completing this application, you may exclude information that would disclose or otherwise reference your race, religion, age, sex, genetic, veteran status, disability or any other status protected by federal, state, or local law. This application is considered current for sixty (60) days only. At the end of this period, if you are still interested in employment, it will be necessary for you to reapply by completing a new application.

If you are a qualified individual with a disability or a disabled veteran, you may request a reasonable accommodation if you are unable or limited in your ability to access job openings or apply for a job on this site as a result of your disability. You can request reasonable accommodations by contacting Human Resources at accommodations@brenntag.com (phone, tty, fax, email, etc.).

Brenntag North America, Inc. and its subsidiaries use E-Verify, a government-run, web-based system that allows employers to confirm the eligibility of their employees to work in the United States. For more information, please go to https://www.e-verify.gov/employees or view the poster at https://e-verify.uscis.gov/web/media/resourcesContents/E-Verify_Participation_Poster.pdf

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Brenntag

About Brenntag

Brenntag is the global market leader in chemicals and ingredients distribution and holds a central role in connecting customers and suppliers of the chemical industry. Headquartered in Essen, Germany, we have more than 18,100 employees worldwide and operate a network of around 600 sites in more than 70 countries. In 2024, the company generated sales of €16.2 billion.

The two global divisions, Brenntag Essentials and Brenntag Specialties, provide a diversified and broad portfolio of industrial and specialty chemicals and ingredients as well as tailor-made application, marketing and supply chain solutions, technical and formulation support, comprehensive regulatory know-how and digital solutions for a wide range of industries.

Brenntag pursues an ambitious sustainability agenda and is committed to sustainable solutions in its own sector and the industries served. Brenntag SE shares have been listed on the Frankfurt Stock Exchange since 2010 and have been part of the DAX since September 2021. In addition, the Brenntag SE shares are listed in the DAX 30 ESG and DAX ESG Target.

Industry
Chemicals & Materials
Company Size
10,000+ employees
Headquarters
Essen , DE
Year Founded
Unknown
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