Regulatory Manager
Vibrant Ingredients
Direct message the job poster from Vibrant Ingredients Founded in 1954, Vibrant Ingredients is a leading provider of natural, clean label ingredients and systems that power extraordinary food and beverage experiences. The company’s broad portfolio including natural flavors, botanical extracts, functional nutrition, cold brew coffee, tea essences, and food protection solutions — enhances taste, texture, color, shelf life, and performance across a wide range of applications. Vibrant operates four state-of-the-art facilities across the United States and works with leading brands, manufacturers, and foodservice operators. With vertically integrated capabilities and a proven track record of innovation and execution, Vibrant helps customers accelerate to market without compromise. About the role: We are a trusted partner to our customers when it comes to innovation and an industry leader in clean label ingredients, we are a true partner. We collaborate with our customers in ways that respect people and the environment. A commitment to Purely Better™ drives our innovation team to discover new, on trend solutions. As a Regulatory Manager , you will oversee day-to-day regulatory operations, ensure compliance across assigned product lines, support market-access activities, and lead a team of regulatory professionals. You will partner closely with R&D, Quality, Commercial, and Operations teams to provide regulatory expertise that enables compliant product development, customer support, and operational excellence. How will you contribute: To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. Reasonable accommodation may be made to enable qualified individuals with disabilities to perform essential job functions. Essential job functions and duties include, but are not limited to: Regulatory Operations & Compliance Manage regulatory oversight for assigned portfolios, ensuring compliance with applicable U.S. and international food & flavor regulations (FDA, FEMA, EFSA, CFIA, USDA, TTB). Interpret regulatory requirements for ingredients, formulations, certifications, claims, and labeling. Review and approve standard and moderately complex product documentation, including formulations, labels, and customer regulatory statements. Support regulatory assessments for new product development and ingredient qualification. Serve as the regulatory expert for all flavor ingredients and formulations. Team Management & Development Supervise, mentor, and develop Senior Regulatory Specialists and Regulatory Specialists. Assign workload and maintain clear team priorities aligned with business needs. Support onboarding, training, and continuous development of regulatory staff. Ensure accurate and consistent outputs and support team KPI delivery. Product Documentation & Customer Support Ensure timely preparation and maintenance of regulatory documents (TDS, SDS, allergen/GMO statements, nutritional and natural certifications, NGP forms, Kosher/Halal certs, COO, Prop 65, flavor labeling, TTB submissions, and more). Support global market-entry requirements through certification preparation and regulatory submissions. Support customer requests, audits, documentation portals, and documentation reviews. Provide compliance guidance to internal teams to support product development and commercialization. Regulatory Intelligence & Process Improvement Monitor regulatory changes and industry updates impacting flavors, ingredients, and consumer products. Communicate regulatory updates internally and recommend appropriate actions. Drive improvements in regulatory systems, digital tools, and documentation workflows. Support audit, inspection, and compliance review preparation. Cross-Functional Collaboration Partner with R&D, Quality, Procurement/Supply Chain, Marketing, and Sales to ensure compliant product development and ingredient qualification. Serve as a regulatory subject-matter expert in cross-functional meetings. Collaborate with customers and regulatory agencies to resolve regulatory issues. Minimum Requirements/Qualifications: Bachelor’s degree in Food Science, Quality, Biology, Biotechnology, Chemistry, or related field. 6+ years of flavor industry experience; additional food, ingredients, or consumer goods experience preferred. Working knowledge of global food and flavor regulations (FDA, FEMA GRAS, USDA, CFIA, EU, Organic, Kosher, Halal, TTB, labeling, import/export). Experience with Rainforest Alliance, Fair Trade, and Non-GMO Verification Project preferred. Knowledge of Dietary Supplements, AAFCO, and IFRA a plus. Experience supporting innovation pipelines and new product development from a regulatory perspective. Preferred Qualifications Strong regulatory interpretation and problem-solving capabilities. Demonstrated leadership, coaching, and decision-making skills. Excellent communication skills with the ability to translate regulatory requirements for both technical and non-technical audiences. Highly organized and capable of managing multiple concurrent projects. Strong cross-functional influence with a compliance-driven mindset. Proficiency in MS Office and regulatory database systems; experience with Salesforce and Product Vision preferred; Business Central a plus. May involve exposure to allergens such as Soy, Wheat, Fish, Shellfish, Milk, Egg, Tree Nuts and Sesame. What Vibrant Ingredients can offer you: Generous time off for vacations Paid Holidays 401(k) with company match Health & Wellness programs This position is currently classified as on-site. Employees are eligible to participate in Medical, Dental, Vision, Life Insurance, 401(k), Holidays, Vacation, Tuition Reimbursement Program. EEO Statement Vibrant Ingredients is an equal opportunity employer committed to employing a diverse workforce and providing accommodations for people with disabilities in all parts of the hiring process as required under its Employment Accommodation Policy. Vibrant Ingredients will work with applicants to meet accommodation needs that are made known to Vibrant Ingredients in advance. #J-18808-Ljbffr Vibrant Ingredients
- A leading provider of natural ingredients in New Jersey seeks a Regulatory Manager to oversee day-to-day regulatory operations and ensure compliance across product lines. The role requires a Bachelor's degree in Food Science and 6+ years in the flavor industry. Strong...Suggested
- Director, Renewable Fuels Compliance & Regulatory Advisory Business Development Cranbury, NJ ID: 447-390 Full-Time/Regular Job Summary... ...project profitability. Design and implement complete compliance management systems, including regulatory reporting processes, data...SuggestedFull timeContract workWork at officeRemote work
- ...years in the pharmaceutical industry, preferably with 1 year CMC regulatory experience Responsibilities will include, but are not... ...CMC change controls with supervision. 4. Responsible for the management of CMC activities related to developmental or commercial compounds...Suggested
- ...Regulatory Specialist (East Windsor, NJ) (Multiple Openings). Review, manage and write regulatory submissions electronically which include New ANDA filings, Complete Response letters, Information requests, Amendments to the ANDA’s (Labeling, Chemistry & Bioequivalence...Suggested
$100k - $180k
...is seeking an Associate Director for Quality Assurance in Cranbury, NJ. This role focuses on establishing and improving Quality Management Systems supporting GMP clinical manufacturing. Successful candidates will have extensive experience in the pharmaceutical industry...Suggested- AmSpec seeks a Director of Renewable Fuels Compliance & Regulatory Advisory in Cranbury, NJ. The role leads regulatory compliance programs... ...multidisciplinary team delivering ongoing advisory services while managing regulatory risk and profitability. #J-18808-Ljbffr AMSPEC
- Porton Pharma Solutions Ltd. in Cranbury, NJ is seeking an experienced Environmental, Health, and Safety (EHS) Manager to lead our EHS initiatives within our CDMO operations. The ideal candidate will ensure compliance with local, state, and federal regulations while fostering...Local area
$70.4k - $123.2k
...is looking for a PRB Specialist based in Plainsboro Township, NJ. This role involves collaboration with marketing operations and managing the planning and review process of promotional materials. Candidates should have a Bachelor’s degree and at least 3 years of relevant...Flexible hours$160k - $260k
...in ensuring the highest standards of professional excellence, regulatory adherence and quality within the business, with overall responsibility... ...sites collaboration and leadership execution for WuXi Quality Management System, inclusive of GMP standards, compliance programmes. A...Work experience placementLocal area- ...Job Details: Clinical Regulatory Affairs Manager An innovative technology company is seeking an experienced Clinical Regulatory Affairs Manager to support regulatory strategy, clinical initiatives, and product development activities for advanced healthcare technologies...Flexible hours
$145.6k - $279.4k
...S. work visa sponsorship is not available for this role now or in the future. Job Description Leads and manages the preparation, review, and submission of regulatory applications, including product registrations, progress reports, supplements, amendments, and periodic experience...Work at officeRemote workRelocation packageFlexible hours- ...will be the day-to-day contact for all sampling activities within the Dermatology team. The role emphasizes PDMA compliance, vendor management, and cross‑functional collaboration to align sampling programs with product launches and commercial initiatives. Prior experience...
- ...comprehensive compliance program that supports ethical, legal, and regulatory practices across all operations at APluscare. This role... ...Lead and oversee the development, implementation, and ongoing management of the organization’s compliance program across all services,...Flexible hours
- ...multiple clinical programs spanning early and late-stage development and an expanding global footprint, they are seeking an experienced Regulatory Affairs leader to shape worldwide regulatory strategy and accelerate the development of breakthrough cancer therapies. This is a...Worldwide
$180k - $225k
...experienced Associate Director, Advertising & Promotions to join our Regulatory Affairs team. The Associate Director, Regulatory Affairs... ...regulatory advice, leading complex promotional reviews, managing FDA submission requirements and improving review processes. The...Full timeWork at office- ...Investigo client is seeking a senior Regulatory Affairs leader to shape worldwide regulatory strategy for oncology programs, spanning early development through commercialization. You will interact with FDA, EMA, PMDA, and NMPA, guiding global filings and regulatory strategy...Worldwide
- ...13485 certified. We are strengthening our U.S.-based quality management system and integrating global operations as we transition from... ...expansion. Position Summary: We are seeking an experienced Senior Regulatory Affairs & Quality Systems Manager to lead FDA 510(k) and CLIA...Overseas
$160k - $260k
WuXi Biologics is seeking a US GMP Compliance Head to ensure cGMP compliance across US sites. The role involves managing a compliance team, leading regulatory inspections, and collaborating closely with quality heads. Ideal candidates should have a degree in...- Novo Nordisk A/S in Plainsboro, NJ is seeking a Market Access Employer Strategy Director to lead the employer channel strategy and cross-functional execution for GLP-1 access and obesity therapies. You will partner with MAPA, payer organizations, brokers, and health plans...
- ...reports to the Executive Senior Associate Athletic Director. This position will have oversight of a staff member and assist with management of day-to-day operations in conjunction with peer Associate AD. Among the key duties of the position are the following: Manages all...Part timeWork at office
- ...presence in the Life Science market sector in New Jersey. Lead a Regulatory Compliance Validation team for pharmaceutical, biotech and... ...increasing responsibility in validation/quality service and project management of life sciences, biotech or other FDA regulated projects....Work at office
- ...QA Manager A Few Words About Us Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well... ...establish a scientific approach to the company quality and regulatory system. • Ensure all GMP, GLP, GCP operations are in compliance...
- Responsibilities Provide strategic leadership for Regulatory Affairs, overseeing NDAs and ANDAs across the full product lifecycle, including... ...strategies to support timely approvals and lifecycle management of assigned products. Oversee the preparation, review, and approval...Contract work
- Rising Pharma Holdings Inc in New Jersey seeks a Senior Regulatory Affairs Leader to drive FDA submissions, regulatory strategy, and lifecycle management across NDA/ANDA programs. You will supervise regulatory operations and labeling, ensure compliance, and partner with...
$120k - $140k
...implementation, evaluation and improvement of program services; management of staff and the delivery of high-quality service to the... ...maintains ongoing compliance with appropriate local, state, federal, regulatory, and/or accrediting body standards. Key Responsibilities...Full timeLocal area- A global staff augmentation firm is looking for a qualified candidate in Plainsboro, NJ to ensure the scientific accuracy and clinical appropriateness of promotional materials. Responsibilities include reviewing promotional pieces, collaborating with stakeholders, and staying...Contract workWork at office3 days per week
$135k - $185k
...The role is accountable for advancing operational excellence, regulatory compliance, workforce engagement, and financial stewardship within... .... · Oversee operating and capital budgets while proactively managing financial performance. · Ensure compliance with hospital...Local areaFlexible hours- ...& Cosmetics in Cranbury Township, NJ is seeking a qualified individual to oversee outbound shipping operations. The role involves managing a team of Traffic Clerks and ensuring compliance with shipping requirements. The ideal candidate should have 2-5 years of relevant...
- A leading medical technology company in Princeton is seeking an Export Trade Compliance Specialist. This role ensures compliance with U.S. Customs and FDA regulations for imports and exports. The specialist will focus on tariff code validation and support broader compliance...
$61.44k - $84.48k
...Job Summary This position will determine the current regulatory requirements and strategies for Terumo’s devices and projects and define... ...and a historical record for projects and provide management with updated product status. Maintains current knowledge of Federal...Temporary workWorldwide
Do you want to receive more vacancies?
Subscribe and receive similar vacancies to Regulatory Manager. Be the first to apply!

