Regulatory Affairs Manager
$90k - $115kActalent
Regulatory Affairs Specialist – Food & FlavorThis role leads regulatory oversight for a defined portfolio of food and flavor products, ensuring full compliance with U.S. and international regulations. The position serves as the regulatory expert for flavor ingredients and formulations, interprets complex regulatory requirements, and provides clear guidance on ingredients, formulations, certifications, claims, and labeling. The role also manages and develops a small regulatory team, improves regulatory systems and processes, and supports internal stakeholders and customers throughout the product lifecycle.ResponsibilitiesProvide regulatory oversight for assigned product portfolios to ensure compliance with applicable U.S. and international food and flavor regulations, including FDA, FEMA, EFSA, CFIA, USDA, and TTB.Interpret regulatory requirements for ingredients, formulations, certifications, claims, and labeling, and translate them into practical guidance for internal teams.Review and approve standard and moderately complex product documentation, including formulations, labels, and customer regulatory statements, to ensure accuracy and compliance.Serve as the regulatory expert for all flavor ingredients and formulations, supporting new product development and ingredient assessments.Supervise, mentor, and develop Senior Regulatory Specialists and Regulatory Specialists, providing coaching and performance feedback.Assign workload across the regulatory team and maintain clear priorities aligned with business needs and project timelines.Support onboarding, training, and continuous development of regulatory staff to build and maintain strong regulatory capabilities.Ensure accurate, consistent, and timely regulatory outputs from the team and support delivery of team key performance indicators (KPIs).Oversee the preparation, review, and maintenance of regulatory documents, including TDS, SDS, allergen and GMO statements, nutritional and natural certifications, Non-GMO Project forms, Kosher and Halal certifications, certificates of origin (COO), Prop 65 documentation, flavor labeling, TTB submissions, and related materials.Support global market-entry requirements by preparing certification packages and regulatory submissions for international markets.Respond to and support customer requests, audits, documentation portals, and documentation reviews with accurate and timely regulatory information.Provide clear compliance guidance to internal teams, including R&D, Quality, Procurement/Supply Chain, Marketing, and Sales, to support product development and commercialization.Monitor and interpret regulatory changes and industry updates impacting flavors, ingredients, and consumer products.Communicate relevant regulatory updates internally and recommend appropriate actions to maintain compliance and support business objectives.Drive continuous improvements in regulatory systems, digital tools, and documentation workflows to increase efficiency, accuracy, and traceability.Support preparation for audits, inspections, and internal or external compliance reviews.Partner with cross-functional teams such as R&D, Quality, Procurement/Supply Chain, Marketing, and Sales to ensure compliant product development and ingredient selection.Act as a regulatory subject-matter expert in cross-functional meetings, providing risk assessments and compliance recommendations.Collaborate with customers and regulatory agencies, as appropriate, to resolve regulatory questions and issues.Essential SkillsExperience in regulatory affairs within the flavor industry, with additional experience in food, beverage, ingredients, or related consumer goods considered a strong asset.Bachelor's degree in Food Science, Quality, Biology, Biotechnology, Chemistry, or a related scientific field.Working knowledge of global food and flavor regulations, including FDA, FEMA GRAS, USDA, CFIA, EU requirements, Organic, Kosher, Halal, TTB, labeling, and import/export regulations.Proven ability to interpret and apply regulatory requirements to ingredients, formulations, certifications, claims, and labeling.Demonstrated experience reviewing and approving product documentation such as formulations, labels, and customer regulatory statements.Capability to supervise, mentor, and develop regulatory professionals, including assigning workload and setting priorities.Strong organizational skills with the ability to manage multiple projects, meet deadlines, and support team KPI delivery.Excellent written and verbal communication skills for preparing documentation, responding to customer requests, and communicating regulatory updates internally.Proficiency with regulatory documentation such as TDS, SDS, allergen and GMO statements, nutritional and natural certifications, Non-GMO Project forms, Kosher and Halal certifications, certificates of origin, Prop 65 documentation, and TTB submissions.Additional Skills & QualificationsExperience in the flavor industry is strongly preferred; experience in food and beverage, ingredients, or related consumer goods is a plus.Familiarity with FEMA and FDA flavor and food regulations.Experience with Rainforest Alliance, Fair Trade, and Non-GMO Project Verification is preferred.Knowledge of IFRA requirements is a plus.Knowledge of dietary supplement regulations, AAFCO guidelines, and IFRA standards is advantageous.Comfort working with digital regulatory systems, documentation portals, and process improvement initiatives.Strong collaboration skills and the ability to work effectively with R&D, Quality, Procurement/Supply Chain, Marketing, Sales, customers, and regulatory agencies.Work EnvironmentThis is an on-site role with the potential for one day per week of remote work, depending on business needs. The position operates in a professional office and laboratory-oriented environment within the food and flavor industry, collaborating closely with world-renowned flavor experts and cross-functional teams. Work involves extensive use of digital regulatory systems, documentation tools, and customer portals, as well as participation in meetings to support product development, commercialization, and compliance activities.Job Type & LocationThis is a Permanent position based out of Monroe, NJ.Pay and BenefitsThe pay range for this position is $90000.00 - $115000.00/yr. Generous time off for vacations Paid Holidays 401(k) with company match Tuition reimbursement Medical/Dental/Vision Health & Wellness programsWorkplace TypeThis is a fully onsite position in Monroe, NJ.Application DeadlineThis position is anticipated to close on Apr 25, 2026.Diversity, Equity & InclusionAt Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I is embedded into our culture through:Hiring diverse talentMaintaining an inclusive environment through persistent self-reflectionBuilding a culture of care, engagement, and recognition with clear outcomesEnsuring growth opportunities for our peopleActalent is an equal opportunity employer.About ActalentActalent is a global leader in engineering and sciences services. For more than 40 years, we've helped visionary companies advance their goals. Headquartered in the United States, our teams span 150 offices across North America, EMEA, and APAC—with four delivery centers in India led by 1,000+ extraordinary employees who connect their passion with purpose every day.Our Bangalore, Hyderabad, Pune, and Chennai delivery centers are hubs of engineering expertise, with core capabilities in mechanical and electrical engineering, systems and software, and manufacturing engineering. Our teams deliver work across multiple industries including transportation, consumer and industrial products, and life sciences. We serve more than 4,500 clients, including many Fortune 500 brands. Learn more about how we can work together at actalentservices.com.
- ...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...Suggested
- The Regulatory Specialist is an on-site role responsible for ensuring that products, ingredients... ...regulatory requirements. This role manages regulatory documentation, product registration... ...Compliance Support the Regulatory Affairs Manager in ensuring compliance with...SuggestedWork at office
- ...JOB SUMMARY This will person will be a Regulatory liaison between product development and... ...letters/information requests.• Independently manage preparation (in paper or electronic... ...experience in pharmaceutical regulatory affairs (mandatory)• Attention to detail• Excellent...Suggested
$340k - $420k
The VP/SVP, Head of Regulatory Affairs will provide strategic and operational leadership for the Company’s global regulatory function and serve... ..., from early development through registration and lifecycle management. The role will lead interactions with global health...SuggestedFull time$217.6k - $256k
...Promotional Review Committee (PRC), providing regulatory guidance and oversight for promotional,... ...with Commercial, Marketing, Medical Affairs, Legal, Compliance, and Market Access... ...development, review, approval, and lifecycle management of promotional materials and programsand...SuggestedLocal area$200k - $300k
...Regulatory Affairs (Clinical/Nonclinical)SystImmune is a leading and well-funded clinical-stage biopharmaceutical company located in Redmond... ...meetings and associated briefing document preparationLead and manage queries and commitments with regulatory agencies, collaborate...- ...on‑site role located in East Brunswick, NJ, for a Director of Regulatory Affairs. The Director of Regulatory Affairs leads regulatory strategy... ..., annual reports, and other regulatory filings to FDA‑CVM Manage responses to FDA deficiency letters, information/amendment...Full time
$145.6k - $279.4k
...now or in the future. Job Description Leads and manages the preparation, review, and submission of regulatory applications, including product registrations, progress... ..., and/or medical devices. Represents Regulatory Affairs on research, development, and marketing project...Work at officeRemote workRelocation packageFlexible hours- ...485 certified. We are strengthening our U.S. -based quality management system and integrating global operations as we transition from... ...Position Summary: We are seeking an experienced Senior Regulatory Affairs Quality Systems Manager to lead FDA 510(k) and CLIA...Overseas
- ...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
- ...Job Description Job Title: EH&S Engineer (Manager to Director level) \n Location: Onsite, Cranbury & South Plainfield NJ \... ...requirements, hazardous waste management, chemical safety, and regulatory compliance. \n \n Responsibilities: \n (The responsibilities...Full timeLocal area
- ...Description Our Pharmaceutical client is seeking a Director Regulatory Affairs Chemistry Manufacturing & Controls (CMC) to guide global... ..., and ensure clear communication of risks to the executive management. Lead all RA-CMC operations through all phases of clinical...Work at office
- ...Description Our Pharmaceutical client seeks a Global Director Regulatory Affairs Strategy to guide global teams through the development and... ...with Health Authorities. Provide on project teams or management committees regulatory expertise/advice on requirements for pre...
- ...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
$189.7k - $237.1k
...Position Summary Join Acadia as the Director, Regulatory CMC and play a critical role in... ...development, marketing approvals, and lifecycle management across key regions including GCC, LATAM,... ...Manages the CMC regulatory affairs activities for marketed products and compounds...Work at officeLocal areaRemote workWorldwideNight shift3 days per week$212.5k - $250k
...dynamic and expanding mid-size company in the role of Director for Regulatory CMC directly reporting to Executive Director, Regulatory CMC.... ...skills. Position Summary With minimal direction the incumbent manages the global regulatory CMC activities except Asia for all...For contractorsLocal area- Description ~Develop, implement and manage the company’s compliance program for compliance with applicable laws and regulations relating to the sale of branded and generic pharmaceutical products. ~Managing the company’s compliance with state and federal law program...
- ...community programs, and local organizations. Partner with the Executive Director and leadership team to achieve occupancy goals. Manage leads, referrals, and follow-up activity using CRM tools. Monitor local market trends and identify opportunities to grow...Work at officeLocal area
- ...FDA quality regulations is a plus.Strong attention to detail and documentation accuracy.Ability to work independently and as part of a team in a fast-paced environment.Excellent time management and problem-solving skills.Proficiency in Microsoft Office (Word, Excel)....Work at office
$160.1k - $286k
...improvement, or a similarly rigorous analytical environment. Strong preference for candidates with experience at a leading strategy or management consulting firm, particularly in business diagnostics, commercial due diligence, corporate finance, performance improvement, or...Full timeWork at officeImmediate startRemote work- ...outpatient services, including psychiatric evaluations, medication management, individual and group therapy, intensive outpatient programs (... ...care, operational excellence, financial stability, and regulatory compliance. The COO works closely with the CEO and leadership...Shift work
$250k - $275k
...with a 5% employee contribution), and more. The C&S team is made up of educators, designers, researchers, strategists, project managers, and civic leaders. We value constant learning, belonging, gratitude, attentiveness, and a willingness to roll up our sleeves. Here...Remote workNight shift- ...highly motivated Compliance Analyst to support our AML/BSA and regulatory compliance program. This position offers an excellent... ...regulatory reporting, vendor oversight, and compliance project management. This role combines automated compliance systems with manual (...Work at officeRemote work
- ...Spend Your Time:*** Assisting audit teams with planning and testing of franchisees and licensees’ compliance, financial and brand management, with the contractual obligations for all contract compliance audits* Performing analysis of the franchisees and licensees’...Contract workWork at officeLocal area
$217.52k - $263.58k
...pharmacovigilance and REMS compliance programs, ensuring sustained regulatory compliance and quality excellence across global patient safety... ...to identify and mitigate risks Chair Safety Quality Management Forum and sponsor REMS Governance Forum for effective escalation...- ...programs and events for members at the Club. Additionally, you will manage and oversee the rollout of creative and innovative educational... ...of services; manage and monitor department budget; ensure regulatory and safety practices are adhered to; communicate and work closely...Work experience placementAfternoon shift
$150k - $180k
...still need to build a sound quote when a lane calls for one. • Systems and performance. Use the TMS, load boards, and carrier management platforms to optimize capacity and service. Own the KPIs that matter here: on-time pickup and delivery, carrier performance, cost...Full timeLive inLocal area- ...Job Description Supervise and assist in the conduct of regulatory studies performed. Responsibilities include: Supervise study... ...Data interpretation and report writing. Client liaison. Management Responsibilities: Overall, day-to-day laboratory operation...Full timeMonday to Friday
- ...innovation, and digital transformation. As a member of the executive leadership team, you will report to the CEO, drive risk management, privacy, and compliance programs, and establish governance, metrics, and incident response across cloud, networks, #J-18808-Ljbffr...
$80k - $90k
...support to our CEO and Executive Leadership Team. This role is ideal for someone who thrives in a fast-paced environment, enjoys managing priorities and bringing structure to complex initiatives, and takes pride in ensuring important details and commitments never fall...Work at office
Do you want to receive more vacancies?
Subscribe and receive similar vacancies to Regulatory Affairs Manager. Be the first to apply!




