Regulatory Affairs Manager (UK/EU)
Benjamin Moore Pell City
At Benjamin Moore, our success is attributable to the employees who dedicate their time and talents to the brand and exemplify our core values of openness, integrity, community, excellence, and safety. Benjamin Moore employees enjoy a competitive and well‑rounded benefits package, career development options, business resource groups, and opportunities to come together and connect with colleagues. We facilitate growth, development, and purpose for all through an inclusive and engaging workplace. Join us and be part of a brand that inspires creativity, innovation, and passion while supporting locally owned stores in 65 countries. Position Summary The Regulatory Affairs Manager reports to the Director of Regulatory Affairs & Sustainability. Manages the Regulatory Affairs Team, working on a complex and diverse set of notification/regulatory requirements across multiple global markets to ensure products are compliant with relevant regulations before release to market. The Regulatory Affairs Manager is responsible for managing all aspects of complex regulatory affairs projects, from product development to the strategic delivery of a global pipeline to multiple markets. Responsibilities Lead and manage registration/notification projects in accordance with the global regulatory frameworks Manage global new product evaluations for raw materials, paint, and resin products, with focus on Europe (EU/UK) Be the regulatory point of contact for Benjamin Moore's paint and resin EU/UK business. Assess any regulatory changes impacting the paint and resin to ensure that future developments and existing products compliance Participate in designated and applicable working groups/committees representing BM to shape regulatory‑driven topics in line with BM’s strategic vision, and ensure timely communication to relevant functions Working with the Director to help shape future policy, gather, disseminate & assess regulatory, competitive intelligence for paint and resin Build and conduct training and communication materials to key stakeholders Supervise compliant Labels and SDS's creation Respond to regulatory questions from international customers. Qualifications BS/MS in chemistry, biology, or related fields, such as biotechnology, toxicology, or the law. 5 plus years of experience in a regulatory‑related field. Understanding and expertise in conducting regulatory risk assessments. Minimum of 3 plus years of experience working with BPR, CLP, and REACH regulatory frameworks. Extensive expertise in European (EU and UK) chemical regulations, with a focus on the Biocidal Products Regulation (BPR), Classification, Labeling and Packaging (CLP) Regulations and Packaging & Packaging Waste. Ability to lead, motivate, and participate in diverse, multi‑functional teams and networks. Effective organization skills and ability to manage a team and complete multiple tasks to meet deadlines. Effective communicator with networking skills and the ability to develop and maintain interpersonal relationships through all levels of an organization. Demonstrated ability to interpret regulations, including BPR, CLP, REACH and PPW in EU and UK Previous experience with WERCS or similar regulatory software is desirable. #J-18808-Ljbffr Benjamin Moore
$109.9k - $179.3k
...diseases. We are seeking an AssociateManager to join our Regulatory Affairs Strategy (Oncology) team.The Associate Manager, Regulatory Affairs will report to the Global... ...with CROs in the management of ex-US/ex-EU CTAs towards clinical trial activations preferredHigh...SuggestedFull timeWorldwide- ...or related scientific discipline. 5-7 years of experience in regulatory affairs CMC in the pharmaceutical industry. Demonstrated expertise... ...EudraLex). Excellent communication, collaboration, and project management skills, with the ability to effectively interact with cross-...Suggested
$205k - $341.6k
...We are seeking a Director to join our Regulatory Affairs Strategy team.The Director, Regulatory... ...expert. This role also carries people management responsibility, including mentoring and... ...with CROs in the management of ex-US/ex-EU CTAs toward clinical trial activations....SuggestedFull timeWorldwideRelocation package$170k - $190k
...Shinyaku Co., Ltd. In Japan Summary: CMC Regulatory Affairs develops and executes CMC regulatory... ...with cross-functional stakeholders. Manage external CMC regulatory expert... ...requirements and guidance (e.g., ICH, FDA, EU), and proactively assess impacts and risks...SuggestedTemporary workFor contractorsWork at officeFlexible hours- We are seeking a Regulatory Affairs Manager to join our team to lead and broaden the impact of our ongoing regulatory affairs efforts across the United States. You will be responsible for analyzing, communicating, and advocating for a state and regional regulatory climate...SuggestedFull timeWork at officeLocal areaShift work
- ...procedures.This role supports global regulatory compliance while contributing... ...improvement of the Quality Management System. It is well suited for... ...in medical device regulatory affairs, with exposure to quality... ...820, QMSR, ISO 13485, MDD & EU MDR).Demonstrated experience...Full timeContract workWorldwide
- ...Reference25-04573 Seeking an experienced CMC Writer / Project Manager to support regulatory submissions and ensure timely, high-quality documentation... ...Skills: Experience with any of IND/NDA/BLA submissions and EU MAA/IMPD filings. Ability to interpret and apply regulatory...Work at office
$183.8k - $294.1k
...solutions that turn dreams into possibilities. Job Description Regulatory Affairs Associate Director, Globalization Responsible for... ...Units, Regions, Central RA, and other functions to influence, manage, and/or oversee global registration processes and programs and...Daily paidTemporary workWork at officeLocal areaRemote workWorldwideFlexible hoursShift work- ...opportunitiesPrepare high-impact strategy presentations, business cases, and investment memos for executive leadership and senior management; clearly articulate complex strategic concepts and provide data-driven recommendations, leveraging executive presence to...H1bLocal areaShift work
$157.2k - $256.6k
...in one of our US locations or in Uxbridge, UK (hybrid).Discover your role:Own accurate,... ...staff and communicate clearly with senior management and partners.This role requires:Pharmacy,... ...in pharma or biotech.Well-informed on FDA, EU, and ICH guidelines governing pharmacovigilance...Full timeWorldwide- Nathan Kline Institute (NKI) is seeking an IRB staff member to support the human research protection program. The role focuses on maintaining IRB files, processing protocol submissions, and coordinating IRB meetings under HRPP guidelines. The incumbent educates research...Remote job
$105k - $115k
...will be empowered to assist various communities with creativity and independence. We will also leverage your existing leadership, management, and customer service skills, and in turn we will give you the experience and information you'll need to be successful in the...Currently hiring- ...across the behavioral health and substance use disorder portfolio managed by the company. The position expands to include authorization... ...gaps Provide advisory support on HIPAA, audit response, regulatory inquiries, and Joint Commission / AHCA compliance posture Develop...Contract work
$113.15k - $270.02k
...standardized processes and grow with a team that is not afraid to push the status quo.KPMG is currently seeking a SALT Direct Tax Senior Manager, Shared Services to join our Delivery Center.Responsibilities:Work in our compliance center of excellence to support engagement...Work at officeLocal area- ...Participate in the development of the CMC regulatory strategy for small molecules. These... ...controls with supervision. Responsible for the management of CMC activities related to... ...development/commercial teams and Regulatory Affairs teams. Participate in global regulatory...
- .... If you're as passionate about your future as we are, join our team.KPMG is currently seeking a Senior Director, Data Portfolio Management to join our Digital Nexus organization. This is a hybrid work opportunity.ResponsibilitiesDefine and lead the enterprise-wide data...H1bLocal area
$229.24k
...team that inspires excellence, delivers meaningful impact, and empowers you to shape your own future. KPMG is currently seeking a Managing Director to join our Business Tax Services practice.Responsibilities:Play a key role in developing the Private Enterprise Tax...Private practiceLocal area$110k
Job DescriptionDevelop and conduct insightful financial, operational, and strategic analysis and present results to management.Identify and track applicable business drivers to highlight risks and opportunities. Conduct analysis of business units, portfolio segments, geographic...Work experience placement$85k - $115k
Balchem Corporation is seeking a Benefits Specialist based in Montvale, New Jersey. This role involves managing employee benefit programs, ensuring compliance with relevant laws, and acting as a point of contact for benefits inquiries. Ideal candidates will have a Bachelor...- Werfen is seeking a Training Program Manager for their Orangeburg site. In this role, you will oversee training compliance and manage programs through Learning Management Systems (LMS). Responsibilities include delivering training, maintaining training data, and collaborating...Work at office
$72k - $141k
...advancing key compliance programs, enhancing regulatory responsiveness, and facilitating... ...ResponsibilitiesEngage in the full lifecycle of law change management, including intake of legislative and... ...in insurance, compliance, regulatory affairs, or audit.Demonstrated ability to...Full timeWork experience placementWork at office- ...cross-border payments company, seeks a senior compliance leader to own BSA/AML and sanctions programs. The role reports to senior management and the board, coordinating with regulators and auditors and building a scalable compliance framework. Hybrid position in...
$145k - $160k
...leader. It offers a full spectrum of water, waste, and energy management services, including water and wastewater treatment, commercial... ...across North America.Job DescriptionPosition Purpose:The Manager, Regulatory Business - Utilities, under the general direction of the Sr....Flexible hours$92.82k - $109.2k
...knowledge of Advent applications preferred- General knowledge and understanding of portfolio accounting, U.S. GAAP and the investment management industry- Excellent verbal and written communication skills- Proven team-oriented, leadership and organizational skills- CPA or...Full timeWork at officeLocal area3 days per week- ...Local Government in Human Capital Advisory for our Consulting practice.Responsibilities:Ability to identify new clients, lead and manage existing client relationships, and deliver Human Capital and Workforce Transformation services within the State and Local Government...Work experience placementH1bLocal area
- ...ensuring alignment with overall business objectives and risk management priorities; lead and champion firm-wide process improvement and... ...identifying and implementing changes in response to legislative and regulatory developments; set standards and provide guidance for all...H1bLocal areaShift work
- ...collaborations with universities, CROs, and regional partnersBuild relationships with academic and scientific stakeholders across APACSupport regulatory activities (e.g., dossiers, regional compliance awareness)Partner with Marketing & Sales to develop science-based tools, training...Remote workWorldwide
$180k - $220k
...commercialization, product quality, customer confidence, and regulatory readiness across Balchems business segments.Commercial organization... ...governance of an ISO/IEC 17025-aligned analytical laboratory management system, including the change management program required to...Work at officeWorldwide$100k - $150k
...and state tax credit opportunities.Key Responsibilities:Lead and manage R&D Tax Credit studies for clients across a variety of... ...and other inquiries from taxing authorities.Monitor legislative, regulatory, judicial, and administrative developments affecting research tax...Full timeContract workWork at officeLocal area3 days per week$150k - $175k
...families everywhere. JOB SUMMARY: The Sr. Manager, Quality Assurance, is a key member of the Quality & Regulatory Affairs team responsible for ensuring the quality,... ...comply with ISO 13485, FDA 21 CFR Part 820, and EU MDR guidelines. Achieve QA operational objectives...Full timeContract workWork at officeRemote work
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