CrawlJobs Logo

EU Regulatory Development Manager

barclays.co.uk Logo

barclays

Location Icon

Location:
Ireland , Dublin

Category Icon
Category:
Finance

Job Type Icon

Contract Type:
Not provided

Salary Icon

Salary:

Not provided
Save Job
Save Icon
Apply Position

Job Description:

Embark on a transformative journey as an EU Regulatory Development Manager. This is a technical regulatory role supporting Corporate Banking for the European businesses, Barclays Bank Ireland and Barclays International Payments legal entities. You will support the Corporate Bank to meet its product and conduct regulatory compliance risk, obligations and commitments through horizon scanning and leading and managing the Corporate Banking impact assessments across the European jurisdictions. You will produce detailed impact assessments of regulations that impact Corporate Banking end-to-end (all products, coverage, supporting functional areas) and provide regulatory thought leadership for Corporate Banking within Barclays Europe.

Job Responsibility:

  • To assess the integrity and effectiveness of the banks internal control framework to support the mitigation of risk and protection of the banks operational, financial, and reputational risk
  • Knowledge of business areas, products, processes and platforms to be able to assess risk
  • Collaboration with various stakeholders across the bank and business units to improve overall control effectiveness through detailed documentation of control assessments, procedures, and findings
  • Identification and investigation of potential weaknesses and issues within internal controls to promote continuous improvement and risk mitigation aligned to the bank’s control framework, prioritised by its severity to disrupt bank operations
  • Development of reports to communicate key findings from risk assessment including control weaknesses and recommendations to control owners, senior management, and other stakeholders
  • Execution of reviews to determine the effectiveness of the bank's internal controls framework aligned to established and evolving policies, regulation, and best practice
  • Implementation of adherence to the Barclays Controls Framework and set appropriate methodology of assessing controls against the Controls Framework

Requirements:

  • Proven experience in interpreting and applying pan-EU and/or European in-country regulatory developments
  • Demonstrable technical expertise across a broad range of regulatory subject matter relevant to Transaction Banking, Wholesale Lending, and UK & International Corporate Banking
  • Track record of conducting regulatory or technical analysis, including assessment of compliance obligations and control requirements
  • Experience in collaborating effectively with key stakeholders, including business, risk, compliance, and technology teams, to deliver regulatory outcomes and implement control requirements
  • Evidence of some commercial and technical understanding of Transaction Banking and Wholesale Lending products, as well as associated business activities across multiple jurisdictions

Nice to have:

  • Having a high-quality degree level education
  • Being creative and forward thinking, striving to improve and find solutions through effective innovation and project management
What we offer:
  • Modern workspaces, collaborative areas, and state-of-the-art meeting rooms
  • Facilities include wellness rooms, on-site cafeterias, fitness centers, and tech-equipped workstations
  • Supportive and inclusive culture and environment
  • Flexible working arrangements
  • Embrace mobility, exploring every part of our operations as you build your career

Additional Information:

Job Posted:
December 23, 2025

Employment Type:
Fulltime
Work Type:
Hybrid work
Icon
barclays - All Job Offers
Job Link Share:
Copy Link Icon
Facebook Icon Twitter Icon LinkedIn Icon

Looking for more opportunities? Search for other job offers that match your skills and interests.

Briefcase Icon

Similar Jobs for EU Regulatory Development Manager

New

Non-Pharma Global Regulatory Affairs Manager

The Global Regulatory Sciences-Legacy Products-Non-Pharma Manager manages regula...
Location
Location
Italy , Bologna; Milano; Pomezia
Salary
Salary:
Not provided
it.alfasigma.com Logo
Alfasigma
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Proven experience in Regulatory Affairs within the pharmaceutical or life sciences industry, preferably within the food supplements, medical devices, and cosmetics sectors
  • Hands-on experience with regulatory submission processes, especially within EU and/or RoW markets or similar relevant experiences
  • Demonstrated ability to coordinate projects or deliverables with complexity and limited supervision
  • Advanced degree in Life Sciences, Pharmacy, Chemistry, or a related field
  • Good knowledge of global regulatory frameworks including EU regulations for medical devices (MDR, MDD) and relevant legislation for food supplements and cosmetics
  • Strong organizational skills, attention to detail, and ability to manage priorities
  • Collaborative mindset and effective communication with team members and stakeholders
  • Ability to operate independently on clearly defined assignments
  • Proficiency in Microsoft Office Suite and regulatory submission/document management tools
  • Fluent in English, both written and spoken
Job Responsibility
Job Responsibility
  • Accountable for providing the necessary regulatory inputs in a cross-functional team for the development of new projects
  • Accountable for the execution and implementation of global regulatory strategies by managing day-to-day activities for assigned products
  • Manage multiple regulatory workstreams independently, including authoring, reviewing and coordinating documentation for regulatory submissions such as variations, renewals and geo-expansions
  • Provide and review regulatory assessments for change controls and product updates
  • Responsible for the preparation, review and collection of documentation for submission and maintenance of Technical File and PTD for the project assigned
  • Provide critical review of documentation supporting regulatory applications
  • Coordinate with local affiliates and global stakeholders to ensure submissions are aligned with timelines and business priorities
  • Contribute to the preparation and presentation of regulatory project updates in internal meetings and governance committees
  • Execute defined regulatory tasks within scope and deadlines under the guidance of the Head
  • Support other relevant assignments as directed by supervisor
What we offer
What we offer
  • Competitive salary
  • Comprehensive benefits
  • Extensive opportunities for professional growth and development
Read More
Arrow Right
New

Senior Manager, Regulatory Affairs & Quality Assurance, APAC

Provide strategic Regulatory Affairs and Quality leadership for all APAC markets...
Location
Location
Singapore
Salary
Salary:
Not provided
avanos.com Logo
Avanos
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Bachelor’s degree in a relevant scientific or technical discipline
  • 6-10 years of experience in the medical device industry
  • Proven leadership experience with a track record in managing teams and developing long-term strategic initiatives
  • Strong written and verbal communication skills
  • Experience with regional or international regulatory submissions preferred
  • Strong computer proficiency
  • Understanding of regulatory requirements across major APAC markets
  • Familiarity with mandatory Quality Management System requirements across APAC
  • General knowledge of US FDA regulations (21 CFR, FDA guidelines) and EU CE marking processes is an advantage
Job Responsibility
Job Responsibility
  • Provide strategic Regulatory Affairs and Quality leadership for all APAC markets where Avanos operates
  • Partner with global and regional stakeholders to ensure full compliance with regulatory requirements, support business objectives, and strengthen the RA/QA capability across the region
  • Serve as an active member of the Global Regulatory & Clinical Affairs, Global Quality, and APAC Leadership Teams
  • Provide Regulatory and Quality leadership across all APAC markets
  • Recruit, build, and develop in-country RA/QA teams
  • Advise APAC cross-functional teams and Global RA & Clinical Affairs and Global Quality functions on regional regulatory requirements
  • Oversee the preparation, submission, and lifecycle maintenance of product registrations across APAC
  • Maintain regulatory databases
  • Direct the development and maintenance of regulatory systems and processes
  • Develop APAC regulatory strategies
What we offer
What we offer
  • comprehensive and competitive range of benefits
  • health care benefits
  • retirement plans
  • work/life benefits
Read More
Arrow Right

Senior Regulatory Specialist

The Senior Regulatory Specialist is responsible for planning, managing, and impl...
Location
Location
United States , Burnsville
Salary
Salary:
100000.00 - 130000.00 USD / Year
imricor.com Logo
Imricor Medical Systems
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Bachelor of Science in a scientific discipline or equivalent education/ training
  • 5+ years’ Regulatory and/or Compliance-related experience in a regulated industry
  • Previous experience with US and EU medical device regulatory requirements including Quality Systems and clinical investigations standards
  • Experience with preparation, submission, and approval for medical devices is required
  • Strong communication skills, both verbal and written
  • Strong analytical and problem-solving skills, as well as a good background in the medical device development process
  • Demonstrated ability to effectively manage multiple projects and priorities
  • Skills in multiple computer-based tools and software such as Word, PowerPoint, Excel, and Adobe Acrobat
Job Responsibility
Job Responsibility
  • Develops domestic and international strategies for regulatory approval of company products
  • Coordinates, compiles, and submits U.S. and international regulatory filings for new and modified products, including PMAs, 510(k)s, IDEs, CE Marking submissions, and other country-specific product registrations
  • Develops and maintains positive relationships with regulatory body reviewers through oral and written communications regarding clarification and follow-up of submissions under review
  • Reviews product and manufacturing changes for compliance with applicable regulations and impact on regulatory filings
  • Represents RA on cross-functional product development, manufacturing, and clinical support teams and provides regulatory leadership and feedback throughout the product development cycle. Provides recommendations for how to overcome regulatory barriers
  • Provides technical reviews of supporting documentation for inclusion in regulatory filings
  • Supports Medical Device Reporting (MDRs) and Medical Device Vigilance Reporting
  • Represents RA on other cross-functional projects, which may include process changes and continuous improvement efforts
  • Meets defined goals and objectives through own initiatives, activities, and available resources with minimal supervision
  • Performs other related duties and responsibilities, as assigned
What we offer
What we offer
  • Medical
  • Dental
  • Vision
  • Health Savings Accounts
  • Health Care & Dependent Care Flexible Spending Accounts
  • Disability Benefits
  • Life Insurance
  • Retirement Benefits
  • Fulltime
Read More
Arrow Right
New

Non-Pharma Global Regulatory Affairs Specialist

The Global Regulatory Non-Pharma Specialist manages regulatory documentation and...
Location
Location
Italy , Bologna
Salary
Salary:
Not provided
it.alfasigma.com Logo
Alfasigma
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • At least 5 years’ experience in Regulatory Affairs preferably within the food supplements, medical devices, and cosmetics sectors
  • Exposure to regulatory operations or documentation in EU and/or RoW markets or similar experiences is preferred
  • Advance degree in Life Sciences, Pharmacy, Chemistry, or a related field
  • Relevant certifications in Regulatory Affairs are considered a plus
  • Good knowledge of EU regulations for medical devices (MDR, MDD) and relevant legislation for food supplements and cosmetics
  • Strong attention to detail, time management and organizational skills
  • Willingness to learn and ability to work effectively in a team-based environment
  • Strong communication and interpersonal skills
  • Proficiency in Microsoft Office Suite and familiarity with document management systems
  • Fluent in English, both written and spoken
Job Responsibility
Job Responsibility
  • Contributing in a cross-functional team to provide the necessary regulatory input for the development of new projects
  • Support regulatory strategies by providing impact assessments
  • Collaborate actively with the Research & Development team to integrate regulatory requirements during the design and development of assigned products
  • Prepare, organize and submit regulatory documentation for submission and maintenance of dossiers for the projects assigned
  • Coordinate with local affiliates and global stakeholders to ensure submissions are aligned with timelines and business priorities
  • Manage multiple tasks in a fast-paced environment while keeping on task and to the company’s quality standards
  • Contribute to the preparation of regulatory project updates in internal meeting and governance committee providing regulatory input and flagging risks
  • Assist colleagues with administrative tasks
  • Execute defined regulatory tasks within scope and deadlines under the guidance of the Head
  • Review and validate commercial artwork, packaging, and labeling in compliance with EU Regulations, ensuring timely product launches
What we offer
What we offer
  • Competitive salary
  • Comprehensive benefits
  • Extensive opportunities for professional growth and development
Read More
Arrow Right

Head of Public Policy (Benelux & EU)

As Head of Public Policy (Benelux & EU), you will report to the VP Northern Euro...
Location
Location
Belgium , Brussels
Salary
Salary:
Not provided
creandum.com Logo
Creandum
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • A Bachelor degree in Law, Political Science, Public Policy, Business, Economics, Communications or similar
  • Professional fluency in English and Dutch
  • Experience in public affairs within mobility, transport, tech or other policy-driven sectors
  • Strong understanding of the Benelux and EU political environment and experience influencing regulatory and political processes
  • Ability to use data and evidence in policy development and advocacy
  • Ability to draft regulatory positions, consultation responses and policymaker-facing arguments
  • Experience leading complex cross-functional work with local and central stakeholders
  • Experience managing direct reports and developing teams
Job Responsibility
Job Responsibility
  • Developing and implementing the Benelux and EU policy strategy in collaboration with the VP Northern Europe, the local team and other central stakeholders
  • Leading policy development work by outlining regulatory positions, interpreting new rules and producing clear material for EU and national engagement
  • Working with Analytics and Product teams to strengthen Voi’s evidence base and advocacy positions
  • Identifying, monitoring and preparing for tenders across the region, ensuring the right policy positioning
  • Engage proactively with city and regional authorities to shape upcoming mobility tenders and secure opportunities for participation
  • Collaborating with Product, Operations, Legal, PR and Tender team to align regulatory positions and support readiness for upcoming rules
  • Owning and developing senior political, technical and administrative relationships across the Benelux and within relevant EU institutions
  • Representing Voi in consultations, conferences and working groups, on European and national level, ensuring consistent and professional presentation of Voi’s positions
  • Maintaining oversight of compliance matters in the region and on European level, and preparing internal processes for regulatory change
  • Managing and mentoring the regional policy team, setting goals, supporting development and ensuring alignment with Voi’s strategic priorities
What we offer
What we offer
  • Get “skin in the game” through our employee stock options program and influence policy development in the Benelux and EU
  • Work with inspiring, motivated and fun colleagues towards a shared mission
  • Join the micromobility-revolution and be a part of creating sustainable cities made for living, free from noise and pollution
  • Fulltime
Read More
Arrow Right

Regulatory Policy VP

The Regulatory Policy VP will play a key role in overseeing regulatory complianc...
Location
Location
Ireland , Dublin
Salary
Salary:
80000.00 - 110000.00 EUR / Year
accaglobal.com Logo
ACCA
Expiration Date
December 26, 2025
Flip Icon
Requirements
Requirements
  • A strong background in accounting, finance, or a related field within a Capital Markets / Investment Bank
  • Ideally Accounting or Risk Qualified
  • Proven expertise in regulatory compliance and policy development
  • Exceptional analytical and problem-solving skills
  • Excellent communication abilities to liaise with both internal and external stakeholders
  • A proactive approach to monitoring and adapting to regulatory changes
  • The ability to work effectively in a fast-paced and professional environment in Dublin
  • Individuals specifically coming from an Investment Bank or Capital Markets business
Job Responsibility
Job Responsibility
  • Develop and maintain regulatory policies in line with industry standards and local requirements: crucially - ICAAP, ILAAP, RRP, EBA/ ECB EU Stress Tests
  • Advise senior management on regulatory developments and their impact on business strategies
  • Coordinate with compliance teams to ensure adherence to all relevant regulations
  • Prepare and present regulatory reports for internal and external stakeholders
  • Act as a point of contact for regulatory bodies and address inquiries or audits as required
  • Monitor changes in the regulatory landscape and assess their implications for the organisation
  • Collaborate with cross-functional teams to embed regulatory considerations into operational workflows
  • Provide training and updates to staff on regulatory policies and best practices
What we offer
What we offer
  • excellent co bens and competitive bonus
  • Opportunities for professional development within the financial services sector
  • A permanent position offering job stability and career progression
  • A collaborative and professional work environment in Dublin
  • Potential for additional benefits aligned with industry standards
  • Fulltime
!
Read More
Arrow Right
New

Senior Associate Data Management

The Senior Associate, Data Management, will help drive key business operation in...
Location
Location
India , Hyderabad
Salary
Salary:
Not provided
amgen.com Logo
Amgen
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Familiarity with Global Clinical Trial Applications, Marketing Authorizations, Regulations, and Regulatory Guidance
  • In depth understanding of the Veeva Vault system
  • Good written and verbal communication skills
  • Detail oriented
  • Independent time management and prioritization skills
  • Work efficiently with little support and minimal to no supervision
  • Ability to work well with others in demanding situations with a positive attitude demonstrating tact, diplomacy, and respect
  • Critical thinking skills
  • Appropriate software skills as required
  • Strong analytical and problem solving, communication and presentation skills
Job Responsibility
Job Responsibility
  • Responsible for maintaining data within the Regulatory Information Management (RIM) system
  • Create and archive clinical trial, marketing application submissions and health Authority correspondence within Amgen’s RIM system
  • Serve as a Data Management SME within cross-functional collaborative initiatives
  • Deliver the implementation of new processes within Veeva Vault, XeVMPD, IDMP and other key regulatory initiatives, ensuring alignment with global regulatory standards and business objectives
  • Provide support on creating, running and analysing reports for data streamline projects
  • Develop and deliver training materials and presentations to a global audience
  • Manage the protocol Amendment New Investigator (PANI) submission updates
  • Manage 1572 forms for FDA submission
  • Provide support within the global data management team on US Certificate of Pharmaceutical Product (CPP) and EU Certificate of Medicinal Product (CMP) during additional workload periods
  • Adhere to Amgen processes, policies, guidelines, SOPs and training documentations
What we offer
What we offer
  • Competitive and comprehensive Total Rewards Plans aligned with local industry standards
Read More
Arrow Right

Director of Regulatory Affairs

ILIA is looking for a Director of Regulatory Affairs to join the team in buildin...
Location
Location
United States , Laguna Beach; New York City
Salary
Salary:
160000.00 - 175000.00 USD / Year
iliabeauty.com Logo
ILIA Beauty
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Minimum Bachelor’s degree in a relevant field (e.g., Life Sciences, Chemistry, Cosmetic Science, Regulatory Affairs)
  • 10+ years of regulatory experience in the cosmetic or personal care industry, with at least 3 years in a managerial or leadership role
  • In-depth knowledge of U.S. and international cosmetic regulations (e.g., FDA, EU, Health Canada), safety assessment practices, and industry standards
  • Strong analytical and problem-solving skills, excellent written and verbal communication skills, and the ability to work collaboratively across departments, vendors and government agencies
  • Proven ability to lead and mentor a team of regulatory professionals, fostering a high-performance culture focused on compliance and innovation
  • Strong network within regulatory agencies and industry associations
  • Ability to work in a fast moving, fast changing environment
  • This position may require occasional travel to meet with regulatory agencies, attend industry conferences, or other related travel
Job Responsibility
Job Responsibility
  • Develop and implement a global regulatory strategy that aligns with business objectives while ensuring product compliance and safety (e.g. market expansion, short and long-term regulation updates, etc.)
  • Responsible for ensuring that all products comply with relevant regulations and standards (e.g., FDA, EU Cosmetic Regulation, etc.) throughout their lifecycle, from product development to marketing and distribution
  • Collaborate and communicate effectively with internal and external teams including but not limited to
  • product development, research and innovation, all marketing functions, and quality assurance, to ensure compliance with domestic and international regulations
  • Oversee the preparation and submission of regulatory documents, including ingredient notifications, safety assessments, and product registrations
  • Oversee post-market surveillance, adverse event reporting, and recall management
  • Collaborate with product development, marketing, quality assurance, and supply chain teams to provide regulatory advice and guidance during product formulation, testing, and labeling
  • Coordinate with product marketing, product development and testing facilities to create claims substantiation protocols and consumer perception questionnaires
  • Review product labels, marketing materials, and communications to ensure compliance with advertising regulations and truthful representation of product benefits
  • Contribute to the utilization & advancement of our product lifecycle management (PLM) tool or internal tools to manage global registrations, claims substantiation, and documentation workflows
What we offer
What we offer
  • Bonus Opportunity
  • Health Benefits - 100% employer-paid medical, dental & vision coverage
  • Flex Time Off - No cap on personal time off and paid company holidays
  • Seasonal Flex Days - Flexible scheduling to enjoy extra time under the sun during the Spring & Summer season
  • Parental Leave - Up to 18 weeks paid parental leave
  • 401(k) - Save for your future with a 401(k) with a company match
  • Flexibility & Wellness Stipends - Monthly stipends to support remote work & self-care
  • Hybrid Work Model - Find your flow, working from home or from one of our offices
  • ILIA Products - Quarterly stipend to replenish your favorite products and try new ones
  • Fulltime
Read More
Arrow Right
Welcome to CrawlJobs.com –
Your Global Job Discovery Platform
At CrawlJobs.com, we simplify finding your next career opportunity by bringing job listings directly to you from all corners of the web. Using cutting-edge AI and web-crawling technologies, we gather and curate job offers from various sources across the globe, ensuring you have access to the most up-to-date job listings in one place.
Jobs by Category
Art and Entertainment Jobs Banking Jobs Call Center Jobs Construction Jobs Consulting Jobs Customer Service Jobs Education Jobs Energy Jobs Finance Jobs Gastronomy Jobs Health and Beauty Jobs Hospitality and Tourism Jobs Human Resources Jobs Insurance Jobs IT - Administration Jobs IT - Software Development Jobs Legal Jobs Logistics Jobs Manufacturing Jobs Marketing, Digital Marketing, SEO, SEM Jobs Media Jobs Nursing Jobs Office Administration Jobs Pharmacy Jobs Physical Work Jobs Public Relations Jobs Public Sector Jobs Purchasing Jobs Quality Control Jobs Real Estate Jobs Research and Development Jobs Sales Jobs
Job Positions Jobs by Country
United States Jobs United Kingdom Jobs India Jobs Canada Jobs Australia Jobs Poland Jobs Ireland Jobs Germany Jobs
Company
Blog About Us Contact
Follow Us
Facebook
X (Twitter)
LinkedIn
Instagram
© 2025 CrawlJobs Ltd. All Rights Reserved
Terms & Conditions Privacy Policy