Regulatory Partner Job at Douglas Scott (Bristol)

Staff Product Partnerships Manager

Mercury is building a whole stack of financial tools for startups. The Product P...

Location

United States , San Francisco; New York; Portland

Salary:

198700.00 - 276000.00 USD / Year

Mercury

Expiration Date

Until further notice

Requirements

8+ years of relevant experience in banking, fintech, or financial services, with deep familiarity working with regulated financial institutions
Experience managing or working closely with core banking providers, issuing banks, or other regulated financial infrastructure partners
Be a strong partnership leader who enjoys owning complex, high-stakes relationships
Be an excellent communicator and highly organized project manager, comfortable operating across many stakeholders
Consistently exercise empathy, especially in highly regulated and constrained environments
Have a strong product sense and interest in how financial infrastructure enables customer outcomes
Be an effective negotiator with experience navigating complex commercial and regulatory discussions
Be technically inclined or comfortable interfacing with engineering and compliance teams on complex systems
Stay calm and focused while working on multiple critical initiatives in parallel
Exercise creativity while operating within regulatory and operational constraints

Job Responsibility

Manage a portfolio of strategic core banking, card, and regulatory partnerships critical to Mercury’s banking infrastructure
Be the driving force behind building and maintaining Mercury’s core banking partner ecosystem in support of our charter ambitions
Serve as the internal expert on core banking systems, regulated financial institutions, and the broader banking infrastructure ecosystem
Work closely with Legal, Compliance, Risk, Product, Engineering, and Finance to negotiate contracts, manage partner performance, and support regulatory readiness
Lead new partner selection, due diligence, and onboarding for core banking and regulatory partnerships
Translate partner requirements, constraints, and regulatory considerations into actionable internal plans and timelines
Unblock internal teams wherever possible and advocate for Mercury’s roadmap while balancing regulatory and partner expectations
Clearly communicate Mercury’s compliance posture, regulatory obligations, and technical architecture to external partners

What we offer

base salary
equity (stock options)
benefits

Fulltime

Product Compliance Manager, Banking

Join us in building the future of finance. Our mission is to democratize finance...

Location

United States , Menlo Park, CA; New York, NY

Salary:

123000.00 - 145000.00 USD / Year

Robinhood

Expiration Date

Until further notice

Requirements

5+ years of experience in financial services compliance, with deep experience in banking and fintech environments
Hands-on experience working with bank partners and engaging with state and federal regulatory agencies
Strong knowledge of applicable regulatory frameworks, including Unfair, Deceptive, or Abusive Acts or Practices (UDAAP), the Electronic Fund Transfer Act (EFTA), the Truth in Savings Act (TISA), and money transmission laws
Demonstrated ability to design and scale compliance programs for consumer financial products in a high-growth, technology-driven environment
Ability to navigate ambiguity, apply sound judgment, and communicate clearly on complex regulatory and product issues
Alignment with Robinhood’s mission to expand access to the U.S. financial system

Job Responsibility

Scale and oversee a compliance program supporting Robinhood’s banking products, including money transmitter compliance, consumer protection requirements, and regulatory and bank partner reporting
Lead regulatory, partner, and internal audits related to banking products, including preparation, response coordination, and remediation tracking
Partner closely with product and engineering teams to support the design, launch, and iteration of new banking features while integrating compliance requirements early in development
Own, maintain, and continuously improve banking compliance policies, procedures, and controls to align with internal standards and external regulatory and partner expectations

What we offer

Performance-driven compensation with multipliers for outsized impact, bonus programs, equity ownership, and 401(k) matching
100% paid health insurance for employees with 90% coverage for dependents
Lifestyle wallet — a highly flexible benefits spending account for wellness, learning, and more
Employer-paid life & disability insurance, fertility benefits, and mental health benefits
Time off to recharge including company holidays, paid time off, sick time, parental leave, and more
Exceptional office experience with catered meals, events, and comfortable workspaces

Fulltime

Senior Regulatory Consultant - Regulatory Project/Program Manager

As part of Parexel Consulting, you will play a vital role in helping biopharmace...

Location

United States

Salary:

Not provided

Parexel

Expiration Date

Until further notice

Requirements

BA/BS degree in a scientific, engineering, or healthcare discipline required
advanced degree (MS, PharmD, PhD) and/or PMP certification strongly preferred
Minimum of 7 years of progressive experience in the pharmaceutical, biotechnology, or related life sciences industry, with at least 5 years in regulatory or regulatory program management
Proven ability to partner on regulatory strategy and lead execution across all stages of product development, including IND/BLA/MAA submissions, global registration, and post-marketing activities
Deep understanding of U.S. regulatory requirements with working knowledge of international (ex-U.S.) regulations and agency expectations
Demonstrated success managing complex regulatory deliverables across cross-functional teams within a matrixed organization, while maintaining alignment to strategic priorities
Hands-on experience with eCTD and a strong command of regulatory documentation, formatting, and submission strategy
Exceptional communication and influencing skills, with the ability to synthesize complex regulatory information and translate it into clear recommendations for senior leadership and global stakeholders
Strong judgment and agility in managing competing priorities, resource constraints, and evolving program needs with flexibility and strategic foresight
Demonstrated ability to leverage project management tools and best practices to enhance visibility, efficiency, cross-functional alignment, and meeting effectiveness across GRSTs and project teams

Job Responsibility

Partner strategically with Global Regulatory Leads to shape and execute forward-looking, globally aligned regulatory plans across all stages of development and post-marketing
Translate regulatory strategy into integrated, actionable plans with clear milestones, critical paths, risks, and opportunities to support effective planning and decision-making
Lead the execution of regulatory plans, ensuring alignment between day-to-day operations and broader strategic objectives across global programs
Identify and propose innovative regulatory pathways and planning scenarios that align with global regulatory expectations and business objectives
Collaborate closely with cross-functional teams and senior leadership to drive clarity, alignment, and accountability for regulatory deliverables, timelines, and interdependencies
Facilitate Global Regulatory Subteam (GRST) meetings and other routine and ad hoc project review forums, ensuring meetings are purpose-driven, well-structured, and focused on decision-making, risk mitigation, and regulatory execution
Apply project management best practices for meeting management and hygiene, including developing and distributing agendas in advance, defining objectives and discussion topics, maintaining action logs, documenting key decisions and next steps, tracking follow-up items to closure, and ensuring materials are stored and communicated appropriately
Partner with Global Regulatory Leads and cross-functional stakeholders to maintain effective GRST governance, meeting cadence, stakeholder alignment, and communication flow across global and regional teams
Anticipate and troubleshoot complex regulatory project and operational challenges, implementing scalable solutions that strengthen team effectiveness, process efficiency, and submission readiness
Prepare and deliver strategic dashboards, reports, and scenario plans to senior stakeholders, translating regulatory progress and risks into actionable business insights

What we offer

Flexibility of working remotely
Supportive and dynamic team
Challenging assignments
Mentorship from experienced regulatory professionals
Opportunities for career growth
Diverse and global client exposure
Learn from experts
Flexible work arrangements

Fulltime

Regulatory Specialist

At 2San, we are at the forefront of innovation in the global healthcare industry...

Location

United States , Norwood

Salary:

80000.00 USD / Year

2San

Expiration Date

Until further notice

Requirements

Proven regulatory affairs experience within the healthcare sector, with a focus on Class 2 and Class 3 Self-Test IVDs
Deep understanding of regulatory requirements and processes for the US market, including 510(k) management, FDA submissions, and compliance management
Experience with developing, implementing, and managing Quality Management Systems (QMS) in accordance with US and international standards, including familiarity with ISO 13485
Ability to develop and implement regulatory strategies that align with company objectives and product lifecycle
Strong analytical skills for assessing regulatory compliance, interpreting guidelines, and resolving complex issues
Excellent written and verbal communication skills for effective liaising with regulatory bodies, internal teams, and external partners
Proactive in identifying potential regulatory obstacles and developing effective solutions
Meticulous attention to detail with the capability to manage multiple projects and priorities simultaneously
Bachelor’s degree in a relevant scientific discipline (e.g., Biology, Chemistry, Biomedical Engineering) required
advanced degrees or certifications in regulatory affairs or quality assurance preferred

Job Responsibility

Monitoring and management of new and existing 510(k) entries to ensure all product listings are current and compliant with regulatory requirements
Preparing and submitting FDA applications for new product approvals and amendments for existing products, ensuring all submissions are accurate and meet regulatory standards
Maintaining the regulatory tracker to ensure all information is current and in-line with local requirements
Maintaining regular contact with manufacturers for products supplier in US. Ensuring that their conformity assessment is not due to lapse and ensuring that a plan is in place for updated certification. (IVDD to IVDR)
Regularly reviewing and updating the Quality Management System (QMS) to ensure it aligns with both US and international standards, including ISO 13485, and addressing any gaps or non-compliances
Overseeing Complaints Management and Post-Market Surveillance Activities, including the collection, analysis, and reporting of customer feedback and adverse events to regulatory bodies as required. Implementing corrective actions and ensuring continuous product quality and safety monitoring in compliance with regulatory requirements
Collaborating with product development teams to provide regulatory guidance and support from concept through to commercialization, ensuring regulatory considerations are integrated into product lifecycle management
Navigating regulatory pathways to secure product approval and market entry, including strategizing for efficient and compliant product launches
Applying strong analytical skills to assess regulatory compliance, interpret complex regulatory guidelines, and undertake risk assessments for regulatory strategies and submissions
Proactively identifying potential regulatory challenges and obstacles and working collaboratively with cross-functional teams to develop and implement effective solutions

Sr Associate Regulatory Affairs

The Local Regulatory Representative (Sr. Associate) is assigned to one or more A...

Location

South Korea , Seoul

Salary:

Not provided

Amgen

Expiration Date

Until further notice

Requirements

At least 5 years of directly related experience
Business-level proficiency in Korean and English is required
Knowledge of Regulatory principles
Working with policies, procedures and SOP’s
Comprehensive understanding of regulatory activities and how they impact other projects and/or processes
Understanding of drug development
Under general supervision interact with local health and regulatory authorities for routine matters
Demonstrate ability to work in teams
Ability to understand and communicate scientific/clinical information

Job Responsibility

Assist in aligning local regulatory requirements with Amgen’s corporate standards
Provide national/regional input to and execute regulatory strategies
Plan and manage local regulatory submissions
Ensure local labels are developed and maintained
Act as the point of contact with regulatory agencies
Plan and manage clinical trial applications through CRO
Manage CRO work invoice and participate in global network
Work as a point of contact and oversight for Global Regulatory Affairs & Strategy
Contributes for the filing plan
Executes the filing plan

Manager, Regulatory Policy and Stakeholder Engagement

Responsible for implementing strategic regulatory initiatives and developing and...

Location

United States , Westwood

Salary:

145090.00 - 161210.00 USD / Year

EVERSOURCE

Expiration Date

Until further notice

Requirements

Bachelor’s degree in a business or technical discipline or related experience
Minimum of ten (10) or more years of experience successfully building relationships, leading change, and managing complex projects
Utility industry experience preferred
Excellent interpersonal skills
Organizational skills to lead multiple projects
Experience with building key relationships (externally and internally) and building credibility with key influencers
Thorough understanding of the policy initiative Regulators support
Strong analytical skills including experience using both qualitative principals and quantitative analysis to develop regulatory policy
Sound business judgment
Strong written and verbal communication skills

Job Responsibility

Implement strategic regulatory initiatives
Develop and build key regulatory relationships
Work with business partners to ensure regulatory filings and external facing documents are in alignment with regulatory policy positioning
Build and maintain strong relationships with key regulatory stakeholders
Identify opportunities to interact with key stakeholders and communicate the Company’s key initiatives
Evaluate regulatory and industry trends
Develop regulatory positions and new regulatory opportunities
Communicate regulatory model concepts to leadership
Execute regulatory policy for major concepts and filings
Work with internal and external partners on regulatory proposals for emerging policy issues

What we offer

Competitive total rewards program
Potential incentive
Benefits programs

Fulltime

Business Information Security Officer

A senior individual contributor role serving as the cybersecurity liaison for HP...

Location

Ireland , Leixlip

Salary:

Not provided

Hewlett Packard Enterprise

Expiration Date

Until further notice

Requirements

12+ years of experience in cybersecurity, risk management, or related fields, with significant exposure to financial services regulatory environments
proven ability to partner with business executives and influence decision-making through clear articulation of cyber risk in business and regulatory terms
deep knowledge of cybersecurity frameworks and controls relevant to financial institutions (NIST, ISO 27001, DORA, SOX, GDPR, etc.)
experience engaging with financial regulators, auditors, and external examiners on cybersecurity compliance
strong understanding of incident response processes, with the ability to coordinate remediation and communication at the business unit level
exceptional communication, stakeholder management, and executive presence
bachelor’s degree required
advanced degree and/or certifications (e.g., CISM, CISSP, CRISC) preferred.

Job Responsibility

act as the primary cybersecurity liaison for HPEFS, partnering with executives to translate cyber risk into business and regulatory impact and enable informed leadership decisions
inform the HPEFS leadership about emerging cyber threat landscape to be proactive in protecting the business
drive cybersecurity strategies tailored to the regulatory environment for financial services, including but not limited to Central Bank of Ireland requirements, Digital Operational Resilience Act (DORA), SOX, GDPR (cyber-related obligations)
lead cyber risk assessments for products, services, and bank operations, ensuring controls meet both enterprise and banking regulatory expectations
serve as the on-point liaison during security incidents impacting HPEFS, coordinating with CDRM’s centralized incident response team and driving business-side remediation and communication
oversee vulnerability management for HPEFS assets, ensuring issues are tracked, prioritized, and remediated in alignment with regulatory timelines and enterprise standards
partner with the HPEFS IT leader to align on security priorities, infrastructure controls, and technology programs impacting financial services operations
support closure of audit, regulatory, and compliance findings through coordination of corrective action plans and, where appropriate, risk acceptance processes
monitor evolving regulatory requirements and industry trends, advising leadership on compliance gaps, risk exposure, and readiness for regulatory examinations
influence enterprise cybersecurity priorities by advocating for HPEFS needs within the broader CDRM strategy

What we offer

health and wellbeing benefits
personal and professional development programs
unconditional inclusion in the workplace.

Fulltime

Regulatory Compliance Engineer

This role has been designed as ‘’Onsite’ with an expectation that you will prima...

Location

United States , Roseville

Salary:

89400.00 - 206500.00 USD / Year

Hewlett Packard Enterprise

Expiration Date

Until further notice

Requirements

Must have 5-10 years of Regulatory compliance experience
Have a Bachelor’s or Master’s degree in electrical engineering
5-10 years of industry experience
Expert knowledge in EMI/EMC, Safety and Telecom standards/requirements for ITE/Telecom products
Proven track record managing global product certifications across development teams, test labs, suppliers, manufacturing, and OEM/ODM partners
Solid experience in acquiring global regulatory compliance approvals for new and released products
Experience working with Safety Agencies (UL, CSA, TUV) engineers early in the design phase to identify design constraints to achieve safety certification without surprises after the design freeze
Experience working with the relevant EMC Labs and various countries regulatory body such as FCC, IEC, CCC, EAC, KCC, Brazil Anatel, Taiwan BSMI, India TEC, EU etc…
Proven track record with performing or supporting the design and testing required to obtain Safety, EMC, Telecom, and similar certifications
Communicate regulatory strategy, testing required, approval schedule, estimated cost, key risks and concerns to the NPI program team

Job Responsibility

Leads the project team on internal and outsourced product development projects to design reliable, cost effective and high-quality EMC and safety compliance solutions for moderately to complex Networking products
Collaborates and communicates with management, internal, and outsourced development partners regarding design status, project progress, and issue resolution regarding regulatory compliance
Represents the electrical hardware team on all aspects of Global regulatory requirements in the product design phase
Provides regulatory compliance support to engineering development projects and existing product changes throughout the product life cycle
Interfaces with cross-functional teams consisting of engineering, operations, manufacturing, sourcing, quality, service, and marketing to assure ongoing products are compliant to global regulations
Solve complex Safety, EMC, Telecom test issues and challenges, including debugging/troubleshooting to recommend resolution

What we offer

Health & Wellbeing
Personal & Professional Development
Unconditional Inclusion

Fulltime

Regulatory Partner

Douglas Scott

Location:
United Kingdom , Bristol

Category:
Legal

Contract Type:
Employment contract

Salary:

Job Description:

Job Responsibility:

Requirements:

Nice to have:

Additional Information:

Job Posted:
June 13, 2025

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

Similar Jobs for Regulatory Partner

Staff Product Partnerships Manager

Product Compliance Manager, Banking

Senior Regulatory Consultant - Regulatory Project/Program Manager

Regulatory Specialist

Sr Associate Regulatory Affairs

Manager, Regulatory Policy and Stakeholder Engagement

Business Information Security Officer

Regulatory Compliance Engineer

Regulatory Partner

Douglas Scott

Location:United Kingdom , Bristol

Category:Legal

Contract Type:Employment contract

Salary:

Job Description:

Job Responsibility:

Requirements:

Nice to have:

Additional Information:

Job Posted:June 13, 2025

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

Similar Jobs for Regulatory Partner

Staff Product Partnerships Manager

Product Compliance Manager, Banking

Senior Regulatory Consultant - Regulatory Project/Program Manager

Regulatory Specialist

Sr Associate Regulatory Affairs

Manager, Regulatory Policy and Stakeholder Engagement

Business Information Security Officer

Regulatory Compliance Engineer

Location:
United Kingdom , Bristol

Category:
Legal

Contract Type:
Employment contract

Job Posted:
June 13, 2025