Head of Regulatory Affairs Job at BioLife Plasma Services (Shanghai)

Head of Regulatory Affairs

The Head of Regulatory Affairs manages a central team that connects regulatory i...

Location

United Kingdom

Salary:

Not provided

Campden BRI

Expiration Date

Until further notice

Requirements

Degree qualified in a relevant subject, with extensive experience in food law
Extensive experience in regulatory affairs, regulatory intelligence, policy interpretation, or an equivalent field, ideally within food, beverage, or other regulated sectors
Proven track record as a recognised expert in regulatory matters, built through sustained delivery, external engagement and peer or client recognition
Experience leading teams or functions, including people development, performance management and capability building
Demonstrated experience in consultancy or advisory settings, working directly with clients on regulatory, compliance or market‑access challenges
Experience proof reading and/or producing high‑quality, insight‑driven outputs, such as regulatory summaries, impact assessments, horizon scans, or technical briefings
Highly developed analytical, interpretive, and critical‑thinking skills, with the ability to synthesise large volumes of technical, legislative or policy material into accurate, actionable insights
Innovative problem‑solving skills, able to generate new ideas and translate them into workable solutions within a multidisciplinary environment
Excellent written and verbal communication skills, producing authoritative guidance, reports and recommendations tailored for technical, commercial, and senior‑leadership audiences
Confident presenter, capable of representing Campden BRI at external events, client forums, conferences, and technical platforms

Job Responsibility

Strategic Regulatory Leadership
Cross‑Organisational Collaboration & Solution Development
Financial & Operational Leadership
People Leadership & Capability Development
Thought Leadership & Market Differentiation
Client Relationship Management & Strategic Partnering

What we offer

Reward platform with employee discounts and rewards
25 days holiday + 8 bank holidays
Buy and sell holiday scheme
A generous work save pension scheme, with employee contributions matched by the company up to 10%
Culture focus around work/life balance (early finish Fridays)
Subsidised onsite restaurant

Fulltime

Head of Global Regulatory Affairs

Karo Healthcare, a dynamic and growing personal-care retail company, is all abou...

Location

Sweden , Stockholm

Salary:

Not provided

Life Science Talent

Expiration Date

Until further notice

Requirements

Advanced degree in Life Sciences, Pharmacy, Medicine, or a related field
15+ years of Regulatory Affairs experience, including leadership roles within consumer healthcare, pharmaceuticals, medical devices, or related industries
Strong pharmaceutical regulatory experience, complemented by exposure to medical devices and/or cosmetics
Proven track record of developing and executing regulatory strategies across multiple markets and regulatory frameworks
Experience leading international teams and managing through leaders in a multi-layered organization
Strong business acumen with the ability to balance regulatory compliance, commercial objectives, and growth opportunities
Experience partnering with senior stakeholders across commercial, scientific, and operational functions
A builder's mindset with a passion for developing organizations, improving processes, and driving change
Comfortable operating in a dynamic, growth-oriented environment where strategic thinking and hands-on execution go hand in hand
A collaborative, pragmatic, and solutions-oriented leader with strong influencing skills and executive presence

Job Responsibility

Define and execute Karo's global regulatory strategy across pharmaceuticals, medical devices, cosmetics, and other consumer healthcare categories
Act as a key member of the Scientific Affairs Leadership Team, working closely with leaders across Pharmaceutical Development, R&D, Medical & Clinical Operations, Patient Safety, and Quality Assurance
Ensure Regulatory Affairs is a strategic business partner that enables innovation, portfolio growth, market expansion, and speed-to-market
Translate complex regulatory requirements into business opportunities and competitive advantage
Lead and develop a global Regulatory Affairs organization through a team of experienced leaders, strengthening leadership capability and empowering greater ownership across the function
Drive continuous improvement of regulatory processes, governance, and ways of working to increase efficiency and remove bottlenecks
Provide strategic regulatory input throughout product development, commercialization, claims strategy, lifecycle management, and market launches
Ensure timely submissions, approvals, compliance, and lifecycle activities across global markets and regulatory frameworks
Partner closely with Commercial, Innovation, Medical, Quality, and Supply teams to balance compliance requirements with business ambitions
Represent Karo externally with regulatory authorities, notified bodies, industry associations, and strategic partners

What we offer

Opportunity to create, grow, and encourage
Apart from a competitive salary pack, there are lots of growth opportunities to meet your personal ambitions
Flexible schedule and life work balance
Responsibility for exciting and challenging projects that have a direct, visible impact on our customers and the industry
Very positive work environment in a young, international, and motivated team
Start-up spirit while being a part of the large international organization with strong values

Fulltime

Head of Global Regulatory Affairs

Karo Healthcare, a dynamic and growing personal-care retail company, is all abou...

Location

Denmark , Copenhagen

Salary:

Not provided

Life Science Talent

Expiration Date

Until further notice

Requirements

Advanced degree in Life Sciences, Pharmacy, Medicine, or a related field
15+ years of Regulatory Affairs experience, including leadership roles within consumer healthcare, pharmaceuticals, medical devices, or related industries
Strong pharmaceutical regulatory experience, complemented by exposure to medical devices and/or cosmetics
Proven track record of developing and executing regulatory strategies across multiple markets and regulatory frameworks
Experience leading international teams and managing through leaders in a multi-layered organization
Strong business acumen with the ability to balance regulatory compliance, commercial objectives, and growth opportunities
Experience partnering with senior stakeholders across commercial, scientific, and operational functions
A builder's mindset with a passion for developing organizations, improving processes, and driving change
Comfortable operating in a dynamic, growth-oriented environment where strategic thinking and hands-on execution go hand in hand
A collaborative, pragmatic, and solutions-oriented leader with strong influencing skills and executive presence

Job Responsibility

Define and execute Karo's global regulatory strategy across pharmaceuticals, medical devices, cosmetics, and other consumer healthcare categories
Act as a key member of the Scientific Affairs Leadership Team, working closely with leaders across Pharmaceutical Development, R&D, Medical & Clinical Operations, Patient Safety, and Quality Assurance
Ensure Regulatory Affairs is a strategic business partner that enables innovation, portfolio growth, market expansion, and speed-to-market
Translate complex regulatory requirements into business opportunities and competitive advantage
Lead and develop a global Regulatory Affairs organization through a team of experienced leaders, strengthening leadership capability and empowering greater ownership across the function
Drive continuous improvement of regulatory processes, governance, and ways of working to increase efficiency and remove bottlenecks
Provide strategic regulatory input throughout product development, commercialization, claims strategy, lifecycle management, and market launches
Ensure timely submissions, approvals, compliance, and lifecycle activities across global markets and regulatory frameworks
Partner closely with Commercial, Innovation, Medical, Quality, and Supply teams to balance compliance requirements with business ambitions
Represent Karo externally with regulatory authorities, notified bodies, industry associations, and strategic partners

What we offer

Opportunity to create, grow, and encourage
Apart from a competitive salary pack, there are lots of growth opportunities to meet your personal ambitions
Flexible schedule and life work balance
Responsibility for exciting and challenging projects that have a direct, visible impact on our customers and the industry
Very positive work environment in a young, international, and motivated team
Start-up spirit while being a part of the large international organization with strong values

Fulltime

Head of Global Regulatory Affairs

Karo Healthcare, a dynamic and growing personal-care retail company, is all abou...

Location

Norway , Oslo

Salary:

Not provided

Life Science Talent

Expiration Date

Until further notice

Requirements

Advanced degree in Life Sciences, Pharmacy, Medicine, or a related field
15+ years of Regulatory Affairs experience, including leadership roles within consumer healthcare, pharmaceuticals, medical devices, or related industries
Strong pharmaceutical regulatory experience, complemented by exposure to medical devices and/or cosmetics
Proven track record of developing and executing regulatory strategies across multiple markets and regulatory frameworks
Experience leading international teams and managing through leaders in a multi-layered organization
Strong business acumen with the ability to balance regulatory compliance, commercial objectives, and growth opportunities
Experience partnering with senior stakeholders across commercial, scientific, and operational functions
A builder's mindset with a passion for developing organizations, improving processes, and driving change
Comfortable operating in a dynamic, growth-oriented environment where strategic thinking and hands-on execution go hand in hand
A collaborative, pragmatic, and solutions-oriented leader with strong influencing skills and executive presence

Job Responsibility

Define and execute Karo's global regulatory strategy across pharmaceuticals, medical devices, cosmetics, and other consumer healthcare categories
Act as a key member of the Scientific Affairs Leadership Team, working closely with leaders across Pharmaceutical Development, R&D, Medical & Clinical Operations, Patient Safety, and Quality Assurance
Ensure Regulatory Affairs is a strategic business partner that enables innovation, portfolio growth, market expansion, and speed-to-market
Translate complex regulatory requirements into business opportunities and competitive advantage
Lead and develop a global Regulatory Affairs organization through a team of experienced leaders, strengthening leadership capability and empowering greater ownership across the function
Drive continuous improvement of regulatory processes, governance, and ways of working to increase efficiency and remove bottlenecks
Provide strategic regulatory input throughout product development, commercialization, claims strategy, lifecycle management, and market launches
Ensure timely submissions, approvals, compliance, and lifecycle activities across global markets and regulatory frameworks
Partner closely with Commercial, Innovation, Medical, Quality, and Supply teams to balance compliance requirements with business ambitions
Represent Karo externally with regulatory authorities, notified bodies, industry associations, and strategic partners

What we offer

Opportunity to create, grow, and encourage
Apart from a competitive salary pack, there are lots of growth opportunities to meet your personal ambitions
Flexible schedule and life work balance
Responsibility for exciting and challenging projects that have a direct, visible impact on our customers and the industry
Very positive work environment in a young, international, and motivated team
Start-up spirit while being a part of the large international organization with strong values

Fulltime

Head of Global Regulatory Affairs CMC

This position is responsible for defining and executing global regulatory strate...

Location

Italy , Bologna; Milan; Pomezia

Salary:

Not provided

Alfasigma

Expiration Date

Until further notice

Requirements

15+ years of experience in regulatory affairs with strong focus on CMC
Deep expertise in global CMC regulatory requirements (FDA, EMA, ICH guidelines)
Proven leadership of global teams and complex regulatory programs
Demonstrated success in major filings and global product approvals
Advanced degree in chemistry, pharmacy, chemical engineering, or related scientific discipline (PhD preferred)
Strategic regulatory leadership and decision-making
Deep CMC scientific and technical expertise
Strong understanding of pharmaceutical manufacturing processes
Health authority interactions and relationship management
Proven ability to be hands-on, agile and lead organizational efforts and innovation by example

Job Responsibility

Define and lead global regulatory CMC strategies and execution for development, registration, and post-approval lifecycle management, leveraging frameworks such as RELIANCE where appropriate
Ensure alignment of CMC regulatory approaches with overall product development and commercialization strategies, partnering cross-functionally to ensure aligned approach
Provide strategic input into critical development milestones (e.g., IND/CTA, BLA/NDA, MAA)
Oversee the development of high-quality CMC regulatory dossiers, including Module 3 content and supporting documentation, including rigor in CMC regulatory justifications, control strategies, comparability, and specifications
Ensure alignment with ICH guidelines and evolving regulatory science expectations, proactively communicating these and their impact for Alfasigma across the organization
Lead regulatory support for manufacturing changes, site transfers, scale-ups, and technology transfers
Serve as the senior regulatory CMC representative in interactions with global health authorities (e.g., FDA, EMA)
Establish global frameworks for CMC change management, ensuring compliance and minimizing regulatory risk
Drive efficient handling of complex changes (e.g., process improvements, new technologies, dual sourcing)
Ensure global alignment and consistency across markets

What we offer

competitive salary
comprehensive benefits
extensive opportunities for professional growth and development

Fulltime

Head of Policy & Regulatory Affairs

Strengthen and elevate Gigaclear's voice where it truly counts—with central Gove...

Location

United Kingdom , Abingdon

Salary:

80000.00 - 85000.00 GBP / Year

360 Resourcing Solutions

Expiration Date

Until further notice

Requirements

Deep telecoms sector expertise
Hands-on experience working with Ofcom
Established and respected network
Credibility to be listened to and relied upon as an expert and champion by industry decision-makers and influencers
Ability to spend a significant proportion of time in London and at Head Office in Oxfordshire

Job Responsibility

Strengthen and elevate Gigaclear's voice with central Government, regulator, and across influential industry forums
Lead Policy and Regulatory Affairs team
Be a high-profile champion for rural connectivity
Act as Gigaclear's authoritative voice while promoting and protecting strategic interests
Lead multiple high-impact campaigns and initiatives

What we offer

Bonus
Car Allowance
Generous employer pension (up to 8% matched contribution)
Income protection & life assurance
25 days holiday (plus bank holidays), holiday purchase scheme and Yay Days
Health cash plan, 24/7 remote GP access and Employee Assistance Programme including counselling & legal advice
Unlimited access to online training and development content via Learning Management System
Long service benefits and monthly employee recognition
Enhanced maternity and paternity provisions
Flexible working environment

Fulltime

Head of Government & Regulatory Affairs

GEICO is seeking a highly strategic, innovative, and experienced Head of Governm...

Location

United States , Chevy Chase; New York City

Salary:

266000.00 - 494000.00 USD / Year

Geico

Expiration Date

Until further notice

Requirements

Bachelor’s degree required
Juris Doctor (JD) strongly preferred
15+ years of government affairs experience in the insurance or financial services industry
Demonstrated leadership and team management experience
Proven ability to develop and execute complex strategies
Exceptional ability to analyze complex legislative and regulatory environments
Excellent written and verbal communication skills
Demonstrated success cultivating trusted relationships with policymakers, regulators, and industry leaders
Deep understanding of auto insurance laws, regulations, and related policy issues
Proven ability to build internal alignment, foster cross-functional collaboration, and lead enterprise initiatives

Job Responsibility

Build and maintain trusted relationships with legislators, regulators, government officials, and key policymakers
Develop and execute comprehensive government relations strategies at federal and state levels
Partner with GEICO’s executive leadership to align advocacy strategies with enterprise goals
Analyze proposed legislation and regulations, assess business impact, and develop data-driven advocacy positions
Represent GEICO before legislative bodies, regulatory agencies, and trade associations
Oversee GEICO’s Political Action Committee (PAC)
Oversee engagement with insurance departments and regulators across all jurisdictions
Partner with Legal to assess and interpret new or evolving laws, rules, regulations
Lead, mentor, and develop a high-performing team
Collaborate with internal stakeholders and external partners

What we offer

Comprehensive Total Rewards program
401K savings plan vested from day one with a 6% match
Performance and recognition-based incentives
Tuition assistance
Access to mental healthcare
Fertility and adoption assistance
GEICO Flex program offering the ability to work remotely for up to four weeks per year

Fulltime

Head of Global Regulatory Affairs, CMC Small Molecule

Join the engine of Sanofi’s mission — where deep immunoscience meets bold, AI-po...

Location

United States , Morristown

Salary:

232500.00 - 335833.33 USD / Year

Sanofi

Expiration Date

Until further notice

Requirements

Minimum 10-15 years of direct Regulatory CMC experience preferred
Demonstrated progression in regulatory affairs roles and successful regulatory authority interactions
Global Leadership experience with a mid-size/large Regulatory CMC organization
Strong knowledge of key Agency/Industry thinking, trends and regulations / guidelines
Bachelor's degree required
Advanced degree (Masters, PhD) in a science or health field (i.e., Analytical, Chemistry, Pharmacy, Biological / Biotechnology Sciences, etc.), or equivalent is highly desirable
Demonstrated excellent communication and influencing skills internally and externally
Demonstrated ability to assess regulatory risks, identify opportunities, and develop pragmatic solutions that align with business objectives
Experience building and maintaining effective partnerships across functions and with external stakeholders, including health authorities
20% travel expected, domestic and international

Job Responsibility

Provides Leadership to their group and is accountable for organizational design, people development, resource allocation, and metrics
Oversees the development of CMC regulatory strategy and regulatory risk assessments for all development projects and marketed products
Assures that positive and collaborative relationships are developed with CMC and Device teams
Oversees strategic negotiations with worldwide Regulatory Agencies, including directly with FDA and EMA
Oversees the preparation review and approval of Regulatory CMC submissions
Provides a vision and leadership for Policy and Regulation to assure that appropriate Sanofi representation in external activities is achieved

What we offer

High-quality healthcare, prevention and wellness programs
At least 14 weeks’ gender-neutral parental leave

Fulltime

Select Country

Head of Regulatory Affairs

Job Description

Job Responsibility

Requirements

Nice to have

Looking for more opportunities?

Head of Regulatory Affairs

Head of Regulatory Affairs

Head of Global Regulatory Affairs

Head of Global Regulatory Affairs

Head of Global Regulatory Affairs

Head of Global Regulatory Affairs CMC

Head of Policy & Regulatory Affairs

Head of Government & Regulatory Affairs

Head of Global Regulatory Affairs, CMC Small Molecule

Our AI answers in your language