130 Regulatory Managers jobs in London
Regulatory Affairs Manager
Posted 1 day ago
Job Viewed
Job Description
Walker Cole are recruiting for a Regulatory Affairs Manager position for an early stage ATMP pharmaceutical business. This is an exciting opportunity for a junior professional to grow and develop within the ATMP space from a range of skills and experience within the team.
A Regulatory Manager will bring:
- Regulatory CMC experience at early-stage development in ATMP and/or biological products
- A drive and willingness to learn and grow within this space.
- Ability to work well within a team, cross functionally and independently
As a Regulatory Manager you will:
- Work within an expert team on Regulatory CMC
- Support in CMC gap analysis, write guidance document and IMAPs
- IMPD, IND submissions and pre-clinical activities.
Early-Stage // Development // Pre-clinical // Regulatory CMC // Regulatory Affairs // Biologics // ATMP // Advanced Therapy //
Regulatory Affairs Manager
Posted today
Job Viewed
Job Description
Walker Cole are recruiting for a Regulatory Affairs Manager position for an early stage ATMP pharmaceutical business. This is an exciting opportunity for a junior professional to grow and develop within the ATMP space from a range of skills and experience within the team.
A Regulatory Manager will bring:
- Regulatory CMC experience at early-stage development in ATMP and/or biological products
- A drive and willingness to learn and grow within this space.
- Ability to work well within a team, cross functionally and independently
As a Regulatory Manager you will:
- Work within an expert team on Regulatory CMC
- Support in CMC gap analysis, write guidance document and IMAPs
- IMPD, IND submissions and pre-clinical activities.
Early-Stage // Development // Pre-clinical // Regulatory CMC // Regulatory Affairs // Biologics // ATMP // Advanced Therapy //
Regulatory Affairs Manager - CMC
Posted 1 day ago
Job Viewed
Job Description
Hobson Prior is seeking a Regulatory Affairs Manager - CMC to join a dynamic team in the biotech industry. In this role, you will focus on regulatory strategies and submissions related to Chemistry, Manufacturing, and Controls (CMC). This is an exciting opportunity to contribute to pre-clinical and early-phase projects in a rapidly evolving therapeutic area.
Please note that to be considered for this role you must have the right to work in this location.
Responsibilities:
- Lead the preparation of regulatory documents, including clinical trial applications (CTA), investigational new drug (IND) submissions, and genetically modified organism (GMO) applications.
- Collaborate with various teams to ensure manufacturing and analytical processes meet regulatory standards.
- Provide strategic input on regulatory pathways for complex biologics or biotech products.
Key Skills and Requirements:
- Strong understanding of regulatory processes, particularly in the EU and US.
- Experience with biologics, with a preference for candidates familiar with cell and gene therapy.
- Ability to work effectively across teams and adapt to a fast-paced environment.
For more information, please contact Syem Mannan .
If you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists visit the 'Contact Us' page.
Hobson Prior is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Hobson Prior is acting as an Employment Agency in relation to this vacancy.
By submitting this application, you confirm that you've read and understood our privacy policy, which informs you how we process and safeguard your data -
Regulatory Affairs Manager - CMC
Posted today
Job Viewed
Job Description
Hobson Prior is seeking a Regulatory Affairs Manager - CMC to join a dynamic team in the biotech industry. In this role, you will focus on regulatory strategies and submissions related to Chemistry, Manufacturing, and Controls (CMC). This is an exciting opportunity to contribute to pre-clinical and early-phase projects in a rapidly evolving therapeutic area.
Please note that to be considered for this role you must have the right to work in this location.
Responsibilities:
- Lead the preparation of regulatory documents, including clinical trial applications (CTA), investigational new drug (IND) submissions, and genetically modified organism (GMO) applications.
- Collaborate with various teams to ensure manufacturing and analytical processes meet regulatory standards.
- Provide strategic input on regulatory pathways for complex biologics or biotech products.
Key Skills and Requirements:
- Strong understanding of regulatory processes, particularly in the EU and US.
- Experience with biologics, with a preference for candidates familiar with cell and gene therapy.
- Ability to work effectively across teams and adapt to a fast-paced environment.
For more information, please contact Syem Mannan .
If you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists visit the 'Contact Us' page.
Hobson Prior is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Hobson Prior is acting as an Employment Agency in relation to this vacancy.
By submitting this application, you confirm that you've read and understood our privacy policy, which informs you how we process and safeguard your data - -policy.
Remote Pharmaceutical Regulatory Affairs Manager
Posted 21 days ago
Job Viewed
Job Description
Regulatory Affairs Manager (12 Month FTC)
Posted 1 day ago
Job Viewed
Job Description
We are seeking an experienced Regulatory Affairs Manager to join on a 12-month fixed-term contract , supporting compliance and nutrition across multiple European markets. This is a senior role with broad cross-functional exposure, ideal for someone with strong regulatory expertise who thrives in a fast-paced international environment.
Key Responsibilities
- Act as a subject matter expert on European food regulations, labelling, and claims.
- Provide expert guidance on regulatory matters for existing, new, and reformulated products.
- Lead the regulatory review and approval of consumer labels in English and French, with potential oversight of additional European markets.
- Manage and resolve complex regulatory incidents , engaging with internal teams and external authorities.
- Monitor and interpret emerging legislation , shaping compliance strategies and contributing to industry discussions.
- Support cross-functional projects, including product development, reformulations, and marketing communications.
- Drive improvements in regulatory processes and systems, including the rollout of new labelling software.
- Manage and develop contractors, ensuring delivery of compliance-related activities.
About You
- Degree in Life Sciences required; Master’s preferred.
- 8–10+ years’ experience in regulatory affairs/nutrition with a strong focus on European markets.
- 5+ years’ experience leading teams preferred.
- Deep knowledge of European food regulations and labelling requirements.
- Fluent in English and French (additional European languages an advantage).
- Excellent communication and influencing skills, with proven ability to manage senior stakeholders.
- Skilled in Microsoft Office, Adobe, SAP-PLM, and product lifecycle management systems .
What’s on Offer
- A 12-month fixed-term contract with significant responsibility and visibility.
- The opportunity to work across multiple markets and regulatory environments.
- A chance to shape compliance processes and contribute to industry discussions at European level.
Regulatory Affairs Manager (12 Month FTC)
Posted today
Job Viewed
Job Description
We are seeking an experienced Regulatory Affairs Manager to join on a 12-month fixed-term contract , supporting compliance and nutrition across multiple European markets. This is a senior role with broad cross-functional exposure, ideal for someone with strong regulatory expertise who thrives in a fast-paced international environment.
Key Responsibilities
- Act as a subject matter expert on European food regulations, labelling, and claims.
- Provide expert guidance on regulatory matters for existing, new, and reformulated products.
- Lead the regulatory review and approval of consumer labels in English and French, with potential oversight of additional European markets.
- Manage and resolve complex regulatory incidents , engaging with internal teams and external authorities.
- Monitor and interpret emerging legislation , shaping compliance strategies and contributing to industry discussions.
- Support cross-functional projects, including product development, reformulations, and marketing communications.
- Drive improvements in regulatory processes and systems, including the rollout of new labelling software.
- Manage and develop contractors, ensuring delivery of compliance-related activities.
About You
- Degree in Life Sciences required; Master’s preferred.
- 8–10+ years’ experience in regulatory affairs/nutrition with a strong focus on European markets.
- 5+ years’ experience leading teams preferred.
- Deep knowledge of European food regulations and labelling requirements.
- Fluent in English and French (additional European languages an advantage).
- Excellent communication and influencing skills, with proven ability to manage senior stakeholders.
- Skilled in Microsoft Office, Adobe, SAP-PLM, and product lifecycle management systems .
What’s on Offer
- A 12-month fixed-term contract with significant responsibility and visibility.
- The opportunity to work across multiple markets and regulatory environments.
- A chance to shape compliance processes and contribute to industry discussions at European level.
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EU Regulatory Affairs Senior Manager - Oncology
Posted 20 days ago
Job Viewed
Job Description
If you feel like you're part of something bigger, it's because you are. At Amgen our shared mission-to serve patients-drives all that we do. It is key to our becoming one of the world's leading biotechnology companies. We are global collaborators who achieve together-researching, manufacturing and delivering ever-better products that reach over 10 million patients worldwide. It's time for a career you can be proud of. Join us.
**SENIOR REGULATORY AFFAIRS MANAGER**
**LIVE**
**What you will do**
In this vital role you will work to ensure that Amgen acquires and maintains all the required licenses in order to support clinical trials for investigational medicinal products as well as market commercially approved medicinal products.
Representing the EU region, you will be responsible for advising the GRT on regional considerations in developing strategy, and ensuring the regional needs are well defined and implemented in collaboration with relevant regional stakeholders.
+ Develop and execute regional regulatory product strategies, including precedence, risk management and contingency planning
+ Plan and manage regulatory submissions (e.g. clinical trial and marketing applications) for products within Amgen's portfolio in compliance with global filing plans and local regulatory requirements
+ Implement product related regulatory strategies, Regulatory Affairs processes and activity planning
+ Lead development of regional regulatory documents and meetings in accordance with GRT strategy
+ Provide regulatory direction on regional regulatory mechanisms to optimize product development (e.g. expediting FIH studies, Orphan Drug, Fast Track, compassionate use and paediatric plan)
+ Consistent with GRT strategy, advise on regulatory implications and requirements related to global clinical development plans and objectives
+ Lead Health Authority and Agency Interactions and document and communicate outcomes appropriately
**Be part of our team**
You would be joining the European Regulatory team, part of the Global Regulatory Affairs function in Europe. You would be responsible for leading the European regulatory strategies and submissions for development and marketed products from first in human clinical trials to marketing authorisation, and throughout the products lifecycle.
This team is leading the regulatory activities for established products and also development assets.
**WIN**
**What we expect of you**
We are all different, yet we all use our unique contributions to serve patients. What we seek in you as an experienced professional, are these qualifications and skills:
+ Degree educated in a scientific discipline
+ Extensive experience in regional regulatory environment
+ Proven track record of developing and executing regional regulatory strategy
+ In-depth understanding of the drug life cycle and development process from a regulatory perspective
+ In-depth understanding of the registration procedures in region for MA, post approval changes, extensions and renewals.
+ Ability to lead teams and work collaboratively in a dynamic environment
+ Proactive approach to problem solving
+ Ability to understand and communicate scientific/clinical information
+ Ability to anticipate regulatory agency expectations
+ Strong awareness of the needs of internal and external stakeholders, and the role of Regulatory Affairs in driving successful drug development
**THRIVE**
**What you can expect of us**
As we work to develop treatments that take care of others, so we work to care for our teammates' professional and personal growth and well-being.
+ Growth opportunities to learn and move up and across our global organization
+ Diverse and inclusive community of belonging, where teammates are empowered to bring ideas to the table and act
+ Generous Total Rewards Plan comprising health, finance and wealth, work/life balance, and career benefits
**LOCATION:** Ability to work flexibly from home with regular office work either from our Cambridge or Uxbridge next generation workspace.
The position can also be located in our Lisbon office.
**APPLY NOW**
**for a career that defies imagination**
In our quest to serve patients above all else, Amgen is the first to imagine, and the last to doubt. Join us.
**careers.amgen.com**
Amgen is an Equal Opportunity employer and will consider you without regard to your race, colour, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status.
We will ensure that individuals with disabilities are provided a reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request an accommodation.
Compliance and Regulatory Manager
Posted 1 day ago
Job Viewed
Job Description
ORGANISATIONAL CONTEXT & JOB PURPOSE
At INEOS Energy we produce and trade oil, gas, power and liquefied natural gas (LNG), both physical and financial. This is supported by our investments in low carbon technologies, which will help sustain our business through the energy transition. Direct examples of these areas are ‘Project Greensand’, our pioneering carbon storage project in the Danish North Sea, and our investment in HydrogenOne Capital Growth plc.
INEOS Energy Trading trades, moves and stores oil, gas, power and LNG, both from the INEOS Group’s own production and from third parties, and trades financial energy products. It is a rapidly growing, dynamic business within the INEOS Group.
The role will involve:
- assisting the Energy Trading business in reviewing the entirety of its compliance and regulatory policies and procedures
- enhancing them where necessary in order to ensure full compliance with all applicable laws and regulations and
- handling the business’ current compliance programme (as described below).
RESPONSIBILITIES & ACCOUNTABILITIES
The successful candidate will report to the Risk Director and will work very closely with the Head of Legal and Compliance, Trading Director, and other members of the Legal and Compliance team.
They will assist the business in upgrading its compliance and regulatory programme, including:
- being the initial point of contact for all Compliance & Regulatory issues. Providing support to the Head of Legal & Compliance on communications with regulators
- Regulations: ensuring compliance with all relevant regulations, including MiFID II, EMIR, REMIT, Dodd Frank, CFTC, exchange rules, licences and permitting (and, ideally, those ESG issues that are specifically relevant to the business, such as methane emissions regulations)
- Surveillance & monitoring: leading projects to implement a market surveillance tool and to improve the monitoring of communications media; handling market and communications surveillance for the business
- Risk assessment: providing and up-dating a comprehensive assessment of Compliance & Regulatory risks and mitigants
- Policies: ensuring that the business has a suite of appropriate Compliance policies and procedures
- Training: providing Compliance & Regulatory training to all staff, including on market abuse and competition law
- Ethics: working to ensure uniformly high ethical standards throughout the business
- Investigations: initial investigation of all compliance and ethical issues, including market abuse. Support to the Head of Legal & Compliance on more detailed investigations
SKILLS KNOWLEDGE & EXPERIENCE
Education/Experience
Experienced compliance and regulatory expert with hands-on experience in the commodity sector.
Skills & Knowledge
- In depth knowledge of the laws and regulations affecting trading, including REMIT, EMIR, MiFID II, Market Abuse Regulations, Dodd Frank, CFTC. competition law and sanctions issues
- Ability to make complex concepts clear and understandable.
Preferred Software Experience
Standard office systems (Word, SharePoint)
Behavioural skills
- High ethical standards
- Hands-on, practical approach to Compliance & Regulatory issues
- Positive, “can do”, solution-based attitude
- Strong communication skills, both written and oral, with the ability to deal with complex issues in a straight-forward way
- Organised, methodical, thoughtful
- Ability to work under pressure
WHAT WE OFFER
- Competitive salary + bonus + pension
- Flat structure being a key member of a small team
- On-site gym with an active internal sports department
- Wide range of staff discounts on INEOS products and partnerships.
- Flexible benefits including health, dental, car and bike scheme
Notice To Third Party Agencies:
INEOS does not accept unsolicited CVs from recruiters, employment agencies, or other staffing services. Unsolicited CV include any CV or hiring document sent to INEOS in the absence of a signed Service Agreement where INEOS has expressly requested recruitment/staffing services specific to the position at hand. Any unsolicited resumes, including those submitted to hiring managers or other business leaders, will become the property of INEOS and INEOS will have the right to hire that candidate without reservation - no fee or other compensation will be owed or paid to the recruiter, employment agency, or other staffing service.
Compliance and Regulatory Manager
Posted today
Job Viewed
Job Description
ORGANISATIONAL CONTEXT & JOB PURPOSE
At INEOS Energy we produce and trade oil, gas, power and liquefied natural gas (LNG), both physical and financial. This is supported by our investments in low carbon technologies, which will help sustain our business through the energy transition. Direct examples of these areas are ‘Project Greensand’, our pioneering carbon storage project in the Danish North Sea, and our investment in HydrogenOne Capital Growth plc.
INEOS Energy Trading trades, moves and stores oil, gas, power and LNG, both from the INEOS Group’s own production and from third parties, and trades financial energy products. It is a rapidly growing, dynamic business within the INEOS Group.
The role will involve:
- assisting the Energy Trading business in reviewing the entirety of its compliance and regulatory policies and procedures
- enhancing them where necessary in order to ensure full compliance with all applicable laws and regulations and
- handling the business’ current compliance programme (as described below).
RESPONSIBILITIES & ACCOUNTABILITIES
The successful candidate will report to the Risk Director and will work very closely with the Head of Legal and Compliance, Trading Director, and other members of the Legal and Compliance team.
They will assist the business in upgrading its compliance and regulatory programme, including:
- being the initial point of contact for all Compliance & Regulatory issues. Providing support to the Head of Legal & Compliance on communications with regulators
- Regulations: ensuring compliance with all relevant regulations, including MiFID II, EMIR, REMIT, Dodd Frank, CFTC, exchange rules, licences and permitting (and, ideally, those ESG issues that are specifically relevant to the business, such as methane emissions regulations)
- Surveillance & monitoring: leading projects to implement a market surveillance tool and to improve the monitoring of communications media; handling market and communications surveillance for the business
- Risk assessment: providing and up-dating a comprehensive assessment of Compliance & Regulatory risks and mitigants
- Policies: ensuring that the business has a suite of appropriate Compliance policies and procedures
- Training: providing Compliance & Regulatory training to all staff, including on market abuse and competition law
- Ethics: working to ensure uniformly high ethical standards throughout the business
- Investigations: initial investigation of all compliance and ethical issues, including market abuse. Support to the Head of Legal & Compliance on more detailed investigations
SKILLS KNOWLEDGE & EXPERIENCE
Education/Experience
Experienced compliance and regulatory expert with hands-on experience in the commodity sector.
Skills & Knowledge
- In depth knowledge of the laws and regulations affecting trading, including REMIT, EMIR, MiFID II, Market Abuse Regulations, Dodd Frank, CFTC. competition law and sanctions issues
- Ability to make complex concepts clear and understandable.
Preferred Software Experience
Standard office systems (Word, SharePoint)
Behavioural skills
- High ethical standards
- Hands-on, practical approach to Compliance & Regulatory issues
- Positive, “can do”, solution-based attitude
- Strong communication skills, both written and oral, with the ability to deal with complex issues in a straight-forward way
- Organised, methodical, thoughtful
- Ability to work under pressure
WHAT WE OFFER
- Competitive salary + bonus + pension
- Flat structure being a key member of a small team
- On-site gym with an active internal sports department
- Wide range of staff discounts on INEOS products and partnerships.
- Flexible benefits including health, dental, car and bike scheme
Notice To Third Party Agencies:
INEOS does not accept unsolicited CVs from recruiters, employment agencies, or other staffing services. Unsolicited CV include any CV or hiring document sent to INEOS in the absence of a signed Service Agreement where INEOS has expressly requested recruitment/staffing services specific to the position at hand. Any unsolicited resumes, including those submitted to hiring managers or other business leaders, will become the property of INEOS and INEOS will have the right to hire that candidate without reservation - no fee or other compensation will be owed or paid to the recruiter, employment agency, or other staffing service.