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Blackfield Associates are proud to be exclusively partnered with a speciality pharmaceutical client, who due to growth, are looking to hire a Regulatory Affairs Director to join their UK based team; to be the overall lead for the Regulatory function. Proven minimum 10 years of regulatory affairs ...

Admitted to the bar and in good stan.

Group Head of Regulatory Affairs. Group Head of Regulatory Affairs. This strategic leadership role is responsible for overseeing all regulatory compliance and affairs across the organisation's markets.

JD or equivalent degree, or equivalent practical experience.Admitted to the bar and in good standing or otherwise authorized to.

Also support the wider Regulatory Affairs team as required to secure necessary regulatory consents in support of business plans and activities, and establishing regulatory policy positions accounting for regulatory Best Practice. As a Regulatory Affairs Manager, this role provides a unique opport...

Bachelor's degree or equivalent practical experience.

They are seeking a Senior Regulatory Affairs Manager, experienced in biologic clinical trial applications across UK/EU and, US experience is a bonus. Support maintenance and approval of drug applications to the regulatory agencies throughout the whole lifecycle of the product. Keep up to date wit...

Come join us!The roleThe Director, Public Policy and Regulatory Affairs – Europe is responsible for systematically monitoring policy, legislative, regulatory, and judicial trends affecting our business model and strategy across our European markets, for mana

Please send a cover letter and CV for the attention of Amanda Isom, Regulatory Affairs Director, at info@bloomregulatory. Bloom Regulatory is a regulatory consultancy specialising in cosmetic product compliance and regulatory interpretation and advice. Working in the areas of cosmetics, food supp...

Parexel Consulting is seeking a talented and experienced CMC Regulatory Affairs Professional to join our team as a Regulatory Affairs Consultant. Preparing for and interacting with regulatory agencies during drug submissions, responding to inquiries, and participating in regulator

A regulatory expert with a minimum 10 years of experience of working in a technical/regulatory affairs role within an international position. They are seeking a highly skilled and experienced international regulatory expert to lead their team and navigate the complex international regulatory land...

The Lead, Licensing & Regulatory Affairs - EMEA develops and aligns licensing strategies with business and service availability priorities, manages complex regulatory projects dealing with satellite and spectrum regulations, and identifies potential regulatory risks that may impact Kuipers abili

Campden BRI support our members with global Regulatory Support, across the UK, EU and internationally, we are looking for a 12 month fixed term contract to support us. The structure of food and drink legislation varies significantly around the world – Our experienced team of regulatory experts ca...

ResponsibilitiesProvide centralized support across Regulatory Affairs Advisory teams on their execution of assessing, interpreting, and advising on compliance obligations and readiness efforts throughout the regulatory life-cycle, including in external engagem

The Lead, Licensing & Regulatory Affairs - EMEA develops and aligns licensing strategies with business and service availability priorities, manages complex regulatory projects dealing with satellite and spectrum regulations, and identifies potential regulatory risks that may impact Kuipers abili

Blackfield Associates are proud to be exclusively partnered with a speciality pharmaceutical client, who due to growth, are looking to hire a Regulatory Affairs Director to join their UK based team; to be the overall lead for the Regulatory function. To be considered for the role of Regulatory Af...

Why you?Basic Qualifications:We are looking for professionals with these required skills to achieve our goals:Bachelor’s degreeExperience in Regulatory Affairs within a pharmaceuti

Internal: Compliance Manager – UK Regulatory Affairs and Conduct, Group Head of Compliance, Global Compliance Teams, Risk Management and Second Line Assurance; Executive Management, Beazley Functions and Underwriting units. To provide technical advice and support on Lloyd’s, PRA and FCA regulato

An exciting opportunity for a Head of Regulatory Affairs to join this highly successful business that provides labelling, consumer information and regulatory advice. OPPORTUNITY HIGHLIGHTSFully remote roleFluent in English and at least one

Our client is seeking an experienced Regulatory Affairs Associate Director who will manage and oversee the regulatory activities that underpin the supply of unlicensed and pre-reimbursement medicines into the global market. Regulatory experience and experience in developing regulatory strategy. R...

Why you?Basic Qualifications:We are looking for professionals with these required skills to achieve our goals:Bachelors degreeExperience in Regulatory Affairs within a pharmaceutical organization&l

At least 3-5 years of experience in domestic and international regulatory affairs and quality assurance. This is a great opportunity for a Compliance Specialist with experience in label development, compliance management and regulatory affairs. Stay informed about regulatory changes and interpret...

The Regulatory Affairs Manager will assist in the local coordination and execution of regulatory submissions in compliance with corporate standards and national regulatory requirements, and of Regulatory Affairs processes and deliverables for the UK and Ireland. What youll need to succeed&

The Regulatory Affairs Manager will assist in the local coordination and execution of regulatory submissions in compliance with corporate standards and national regulatory requirements, and of Regulatory Affairs processes and deliverables for the UK and Ireland. In order to be considered for this...

The Regulatory Director may be the single point of contact on assigned asset(s), responsible for regional and global regulatory strategy(ies). Experience in Regulatory Affairs within a pharmaceutical organization. This goal has to be achieved both as a component of an overall global regulatory ap...

We seek a talented senior policy and regulatory affairs officer to work closely with the head of policy and the wider team to deliver FODO Group goals. The successful candidate will have experience in regulatory affairs, ideally in healthcare.

Parexel Consulting is seeking a talented and experienced CMC Regulatory Affairs Professional to join our team as a Regulatory Affairs Consultant. As the Regulatory Affairs Consultant, you will collaborate closely with a multinational pharmaceutical company, ensuring the effective

The Regulatory Affairs for European Power role supports our traders, brokers and originators in optimising business opportunities as well as representing Vitol in industry associations and with other institutions at national and international level, as relevant. Regulatory Affairs for European Po...

What youll doPolicy Monitoring, Analysis and Guidance: Monitor, analyse and communicate changes in global regulatory policies, and advise executive leadership on potential regulatory risks and opportunities, while driving initiatives

Accountable to GRL and Global Regulatory TA Head for development of appropriate regional and/or global regulatory strategy(ies) and for delivery according to plans. Experience in Regulatory Affairs within a pharmaceutical organization. This goal has to be achieved both as a component of an overal...

As Senior Director, Regulatory Affairs, EMEA Defense Lead, youll join an EMEA-based team addressing the highest and emerging risks pertaining to all aspects of our business in EMEA including our people, our products, our users, legislators and society, and our ecosystem. About the job<b

A Regulatory expert with a minimum of 10 years of experience in a technical/regulatory affairs role, or in a related field in one of the following markets: Germany, France, Spain, Netherlands or Belgium. An exciting opportunity for a Head of Regulatory Affairs to join this highly successful busin...

If you are a seasoned regulatory affairs professional with a passion for driving regulatory excellence in a fast-paced biotechnology environment, we encourage you to apply for this exciting opportunity. We are seeking a highly skilled and experienced Senior Manager of Regulatory Affairs to join o...

Group Head of Regulatory Affairs. Lead and develop a high-performing Regulatory Affairs team, embedding a culture of compliance and operational excellence. Extensive experience in regulatory affairs within the.

Inputs into Home Care Global Regulatory Affairs (RA) strategy. HC UK/I Regulatory Affairs Lead. PhD in Regulatory Toxicology (preferred), Chemistry, Toxicology, Biological Science, Environmental Science or equivalent.

Also support the wider Regulatory Affairs team as required to secure necessary regulatory consents in support of business plans and activities, and establishing regulatory policy positions accounting for regulatory Best Practice. As a Regulatory Affairs Manager, this role provides a unique opport...

Regulatory Affairs & Entity Corporate Governance Manager for North Europe and the Middle East. Head of Regulatory Affairs & Entity Corporate Governance. Own strategic projects related to corporate governance and regulatory compliance, engaging with local partners, regulators, law enforcement agen...

Provide centralized support across Regulatory Affairs Advisory teams on their execution of assessing, interpreting, and advising on compliance obligations and readiness efforts throughout the regulatory life-cycle, including in external engagements. Program Manager, Regulatory Affairs, Advisory a...

The focus of this role is to be on top of and ahead of regulatory updates and regulatory change. Regulatory Analysis, Regulatory Mapping and Identifying Gaps between the FCA handbook and the business. Have prior experience in regulatory affairs within financial services.

The Lead, Licensing & Regulatory Affairs - EMEA develops and aligns licensing strategies with business and service availability priorities, manages complex regulatory projects dealing with satellite and spectrum regulations, and identifies potential regulatory risks that may impact Kuiper's abili...

Tether is seeking an experienced and visionary Head of Regulatory Affairs to design and execute global regulatory strategies for our Tether Data business vertical. Expertise in preparing complex regulatory documents and other major regulatory submissions, including the preparation and execution o...

Regulatory Advocacy and Collaboration : participating in regulatory agency interactions, engaging with relevant regulatory authorities, industry bodies, and policymakers to shape the regulatory landscape for crypto-asset service providers, advocating for policies that promote innovation while ens...

The Lead, Licensing & Regulatory Affairs - EMEA develops and aligns licensing strategies with business and service availability priorities, manages complex regulatory projects dealing with satellite and spectrum regulations, and identifies potential regulatory risks that may impact Kuiper's abili...

Policy Monitoring, Analysis and Guidance : Monitor, analyse and communicate changes in global regulatory policies, and advise executive leadership on potential regulatory risks and opportunities, while driving initiatives to influence regulatory frameworks as well as monitoring for change across ...

We are hiring a talented Senior Regulatory Affairs Associate who will be responsible for the hands-on regulatory activities associated with maintaining the portfolio of branded products within the Perrigo UKIE business. Our ideal candidate should have a minimum of 3 years’ experience in Regulator...

Why you?Basic Qualifications: We are looking for professionals with these required skills to achieve our goals:Bachelor's degreeExperience in Regulatory Affairs within a pharmaceutical organizationExperience working with Global Health Authorities and submissions for Pharmaceutical productsPreferr...