Senior Specialist Regulatory Affairs

4 months ago


London, United Kingdom MSD Full time

We are a research-driven biopharmaceutical company. Our mission is built on the simple premise that if we “follow the science” that great medicines can make a significant impact to our world. We believe that a research-driven enterprise dedicated to world-class science can succeed by inventing medicine and vaccine innovations that make a difference for patients across the globe.

An exciting opportunity has arisen in the UK Regulatory Affairs Department, for a** Senior Specialist** to join our expanding team. The team manages a broad portfolio of prescription medicines for the UK, largely across the vaccine, oncology and infectious disease therapeutic areas and this role is accountable for undertaking a variety of regulatory activities across a range of products for the UK market.

**Responsibilities**:

- Life-cycle maintenance of all aspects of the marketing authorisation’s registered particulars.
- Liaising and negotiating with the Medicines and Healthcare products Regulatory Agency
- Implementation and communication of marketing authorisation’s changes across stakeholder groups. Ensuring all compliance activities are correctly managed.
- Generation and maintenance of prescribing information, patient information leaflets and packaging components, including artwork management, and ensure regulatory compliance with legislation and company approval systems.
- Developing and maintaining a sound knowledge of European and UK regulatory legislation and guidelines to provide advice and expertise internally for matters related to our products.
- Advocates for therapeutic areas/local positions on regulatory issues and trends internally and externally contributing to a broader policy platform.
- Representation of Regulatory Affairs at cross functional meetings including product acquisitions and ad-hoc product issues.
- Utilizing and maintaining company compliance systems in relation to product portfolio and meeting compliance expectations.
- Working as a strong member of the UK regulatory team, contributing to departmental meetings, ad-hoc projects and issues.
- Maintaining a positive relationship with internal and external regulatory contacts.
- Utilising and maintaining company compliance systems in relation to product portfolio and meeting compliance expectations.
- Working as a strong member of the UK regulatory team, contributing to departmental meetings, ad-hoc projects and issues.

**Qualifications and Experience**:

- Solid and deep knowledge of Regulatory Affairs through working in a Regulatory Affairs related role in the pharmaceutical industry.
- Comprehension of the fast evolving EU and UK regulatory procedures and EU and UK Medicines Legislation.
- Exposure to regulatory submissions and working with a Regulatory Authority would be a strong advantage.
- Excellent verbal and written communication and interactive skills.
- Work on own initiative and take responsibility for managing the day to day regulatory activities for a portfolio of products.
- Work effectively within the Regulatory Affairs team and with other stakeholders to deliver on Company Objectives and Goals.
- Able to multitask and manage conflicting priorities with sound time-management skills.
- Able to demonstrate a genuine interest and knowledge of the regulatory environment and a desire to succeed in a Regulatory Affairs role in the pharmaceutical industry.
- Ability to identify compliance risks and escalate when necessary

Our Regulatory Affairs team bring new medical advancements to the world by facilitating communications and procedures that allow swift, organized compliance partnering with external regulatory agencies. We are on the leading-edge of healthcare breakthroughs that help provide new, reliable, and compliant medical products, practices and solutions to the world.

**THE COMPANY**

Our presence in the UK goes back a long way. For over 80 years, we’ve been researching, developing and supplying new medicines and vaccines that prevent and treat diseases that occur at every stage of life. Today we're one of the top five biopharmaceutical companies in the UK and employ over 2,000 people across five sites in Hertfordshire, Northumberland, Buckinghamshire, Edinburgh and London. We are officially certified by the Top Employer Institute and been awarded the exclusive Top Employer United Kingdom Certification.

**WHO WE ARE **

For more than a century, we have been inventing for life, bringing forward medicines and vaccines for many of the world's most challenging diseases. Today, our company continues to be at the forefront of research to deliver innovative health solutions and advance the prevention and treatment of diseases that threaten people and animals around the world.

**WHAT WE LOOK FOR **

Imagine getting up in the morning for a job as important as helping to save and improve lives around the world. Here, you have that opportunity. You can put your empathy, creativity, digital mastery, or scientific genius to work



  • London, Greater London, United Kingdom VRS Regulatory Full time

    Regulatory Affairs OpportunityA unique chance to launch your career in chemical regulatory affairs with VRS Regulatory, a specialist scientific recruiter.About the Role:Work under the guidance of an experienced regulatory manager to provide support for a diverse range of chemical products.Conduct a variety of activities, including SDS authoring, updates,...


  • London, Greater London, United Kingdom VRS Regulatory Full time

    Regulatory Affairs OpportunityA unique chance to launch your career in chemical regulatory affairs with VRS Regulatory, a specialist scientific recruiter.About the Role:Work under the guidance of an experienced regulatory manager to provide support for a diverse range of chemical products.Conduct a variety of activities, including SDS authoring, updates,...


  • London, Greater London, United Kingdom VRS Regulatory Full time

    Job DescriptionA rare opportunity for an aspiring regulatory affairs professional to join the regulatory team at a global chemical products business:Work under the supervision of an experienced regulatory managerProvide regulatory support to a wide range of chemical productsOngoing and comprehensive trainingAn excellent opportunity to start and establish...


  • London, Greater London, United Kingdom VRS Regulatory Full time

    Job DescriptionA rare opportunity for an aspiring regulatory affairs professional to join the regulatory team at a global chemical products business:Work under the supervision of an experienced regulatory managerProvide regulatory support to a wide range of chemical productsOngoing and comprehensive trainingAn excellent opportunity to start and establish...


  • London, Greater London, United Kingdom Lawton Senior Living Full time

    Job DescriptionJob Title: Regulatory Affairs DirectorJob Summary:We are seeking a highly experienced Regulatory Affairs Director to join our team at Lawton Senior Living. As a key member of our leadership team, you will be responsible for ensuring that our organization is in compliance with all relevant regulatory requirements and industry standards.Key...


  • London, Greater London, United Kingdom Lawton Senior Living Full time

    Job DescriptionJob Title: Regulatory Affairs DirectorJob Summary:We are seeking a highly experienced Regulatory Affairs Director to join our team at Lawton Senior Living. As a key member of our leadership team, you will be responsible for ensuring that our organization is in compliance with all relevant regulatory requirements and industry standards.Key...


  • London, Greater London, United Kingdom Bionical Emas Full time

    Job Title: Senior Regulatory Affairs SpecialistBionical Emas is a global Clinical Research Organization (CRO) dedicated to bringing life-changing medicines to patients worldwide. Our unique service combines Clinical Development, Clinical Trial Supply (CTS), and Early Access Programs (EAP) to deliver seamless support to our pharma and biotech clients.About...


  • London, Greater London, United Kingdom Bionical Emas Full time

    Job Title: Senior Regulatory Affairs SpecialistBionical Emas is a global Clinical Research Organization (CRO) dedicated to bringing life-changing medicines to patients worldwide. Our unique service combines Clinical Development, Clinical Trial Supply (CTS), and Early Access Programs (EAP) to deliver seamless support to our pharma and biotech clients.About...


  • London, Greater London, United Kingdom Hays Specialist Recruitment Limited Full time

    Senior Regulatory Affairs Manager Contract US and EUYou will be working as a Senior Regulatory Affairs Manager, responsible for leading regulatory submission strategies globally. This role involves advising on regulatory strategies for innovative medicines for global markets, with a focus on FDA and EMEA interactions.Key Responsibilities:Develop and...


  • London, Greater London, United Kingdom Hays Specialist Recruitment Limited Full time

    Senior Regulatory Affairs Manager Contract US and EUYou will be working as a Senior Regulatory Affairs Manager, responsible for leading regulatory submission strategies globally. This role involves advising on regulatory strategies for innovative medicines for global markets, with a focus on FDA and EMEA interactions.Key Responsibilities:Develop and...


  • London, Greater London, United Kingdom Senior Care Authority of Inland Empire, CA Full time

    About the RoleWe are seeking a highly skilled Regulatory Affairs Specialist to join our team at Senior Care Authority of Inland Empire, CA. As a key member of our Compliance Division, you will play a critical role in supporting our business area and providing compliance advice and support.Key ResponsibilitiesProvide expert advice on regulatory matters...


  • London, Greater London, United Kingdom Medicines and Healthcare Products Regulatory Agency Full time

    Job SummaryWe are seeking a highly skilled Regulatory Affairs Specialist to join our team at the Medicines and Healthcare Products Regulatory Agency. This is a challenging opportunity to work in a dynamic environment, contributing to the regulation of medicinal products and ensuring public health protection.About the RoleThe successful candidate will be...


  • London, Greater London, United Kingdom Medicines and Healthcare Products Regulatory Agency Full time

    Job SummaryWe are seeking a highly skilled Regulatory Affairs Specialist to join our team at the Medicines and Healthcare Products Regulatory Agency. This is a challenging opportunity to work in a dynamic environment, contributing to the regulation of medicinal products and ensuring public health protection.About the RoleThe successful candidate will be...


  • London, Greater London, United Kingdom Medicines and Healthcare Products Regulatory Agency Full time

    About the RoleWe are seeking a highly skilled Regulatory Affairs Specialist to join our team at the Medicines and Healthcare Products Regulatory Agency. As a key member of our Innovative Medicines Function, you will play a crucial role in assessing the pre-clinical aspects of marketing authorisation and clinical trial applications for medicinal products.Key...


  • London, Greater London, United Kingdom Medicines and Healthcare Products Regulatory Agency Full time

    About the RoleWe are seeking a highly skilled Regulatory Affairs Specialist to join our team at the Medicines and Healthcare Products Regulatory Agency. As a key member of our Innovative Medicines Function, you will play a crucial role in assessing the pre-clinical aspects of marketing authorisation and clinical trial applications for medicinal products.Key...


  • South West London, United Kingdom Harrington Recruitment Ltd Full time

    **The Role** The Regulatory Affairs Specialist will report to the Commercial Director. This is expected to be a hybrid role, 3 days per week working from home and 2 days based South-West London. The person should be located a commutable distance to the office.. Working together with colleagues in Germany, the Regulatory Affairs Specialist will be required...


  • London, Greater London, United Kingdom Hays Specialist Recruitment Limited Full time

    Job SummaryHays Specialist Recruitment Limited is seeking a highly experienced Regulatory Affairs Manager to lead our regulatory submission strategies globally. As a key member of our team, you will be responsible for advising on regulatory strategies for innovative medicines for global markets.About the RoleThis is an exciting opportunity for a seasoned...


  • London, Greater London, United Kingdom Hays Specialist Recruitment Limited Full time

    Job SummaryHays Specialist Recruitment Limited is seeking a highly experienced Regulatory Affairs Manager to lead our regulatory submission strategies globally. As a key member of our team, you will be responsible for advising on regulatory strategies for innovative medicines for global markets.About the RoleThis is an exciting opportunity for a seasoned...


  • London, Greater London, United Kingdom Campden BRI Full time

    About the RoleCampden BRI is seeking a highly skilled Senior Regulatory Affairs Specialist to join our dedicated Regulatory Affairs team. As a Senior Regulatory Affairs Specialist, you will play a key role in maintaining and extending our high level of awareness of current food legislation, related issues, and likely developments in the EU and...


  • London, Greater London, United Kingdom Campden BRI Full time

    About the RoleCampden BRI is seeking a highly skilled Senior Regulatory Affairs Specialist to join our dedicated Regulatory Affairs team. As a Senior Regulatory Affairs Specialist, you will play a key role in maintaining and extending our high level of awareness of current food legislation, related issues, and likely developments in the EU and...