Current jobs related to Senior Regulatory Affairs Associate - United Kingdom - Bionical Emas


  • United Kingdom VRS Regulatory Full time

    An opportunity to join the Regulatory Affairs team at an R&D focussed global PPP company. You will: Manage a portfolio of plant protection products in specific geographical territories Develop regulatory strategy Become the subject matter expert on the regulations/guidelines in your territory. As a regulatory Specialist, you will develop regulatory...


  • United Kingdom VRS Regulatory Full time

    An opportunity to join the Regulatory Affairs team at an R&D focussed global PPP company. You will:Manage a portfolio of plant protection products in specific geographical territoriesDevelop regulatory strategy Become the subject matter expert on the regulations/guidelines in your territory. As a regulatory Specialist, you will develop regulatory strategy...


  • United Kingdom VRS Regulatory Full time

    An opportunity to join the Regulatory Affairs team at an R&D focussed global PPP company. You will:Manage a portfolio of plant protection products in specific geographical territoriesDevelop regulatory strategy Become the subject matter expert on the regulations/guidelines in your territory. As a regulatory Specialist, you will develop regulatory strategy...


  • United Kingdom VRS Regulatory Full time

    Exciting opportunity to join the regulatory affairs team at an established and highly reputable chemical regulatory science consultancy. This is expansion to cover an increasing workload. The role is delivery focussed with no commercial or business development aspects. We are looking for a regulatory person for a purely regulatory delivery role. This role...


  • United Kingdom VRS Regulatory Full time

    Exciting opportunity to join the regulatory affairs team at an established and highly reputable chemical regulatory science consultancy. This is expansion to cover an increasing workload. The role is delivery focussed with no commercial or business development aspects. We are looking for a regulatory person for a purely regulatory delivery role. This role...


  • United Kingdom VRS Regulatory Full time

    Exciting opportunity to join the regulatory affairs team at an established and highly reputable chemical regulatory science consultancy. This is expansion to cover an increasing workload. The role is delivery focussed with no commercial or business development aspects. We are looking for a regulatory person for a purely regulatory delivery role. This role...


  • United Kingdom Dechra Pharmaceuticals Limited Full time

    Dechra are a growing, global specialist within the world of veterinary pharmaceuticals. Our expertise is in the development, manufacture, marketing and sales of high quality products exclusively for veterinarians worldwide. From manufacturing to marketing, ( D )edication, ( E )njoyment, ( C )ourage, ( H )onesty, ( R )elationships and ( A )mbition are at...


  • United Kingdom Dechra Pharmaceuticals Limited Full time

    Summary Thanks for checking out our vacancy, we're delighted you want to learn more about Dechra. Dechra are a growing, global specialist within the world of veterinary pharmaceuticals. Our expertise is in the development, manufacture, marketing and sales of high quality products exclusively for veterinarians worldwide. Here at Dechra, our values are...


  • United Kingdom VRS Regulatory Full time

    A rare opportunity for an aspiring regulatory affairs officer 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 training. An excellent opportunity to start and establish your career in...


  • United Kingdom Regeneron Ireland DAC Full time £12,000

    Job Title: Regulatory Affairs ManagerRegeneron Ireland DAC is seeking a highly skilled Regulatory Affairs Manager to support our CMC development activities from a regulatory standpoint. The successful candidate will participate in cross-functional meetings, identify regulatory issues, and suggest strategies to mitigate risks.Key Responsibilities:Review...


  • United Kingdom Regeneron Ireland DAC Full time £12,000

    Job Title: Regulatory Affairs ManagerRegeneron Ireland DAC is seeking a highly skilled Regulatory Affairs Manager to support our CMC development activities from a regulatory standpoint. The successful candidate will participate in cross-functional meetings, identify regulatory issues, and suggest strategies to mitigate risks.Key Responsibilities:Review...


  • United Kingdom Regeneron Ireland DAC Full time £12,000

    Job Title: Regulatory Affairs ManagerRegeneron Ireland DAC is seeking a highly skilled Regulatory Affairs Manager to support the development and approval of gene therapies.Key Responsibilities:Participate in cross-functional meetings to discuss program-specific regulatory strategies.Identify and mitigate CMC regulatory risks.Review regulatory filing...


  • United Kingdom Regeneron Ireland DAC Full time £12,000

    Job Title: Regulatory Affairs ManagerRegeneron Ireland DAC is seeking a highly skilled Regulatory Affairs Manager to support the development and approval of gene therapies.Key Responsibilities:Participate in cross-functional meetings to discuss program-specific regulatory strategies.Identify and mitigate CMC regulatory risks.Review regulatory filing...


  • United Kingdom Reed Specialist Recruitment Ltd Full time

    Head of Regulatory Affairs (Healthcare) Location: North-West, UK Full time & permanent position Onsite 3-4 days per week Reed Scientific are working with a global healthcare provider based in the North West of the UK, and are currently seeking an experienced Regulatory Affairs Manager to oversee and manage the regulatory affairs team. Main...


  • United Kingdom Regeneron Ireland DAC Full time £12,000

    Job Title: Associate Director, Regulatory AffairsRegeneron Ireland DAC is seeking an experienced Associate Director, Regulatory Affairs to join our team in Dublin or Amsterdam. This role will be responsible for supporting development activities and developing teams in the area of cardiovascular, metabolic, and allergic diseases.Key Responsibilities:Lead and...


  • United Kingdom Regeneron Ireland DAC Full time £12,000

    Job Title: Associate Director, Regulatory AffairsRegeneron Ireland DAC is seeking an experienced Associate Director, Regulatory Affairs to join our team in Dublin or Amsterdam. This role will be responsible for supporting development activities and developing teams in the area of cardiovascular, metabolic, and allergic diseases.Key Responsibilities:Lead and...


  • United Kingdom Life Sciences Recruitment Full time

    We’re looking for an experienced Senior Regulatory Consultant to join my client. The ideal candidate will have deep expertise in regulatory affairs for medical devices and digital health, with a focus on FDA and EU MDR, and experience managing submissions for Software as a Medical Device (SaMD). Act as a regulatory expert on FDA, MDR, and other...


  • United Kingdom Reed Engineering Full time

    Head of Regulatory Affairs (Healthcare) Location: North-West, UK Full time & permanent position Onsite 3-4 days per week Reed Scientific are working with a global healthcare provider based in the North West of the UK, and are currently seeking an experienced Regulatory Affairs Manager to oversee and manage the regulatory affairs team. Main...


  • United Kingdom Regeneron Ireland DAC Full time £12,000

    Job Title: Senior Reporting ManagerRegeneron Ireland DAC is seeking a highly skilled Senior Reporting Manager to join our team in Dublin or Amsterdam. As a key member of our EU Regulatory Affairs team, you will play a critical role in ensuring the company's compliance with emerging EU legislation and processes.Key Responsibilities:Lead and develop EU...


  • United Kingdom Regeneron Ireland DAC Full time £12,000

    Job Title: Senior Reporting ManagerRegeneron Ireland DAC is seeking a highly skilled Senior Reporting Manager to join our team in Dublin or Amsterdam. As a key member of our EU Regulatory Affairs team, you will play a critical role in ensuring the company's compliance with emerging EU legislation and processes.Key Responsibilities:Lead and develop EU...

Senior Regulatory Affairs Associate

2 months ago


United Kingdom Bionical Emas Full time

A Career with Purpose


Bionical Emas is a global Clinical Research Organization (CRO) bringing life-changing medicines to patients around the world. We combine Clinical Development, Clinical Trial Supply (CTS) and Early Access Programs (EAP) to deliver a unique, seamless service to our pharma and biotech clients.

At Bionical Emas, you will have the chance to develop your career while working with an outstanding team of people. Our shared values create a unique culture that guides our actions and defines who we are. You will be a part of a welcoming, flexible, and supportive culture that values trust and belonging. We believe that creating opportunities for our people to develop their skills is crucial to our growth and success. If you are inspired by changing the lives of patients all over the world, we’d love to hear from you.


About the Role


We are looking for a Senior Reg Affairs Associate to join our EAP team on a fixed term contract basis. This individual will work to deliver strategic and operational regulatory support and expertise to the Regulatory team and clients to ensure efficient and compliant set-up, maintenance and close-out of projects.


What will your job look like?

  • Manage day-to-day regulatory affairs activities to ensure compliance with regulatory obligations and requests
  • With support from a senior regulatory team member, be the client point of contact for regulatory activities for assigned Early Access Programs and attend regular client calls to provide regulatory updates, as required
  • Provide an initial assessment for feasibility reviews or regulatory questions as required, with support from a senior regulatory team member
  • Develop Regulatory Strategy Reports and/ or regulatory plans at the start of each project
  • Manage and maintain trackers of regulatory activities relating to set-up, maintenance and close-out of projects
  • Develop key regulatory documents for regulatory submissions, including performing regulatory review of protocols and Informed Consent Forms
  • Prepare, collate and submit packages for regulatory submissions in line with local requirements, with support from a senior regulatory team member
  • Support with the development and maintenance of the regulatory database of global regulations and guidelines
  • Work closely with wider Bionical Emas Regulatory department to share learnings and to provide Regulatory expertise as required
  • Develop own external regulatory network relating to Regulatory Affairs for the purpose of regulatory intelligence and continuous professional development
  • Perform and manage administration of regulatory release of shipments


What will you need to succeed?

  • Bachelor’s degree in a healthcare/science-related subject preferred
  • Previous experience in regulatory affairs field within the pharmaceutical or clinical research organization (CRO) environment
  • Previous experience within EAP or compassionate use would be advantageous


What will you get in return?

We want you to do your best work We care about our people’s well-being, their personal development and providing a true work-life balance. Our benefits are aligned with our culture and values and are intended to maximize your experience working for us. Here are some of the benefits you can expect from working for Bionical Emas.

  • 25 days of vacation
  • Vacation days purchasing scheme
  • 1 extra vacation day per each 3 years of service
  • Discretionary Annual Bonus
  • Sabbatical of 3 to 6 months (after 2 years of service)
  • Free food and beverages at all offices
  • Life Insurance
  • Health Insurance and Employee Assistance Programme
  • Employee Support Networks – help us continue to build on our inclusive culture
  • Flexible and hybrid work


Does this sound like you?

It is time to apply, and we can’t wait to hear from you

Even if you don't meet 100% of the requirements, be confident in yourself and don't hesitate to apply


PLEASE NOTE: We will be longlisting applications as soon as we receive them, so please apply early to register your interest.

We Are Bionical Emas

We are proud of our people and proud of our achievements. We encourage and hire people with diverse backgrounds, voices, beliefs, and perspectives into our growing global workforce. We do not discriminate on the basis of actual or perceived race, color, creed, religion, national origin, ancestry, citizenship status, age, sex or gender (including pregnancy, childbirth, and pregnancy-related conditions), gender identity or expression (including transgender status), sexual orientation, marital status, military service and veteran status, physical or mental disability, genetic information, or any other characteristic protected by applicable federal, state or local laws and ordinances. Bionical Emas’ management team is dedicated to this policy with respect to recruitment, hiring, placement, promotion, transfer, training, compensation, benefits, employee activities, access to facilities and programs, and general treatment during employment.


Bionical Emas offers equal opportunities and is committed to diversity in its workplace and providing accessibility accommodations to applicants with physical and/or mental disabilities. If you are interested in applying for employment with Bionical Emas and need accommodation or special assistance, please let us know by sending an email with your request to the recruitment team at


We Are Bionical Emas, where each person is unique. We celebrate individuality while encouraging our talents to work as a team. Together, we make a difference by powering an inclusive future for all. Be you, with us.


Protecting your privacy and the security of your data is a longstanding top priority for us. Please consult our Privacy Notice to know more about how we collect, use, and transfer the personal data of our candidates. Our Privacy Notice explains what personal information we may process, where we may process your personal information, our purposes for processing your personal information, and the rights you can exercise over Bionical Emas’ use of your personal information. By applying for the above position, you confirm that you have reviewed and agreed to our Data Privacy Notice for Candidates: Privacy Policy - Bionical Emas applicable to your place of residence.