Regulatory Affairs Executive

Job title:

Regulatory Affairs Executive

Company

Takeda

Job description

By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda’s and . I further attest that all information I submit in my employment application is true to the best of my knowledge.Job DescriptionTakeda is committed to fostering a diverse and inclusive workplace, valuing the unique backgrounds and perspectives of our employees. We proudly support our Takeda Resource Groups (TRG), employee-led networks promoting dialogue and professional growth. We encourage all candidates, regardless of background, to apply and explore opportunities to contribute to and benefit from our TRGs and inclusive initiatives. We are dedicated to providing accommodations and support during the recruitment process.For Takeda UK and Ireland, we are looking for a Regulatory Affairs Executive who will be responsible for providing technical and administrative regulatory support for the company’s product portfolio in the UK and Ireland.Key duties include maintaining and obtaining marketing authorizations, ensuring compliance with national and EU drug laws, collaborating with local and global teams, and keeping up to date with regulatory legislation and guidelines.KEY RESPONSIBILITIESFollowing direction from manager, to provide support across the RA team with the following activities:Regulatory Applications: Prepare, compile, and submit regulatory applications for UK/IE, including managing fee requests, preparing submission documentation, and liaising with publishing.Post-Submission Actions: Update electronic systems, notify commercial teams, and respond to regulatory commitments or requests.Regulatory Approvals Management: Implement product information changes, manage approved mock-ups, and notify relevant parties of approvals.Regulatory Contact Point: Interact with local and global teams, manage direct interactions with regulatory authorities, and provide regulatory advice.Other Duties: Support tender requests, HTA submissions, shortage notifications, unlicensed medicines requests, and review and update SOPs.EDUCATION, EXPERIENCE AND SKILLSRequiredBSc in a scientific discipline.Minimum of 3 years in the pharmaceutical industry, experience with UK or Ireland Regulatory Authorities, preparing and submitting regulatory applications, and writing clear product information documents.Ability to handle multiple tasks, excellent organizational and time management skills, computer literacy, effective communication, problem-solving, and attention to detail.DesiredAbility to assess risks, desire to develop within the role, and interest in networking to raise the profile of the regulatory function/Takeda.Enthusiastic, confident and proactive. Shows initiative and a sense of urgency.Can do attitudeEmpowering our people to shineAt Takeda, we earn the trust of society and our customers through our values of Takeda-ism: Integrity, Fairness, Honesty, Perseverance. We incorporate these values in everything we do. They represent who we are and how we act. They help us make decisions that we can be proud of today and in the future. We enable our employees to develop their full potential. As a global top employer, we offer exciting career paths, promote innovation, and strive for top performance in everything we do. Takeda fosters an inclusive, collaborative, and international work environment where our teams are united by their relentless commitment to our goal of improving people’s health and creating a better future for the world.Diversity, Equality, and InclusionTakeda is committed to foster diversity, equality, and inclusion. Hiring decisions are based entirely on qualifications and are made regardless of gender, ethnic origin, religion, sexual orientation, age, or disability.If you are interested in this opportunity, we look forward to receiving your application via our online tool!Learn more atLocations GBR – PaddingtonWorker Type EmployeeWorker Sub-Type RegularTime Type Full time

Expected salary

Location

Paddington, West London

Job date

Fri, 29 Nov 2024 02:45:39 GMT

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