Senior Regulatory Affairs Associate

2 weeks ago


Uxbridge, United Kingdom Park Street People Full time

Our client, a global pharmaceutical company, is currently looking for a Senior Regulatory Affairs Associate - Labelling to join their team in Uxbridge.


Working in a busy global department, there is a focus on working together to achieve results. You would be joining a company with an exciting pipeline who are continually developing their drug portfolio.


As a Senior Regulatory Affairs Associate in Labelling, you will play a crucial role in ensuring regulatory compliance and accuracy in product labelling. You will collaborate closely with cross-functional teams to develop, review, and manage labelling content for our diverse portfolio of pharmaceutical products.


Key Responsibilities

  • Supporting labelling strategies in alignment with regulatory requirements and company objectives
  • Reviewing labelling materials to ensure accuracy and compliance with regulatory standards
  • Provide regulatory guidance and support to internal stakeholders, including product development teams, quality assurance, and manufacturing


Requirements

  • Previous experience in Regulatory Affairs within the pharmaceutical industry, with specific expertise in labelling
  • Strong knowledge of global regulatory requirements and guidelines related to pharmaceutical labelling
  • Excellent communication and interpersonal skills, with the ability to collaborate effectively across multidisciplinary teams
  • Proven ability to manage multiple projects simultaneously and drive initiatives to completion within established timelines
  • Detail-oriented approach with a commitment to accuracy and compliance


Park Street People Ltd is an Equal Opportunities Employer. We do not discriminate on the grounds of age, race, gender, disability, creed or sexual orientation and comply with all relevant UK legislation. We are acting as an Employment Business in relation to this role.



  • Uxbridge, United Kingdom ProClinical Full time

    **Salary**: £240 - £290 per day Job type: ContractDiscipline: Officer /Associate**Location**: United Kingdom- Uxbridge, England - Posting date: 23 Feb 2024 Reference: 59121 Proclinical are recruiting for a Regulatory Affairs Associate to join a pharmaceutical organisation. This role is on a contract basis and is either located in Uxbridge or...


  • Uxbridge, United Kingdom Park Street People Full time

    **Our client, a global pharmaceutical company, is currently looking for a CMC Regulatory Affairs Associate to join their team in Uxbridge.** Working in a busy global department, there is a focus on working together to achieve results. You would be joining a company with an exciting pipeline who are continually developing their drug portfolio. This is a...


  • Uxbridge, United Kingdom Amgen Full time

    Career Category Regulatory **Job Description**: - Job Description: - Amgen is a leading human therapeutics company in the biotechnology industry. For more than 40 years, the company has tapped the power of scientific discovery and innovation to advance the practice of medicine. As a Fortune 500 company serving millions of patients. Amgen continues to be...


  • Uxbridge, United Kingdom CK Group- Science, Clinical and Technical Full time

    CK Group are recruiting for a Regulatory Affairs Manager to join a biopharmaceutical company who are based in Uxbridge on a contract basis for 12 months. Company: Our client is committed to unlocking the potential of biology for patients suffering from serious illnesses by discovering, developing, manufacturing and delivering innovative human...


  • Uxbridge, United Kingdom Park Street People Full time

    An innovative global pharmaceutical company is currently looking for a Regulatory Affairs Manager with CTA, EU and early stage development experience to join their team on a 12 month temporary contract. Working with the regulatory team (and core stakeholders across multiple areas), your role will be to provide regulatory strategy and guidance across the...


  • Uxbridge, United Kingdom CK Group- Science, Clinical and Technical Full time

    CK Group are recruiting for a Regulatory Affairs Manager to join a biopharmaceutical company who are based in Uxbridge on a contract basis for 12 months.Company:Our client is committed to unlocking the potential of biology for patients suffering from serious illnesses by discovering, developing, manufacturing and delivering innovative human therapeutics....


  • Uxbridge, United Kingdom Park Street People Full time

    An innovative global pharmaceutical company is currently looking for a Regulatory Affairs Manager with CTA, EU and early stage development experience to join their team on a 12 month temporary contract. Working with the regulatory team (and core stakeholders across multiple areas), your role will be to provide regulatory strategy and guidance across the...


  • Uxbridge, United Kingdom CK Group Full time

    CK Group are recruiting for a Regulatory Affairs Manager to join a biopharmaceutical company who are based in Uxbridge on a contract basis for 12 months. Company: Our client is committed to unlocking the potential of biology for patients suffering from serious illnesses by discovering, developing, manufacturing and delivering innovative human therapeutics....


  • Uxbridge, United Kingdom Park Street People Full time

    An innovative global pharmaceutical company is currently looking for a Regulatory Affairs Manager with CTA, EU and early stage development experience to join their team on a 12 month temporary contract. Working with the regulatory team (and core stakeholders across multiple areas), your role will be to provide regulatory strategy and guidance across the...


  • Uxbridge, United Kingdom Park Street People Full time

    An innovative global pharmaceutical company is currently looking for a Regulatory Affairs Manager with CTA, EU and early stage development experience to join their team on a 12 month temporary contract. Working with the regulatory team (and core stakeholders across multiple areas), your role will be to provide regulatory strategy and guidance across the...


  • Uxbridge, United Kingdom Park Street People Full time

    An innovative global pharmaceutical company is currently looking for a Regulatory Affairs Manager with CTA, EU and early stage development experience to join their team on a 12 month temporary contract. Working with the regulatory team (and core stakeholders across multiple areas), your role will be to provide regulatory strategy and guidance across the...


  • Uxbridge, United Kingdom Park Street People Full time

    An innovative global pharmaceutical company is currently looking for a Regulatory Affairs Manager with CTA, EU and early stage development experience to join their team on a 12 month temporary contract. Working with the regulatory team (and core stakeholders across multiple areas), your role will be to provide regulatory strategy and guidance across the...


  • Uxbridge, United Kingdom Park Street People Full time

    Job DescriptionAn innovative global pharmaceutical company is currently looking for a Regulatory Affairs Manager with CTA, EU and early stage development experience to join their team on a 12 month temporary contract. Working with the regulatory team (and core stakeholders across multiple areas), your role will be to provide regulatory strategy and guidance...


  • Uxbridge, Greater London, United Kingdom CK Group- Science, Clinical and Technical Full time

    CK Group are recruiting for a Regulatory Affairs Manager to join a biopharmaceutical company who are based in Uxbridge on a contract basis for 12 months. Our client is committed to unlocking the potential of biology for patients suffering from serious illnesses by discovering, developing, manufacturing and delivering innovative human therapeutics. This...


  • Uxbridge, United Kingdom PE Global Full time

    PE Global is recruiting a Regulatory Affairs Manager (CTA) for our multinational pharmaceutical client based in Uxbridge. The role is hybrid and an initial 12-month contract.In order to make an application, simply read through the following job description and make sure to attach relevant documents.Responsibilities of the role: Advising the GRT on regional...


  • Uxbridge, United Kingdom Park Street People Full time

    Our client, a global pharmaceutical company, is currently looking for a CMC Regulatory Affairs Manager to join their team in Uxbridge on a temporary contract. This is a great opportunity to work for a pharmaceutical company who have created a centre of excellence and constantly focus on driving innovation and using cutting edge techniques in their...


  • Uxbridge, Greater London, United Kingdom CK Group- Science, Clinical and Technical Full time

    CK Group are recruiting for a Regulatory Affairs Manager to join a biopharmaceutical company who are based in Uxbridge on a contract basis for 12 months. Company: Our client is committed to unlocking the potential of biology for patients suffering from serious illnesses by discovering, developing, manufacturing and delivering innovative human...


  • Uxbridge, Greater London, United Kingdom Park Street People Full time

    An innovative global pharmaceutical company is currently looking for a Regulatory Affairs Manager with CTA, EU and early stage development experience to join their team on a 12 month temporary contract. Working with the regulatory team (and core stakeholders across multiple areas), your role will be to provide regulatory strategy and guidance across the...


  • Uxbridge, United Kingdom Park Street People Full time

    Our client, a global pharmaceutical company, is currently looking for a CMC Regulatory Affairs Manager to join their team in Uxbridge on a temporary contract.This is a great opportunity to work for a pharmaceutical company who have created a centre of excellence and constantly focus on driving innovation and using cutting edge techniques in their science.Key...


  • Uxbridge, United Kingdom Parexel Full time

    When our values align, there's no limit to what we can achieve.   We are looking for a Senior Consultant Regulatory Affairs for Labelling . This is a client dedicated role. The role can be based in multiple locations in UK and EU (home or office based). In this role you will partner with Label Strategist to: Conduct international labeling...