Regulatory Affairs

Regulatory Affairs

Buckingham Full-Time 36000 - 60000 £ / year (est.) No home office possible
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At a Glance

  • Tasks: Join our team as a Regulatory Affairs Contractor, focusing on OTC medicines and more.
  • Company: Be part of a century-old company dedicated to health and well-being with renowned brands.
  • Benefits: Enjoy a hybrid work model and flexible hours, plus great corporate perks.
  • Why this job: Make an impact in regulatory affairs while working in a supportive and innovative environment.
  • Qualifications: Must be a life sciences or chemistry graduate with project management experience.
  • Other info: Opportunity to mentor others and enhance your professional skills.

The predicted salary is between 36000 - 60000 £ per year.

Regulatory Affairs Contractor – Pharmaceuticals – 6-Month Contract

Our client have an exciting new opportunity for a regulatory affairs contractor to join the team. Our client has specialised in pharmaceutical products and people\’s well-being for over a century and work with some well-known household brands.

Responsibilities:

  • Principle responsibilities will be within Consumer Health OTC medicines but may also include assisting in regulatory support for other product types such as Cosmetics, Medical Devices and Food Supplements.
  • Development of regulatory strategies, preparation of regulatory applications and support maintenance activities within relevant therapy area
  • Supports the team with regulatory activities for National and/or European procedures (Decentralised, Mutual Recognition) as appropriate.
  • Maintain awareness/knowledge of current regulatory legislation.
  • May act as an ambassador for the Regulatory Affairs department to raise profile of team both internally and externally.
  • Requirements:

  • Life sciences or chemistry graduate to honours level or equivalent.
  • Works with minimal supervision to plan, conduct, and manage regulatory submissions and multiple projects to meet department and company objectives.
  • Work with minimal supervision to determine and develop approaches to solutions with technical guidance on a variety of problems of moderate scope and complexity.
  • May mentor Graduate and Regulatory Executive and provide day to day support (as appropriate).
  • Project management, understanding of regulatory environment, interaction with the Regulatory Authorities (as appropriate), commercial / strategic awareness, implement regulatory strategy, managing and maintaining Marketing Authorisations etc
  • Hybrid. 1 – 2 days in the office per week
  • If this role is of interest to you, please apply now!

    #LI-KT1

    Regulatory Affairs employer: Quanta part of QCS Staffing

    Join a leading pharmaceutical company that has been dedicated to enhancing people's well-being for over a century. With a strong focus on employee growth and a collaborative work culture, this role offers the unique opportunity to contribute to impactful regulatory strategies while enjoying a hybrid work model that promotes work-life balance. As part of a dynamic team, you'll have access to mentorship opportunities and the chance to work with renowned household brands in a supportive environment.
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    Contact Detail:

    Quanta part of QCS Staffing Recruiting Team

    StudySmarter Expert Advice 🤫

    We think this is how you could land Regulatory Affairs

    ✨Tip Number 1

    Familiarise yourself with the latest regulatory guidelines and legislation in the pharmaceutical industry. This knowledge will not only help you during interviews but also demonstrate your commitment to staying updated in a rapidly changing field.

    ✨Tip Number 2

    Network with professionals in the regulatory affairs sector, especially those who have experience in Consumer Health OTC medicines. Attend industry events or join relevant online forums to make connections that could lead to valuable insights and potential referrals.

    ✨Tip Number 3

    Prepare to discuss specific examples of your project management experience and how you've successfully navigated regulatory submissions in the past. Being able to articulate your hands-on experience will set you apart from other candidates.

    ✨Tip Number 4

    Showcase your ability to work independently and manage multiple projects effectively. Be ready to provide examples of how you've balanced competing priorities and met deadlines, as this is crucial for the role.

    We think you need these skills to ace Regulatory Affairs

    Regulatory Knowledge
    Project Management
    Technical Writing
    Attention to Detail
    Communication Skills
    Analytical Skills
    Problem-Solving Skills
    Knowledge of Pharmaceutical Regulations
    Experience with Regulatory Submissions
    Understanding of Consumer Health Products
    Ability to Work Independently
    Mentoring Skills
    Commercial Awareness
    Strategic Thinking

    Some tips for your application 🫡

    Understand the Role: Read the job description thoroughly to understand the responsibilities and requirements. Tailor your application to highlight your relevant experience in regulatory affairs, especially in pharmaceuticals.

    Highlight Relevant Experience: In your CV and cover letter, emphasise any previous roles or projects that relate to regulatory submissions, project management, or working with regulatory authorities. Use specific examples to demonstrate your expertise.

    Showcase Your Education: Mention your qualifications clearly, especially if you have a degree in life sciences or chemistry. If you have any additional certifications related to regulatory affairs, include those as well.

    Craft a Compelling Cover Letter: Write a cover letter that not only outlines your skills but also expresses your enthusiasm for the role. Explain why you want to work in regulatory affairs and how you can contribute to the company's goals.

    How to prepare for a job interview at Quanta part of QCS Staffing

    ✨Know Your Regulatory Landscape

    Familiarise yourself with the current regulatory legislation relevant to pharmaceuticals, especially in Consumer Health OTC medicines. Being able to discuss recent changes or trends will show your commitment and knowledge in the field.

    ✨Demonstrate Project Management Skills

    Prepare examples of how you've successfully managed multiple projects in the past. Highlight your ability to work independently and meet deadlines, as this is crucial for the role.

    ✨Showcase Your Technical Knowledge

    Be ready to discuss your understanding of regulatory submissions and the processes involved. This could include your experience with National and European procedures, which will be key in your role.

    ✨Emphasise Team Collaboration

    Since the role may involve mentoring others, be prepared to talk about your experience in team settings. Discuss how you’ve supported colleagues or led initiatives that raised the profile of your previous teams.

    Regulatory Affairs
    Quanta part of QCS Staffing
    Location: Buckingham
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