Global Labelling Lead

Global Labelling Lead

Full-Time 70000 - 90000 £ / year (est.) Home office (partial)
Doist

At a Glance

  • Tasks: Lead global product labeling strategy and ensure compliance across markets.
  • Company: Dynamic biopharmaceutical company focused on patient-centric solutions.
  • Benefits: Flexible working options, competitive salary, and opportunities for professional growth.
  • Other info: Join a diverse team and contribute to impactful global projects.
  • Why this job: Make a real difference in patient care through innovative labeling strategies.
  • Qualifications: Experience in regulatory affairs and strong collaboration skills required.

The predicted salary is between 70000 - 90000 £ per year.

The Global Labeling Lead (GLL) serves as a labeling strategy expert for Sobi products within Global Regulatory Affairs (GRA).

This role can be located in several countries in Europe and Switzerland, depending on where the chosen candidate will be located.

The GLL provides both strategic and operational leadership for product labeling, working closely with Regulatory Strategy Leads and other cross‑functional stakeholders.

As a core member of the Global Regulatory Team(s) (GRT) for assigned product(s), the GLL ensures that product labeling reflects scientific integrity, regulatory compliance, and patient focus across global markets.

Lead the content development, approval, and maintenance of the Company Core Data Sheet (CCDS) and US/EU Product Information (PI).

Manage the review and approval of country labeling for new filings in international markets.

Ensure compliance with relevant Health Authority (HA) regulations, internal procedures, and business objectives.

Support continuous improvement of labeling processes and systems.

Key Responsibilities

  • Lead the development, implementation, and maintenance of the CCDS, USPI and EU PI for assigned Sobi products throughout the product lifecycle via cross‑functional Labeling Working Groups (LWG).
  • Guide LWGs in labeling discussions with HAs, while ensuring management alignment and adherence to labeling governance.
  • Collaborate closely with internal stakeholders and partner companies, as applicable, and document and archive LWG decisions and outcomes.
  • Present new labeling content and major updates to the Executive Labeling Committee for approval.
  • Partner with international Regulatory Affairs (RA) to guide the review and approval process of labels for submission outside of EU and US.
  • Maintain oversight of labeling compliance, including documentation of labeling content deviations and end‑to‑end tracking of safety variations.
  • Contribute to the development and improvement of labeling processes, including creation and review of process documents.
  • Support inspections and audits related to labeling activities.
  • Participate in cross‑functional and cross‑regional initiatives to strengthen collaboration and increase operational efficiencies.
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Global Labelling Lead employer: Doist

Brink's is an exceptional employer that fosters a collaborative and innovative work culture, empowering employees to drive global commercial strategies in the ATM lifecycle solutions sector. With a strong focus on professional development and growth opportunities, employees are encouraged to expand their skills while contributing to sustainable growth and operational excellence. Located in a dynamic environment, Brink's offers unique advantages such as a diverse team and the chance to build long-term partnerships with global customers, making it a rewarding place to advance your career.

Doist

Contact Details:

Doist Recruitment Team

StudySmarter Expert Advice🤫

We think this is how you could land Global Labelling Lead

Unlock Networking Opportunities

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Tailor Your Approach

When you're applying for roles, don't rush it! Take the time to customise your applications for specific positions, showcasing relevant skills and experiences that align with what Doist is looking for. A tailored application can really make you stand out!

We think you need these skills to ace Global Labelling Lead

Labeling Strategy Expertise
Regulatory Compliance
Cross-Functional Collaboration
Content Development
Approval Processes
Health Authority Regulations
Continuous Improvement

Some tips for your application 🫡

Showcase Your Relevant Experience:When applying for a role in the pharmaceutical industry, it's crucial to highlight any relevant experience you have. Whether that's internships, lab work, or even related coursework, make sure to weave this into your CV and cover letter. We want to see how your background aligns with the role you're applying for at Doist!

Emphasise Your Understanding of Regulations:The pharmaceutical industry is heavily regulated, so it's important to indicate your familiarity with industry standards and regulations. In your cover letter, mention any training or certifications you've received that are relevant, or discuss projects where you’ve navigated compliance. This will show Doist that you're not just a fit for the job but also a safety-conscious candidate!

Tailor Your CV to Be Result-Driven:Craft your CV to highlight quantifiable achievements, especially if you have previous roles in pharmaceuticals or related fields. Use metrics to demonstrate your impact, such as improved processing times or successful project completions while working on trials. This analytical approach will resonate well with hiring managers at Doist!

Convey Your Passion for the Industry:In your cover letter, express why you are passionate about working in the pharmaceutical sector. Whether it’s your desire to contribute to groundbreaking drug research or improve patient outcomes, let it shine through! At Doist, we value candidates who are truly enthusiastic about their work—you might just stand out from the crowd.

How to prepare for a job interview at Doist

Understand the Science

Make sure you brush up on key pharmaceutical concepts and recent developments in the industry. You might get asked some technical questions during the interview at Doist that show your grasp of drug development processes or regulatory requirements, so be ready to discuss them clearly.

Showcase Relevant Experience

If you have any hands-on experience or internships in a laboratory setting, be sure to highlight these in your responses. Think about the projects you worked on, the methodologies you used, and the impact you made. It's all about telling a story that connects your background to the role you're applying for.

Know Their Products

Take some time to familiarise yourself with Doist’s product range and recent breakthroughs. Understanding their portfolio not only shows your enthusiasm for the role but also allows you to ask insightful questions that demonstrate your interest in actively contributing to their projects.

Be Ready for Regulatory Scenarios

In a full-time pharmaceutical role, understanding the regulatory landscape is crucial. Prepare for situational questions that may test your problem-solving skills concerning compliance and safety standards. You could be asked how you'd handle a hypothetical issue regarding a drug’s market release, so think through your approach.