At a Glance
- Tasks: Lead global labelling operations and collaborate with teams to ensure compliance and efficiency.
- Company: Join a leading biotech company dedicated to improving global health.
- Benefits: Competitive salary, inclusive culture, and opportunities for professional growth.
- Other info: Dynamic work environment with a focus on teamwork and global collaboration.
- Why this job: Make a real impact in the pharmaceutical industry while working on innovative projects.
- Qualifications: Degree in Life Sciences and experience in regulatory or labelling roles.
The predicted salary is between 60000 - 80000 £ per year.
Manager, Global Labelling Operations (GLO) is part of a team of labelling professionals responsible for managing and executing the technical and operational elements that support the development, review and approval of product packaging components globally, to meet business objectives.
This position is a key partner to Global Regulatory Affairs Regions and Supply Chain and plays a pivotal role in ensuring efficient labelling operations support for regulatory submissions and product supply, including time‑critical annual strain updates for Seqirus’ seasonal influenza vaccines portfolio.
- Main Responsibilities & Accountabilities
- Regulatory lead for the development, approval and maintenance of printed artwork for Seqirus’ marketed products globally.
- Collaborates with key stakeholders within regulatory affairs and other parts of the business (e. g.
Commercial, Supply Chain, Quality Assurance, Project Management) to ensure timely development of artworks for regulatory submissions, in compliance with GMP.
- Provides tactical and strategic guidance to regional product labelling teams regarding placement and regulatory requirements for regional packaging component labelling content and design.
- Manages/inputs into process development, the establishment and maintenance of labelling systems, and compilation of performance and compliance metrics associated with labelling operations.
- Identifies and manages the implementation of operational improvements to ensure business excellence for Seqirus in all aspects of labelling operations.
- Provides operational training within Regulatory.
- Remains up to date with the global labeling requirements and expectations.
Qualifications & Experience
- University degree in Life Sciences or related pharmaceutical field.
- Ability to work in a rapid‑paced environment.
- Biotech/pharmaceutical industry experience, including labelling/regulatory combined with other global responsibility.
- Knowledge and understanding of principles of regulatory requirements relevant to drug development, global labeling and post‑marketing requirements.
- Demonstrated problem‑solving ability, ability to analyze risk and make appropriate recommendations/decisions.
- Must work well with others and within global teams, particularly cross‑cultural exposure. Experience working in a complex and matrix environment is required.
- Excellent customer focus with demonstrated management of customer expectations and anticipating customer needs.
- Organizational skills to interact seamlessly with stakeholders on regulatory compliance matters.
- Effective verbal and written communication skills in a cross‑functional environment.
- Attention to detail, coupled with the ability to think strategically.
- Fluency in English (verbal and written).
- Equal Opportunity Employer
CSL is an Equal Opportunity Employer. If you are an individual with a disability and need a reasonable accommodation for any part of the application process, please visit
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Manager, Labeling Operations in Maidenhead employer: CSL
As an Associate Director in Procurement Enablement at CSL, you will be part of a forward-thinking organisation that prioritises sustainability and governance while fostering a culture of continuous improvement and talent development. With a commitment to employee growth through the Global Procurement Academy and a collaborative work environment, CSL offers a unique opportunity to influence procurement practices on a global scale, making it an excellent employer for those seeking meaningful and impactful careers.
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We think this is how you could land Manager, Labeling Operations in Maidenhead
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We think you need these skills to ace Manager, Labeling Operations in Maidenhead
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 CSL!
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 CSL 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 CSL!
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 CSL, 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 CSL
✨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 CSL 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 CSL’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.
