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- Tasks: Review labels and artwork, ensuring accuracy and compliance with regulations.
- Company: Join a leading biopharmaceutical company dedicated to innovative treatments for rare diseases.
- Benefits: Enjoy flexible remote work, career growth opportunities, and diverse benefits.
- Why this job: Make a meaningful impact in the rare disease community while collaborating with experts.
- Qualifications: Graduate or undergraduate level with 4-6 years in Pharma or Medical Devices.
- Other info: Work from anywhere in Europe and access training for personal and professional development.
The predicted salary is between 28800 - 48000 £ per year.
The Regulatory Labelling and Artwork Specialist role is part of a project with a leading biopharmaceutical company focused on developing innovative treatments for rare and ultra-rare genetic diseases. If you are passionate about working with a renowned organization committed to advancing research and supporting patients and families affected by these conditions, we encourage you to apply. This position offers the opportunity to collaborate with healthcare professionals, researchers, and advocacy groups, making a meaningful impact in the rare disease community. The role is fully remote and can be performed from anywhere in Europe. Join us and be part of our inspiring journey of growth!
Responsibilities:
- Conduct thorough reviews of labels and artwork, ensuring accuracy in translation, quality control, and proofreading.
- Oversee Structured Product Labeling (SPL) processes, manage life cycles, and handle key documents such as USPI and MSPC.
- Provide broad-level support for labelling operations across multiple countries, ensuring compliance with global and regional regulations.
Requirements:
- Educational background of Graduate or Undergraduate level.
- 4-6 years of experience in the Pharma or Medical Devices industry.
- Proficiency in global and regional labelling and artwork regulations.
- Experience in handling artwork and label quality control (QC) and proofreading.
- Familiarity with Structured Product Labeling (SPL) and labelling life cycle management.
- English language proficiency at B2/C1 level.
- Prior experience with biologicals is a plus but not mandatory.
Benefits:
- Opportunity to work in a fast-growing company and in a multinational environment for some of the biggest brands in the world.
- Potential for career growth within the organization and the opportunity to build a successful career path.
- Flexible and fully remote work environment, allowing you to work from the comfort of your home in any city in Europe.
- Access to a diverse range of benefits.
- Personal and professional development through a variety of training programs covering both hard and soft skills.
- Comprehensive salary package with various components.
- Complex reward and recognition schemes (both non-monetary and monetary options).
- Referral schemes.
Regulatory Labelling and Artwork Specialist employer: Wipro Digital Operations and Platforms
Contact Detail:
Wipro Digital Operations and Platforms Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Regulatory Labelling and Artwork Specialist
✨Tip Number 1
Familiarise yourself with the latest global and regional labelling regulations. This knowledge will not only help you in interviews but also demonstrate your commitment to compliance, which is crucial for this role.
✨Tip Number 2
Network with professionals in the biopharmaceutical industry, especially those involved in regulatory affairs. Engaging with them can provide insights into the role and may even lead to referrals.
✨Tip Number 3
Showcase your experience with Structured Product Labeling (SPL) during discussions. Be prepared to discuss specific projects where you've managed labelling life cycles or quality control processes.
✨Tip Number 4
Prepare thoughtful questions about the company's approach to rare diseases and their labelling processes. This shows your genuine interest in the role and the impact it has on patients and families.
We think you need these skills to ace Regulatory Labelling and Artwork Specialist
Some tips for your application 🫡
Understand the Role: Before applying, make sure you fully understand the responsibilities and requirements of the Regulatory Labelling and Artwork Specialist position. Tailor your application to highlight relevant experience in labelling and artwork regulations.
Highlight Relevant Experience: In your CV and cover letter, emphasise your 4-6 years of experience in the Pharma or Medical Devices industry. Be specific about your familiarity with Structured Product Labeling (SPL) and any quality control processes you've managed.
Showcase Language Proficiency: Since English proficiency at B2/C1 level is required, ensure that your application reflects your language skills. Use clear and professional language throughout your CV and cover letter.
Personalise Your Cover Letter: Craft a compelling cover letter that expresses your passion for working in the biopharmaceutical sector and your commitment to supporting patients with rare diseases. Mention how your skills align with the company's mission and values.
How to prepare for a job interview at Wipro Digital Operations and Platforms
✨Know Your Regulations
Familiarise yourself with global and regional labelling and artwork regulations. Being able to discuss these in detail will show your expertise and understanding of the role's requirements.
✨Showcase Your Experience
Prepare specific examples from your 4-6 years in the Pharma or Medical Devices industry. Highlight your experience with quality control, proofreading, and managing labelling life cycles to demonstrate your capability.
✨Emphasise Collaboration Skills
Since the role involves working with healthcare professionals and advocacy groups, be ready to discuss how you’ve successfully collaborated in past projects. This will illustrate your ability to work effectively in a team.
✨Ask Insightful Questions
Prepare thoughtful questions about the company’s projects and their impact on the rare disease community. This shows your genuine interest in the role and the organisation's mission.
