Overview
Do you want to play a key role in ensuring compliance and smooth market access in pharmaceutical parallel trade? Join our Regulatory Affairs team and help us secure licenses and prepare packaging materials that put patient safety first.
Responsibilities
- Prepare and submit dossiers to acquire and maintain parallel trading licenses.
- Create and maintain packaging materials, artwork files, mock-ups, and item lists.
- Proofread packaging components, application files, and item lists to ensure accuracy.
- Manage and archive regulatory documentation, including packaging materials and authority-approved files.
- You will communicate directly with health authorities and external printing houses, monitor regulatory updates, and implement changes as required.
- Beyond your daily responsibilities, you will contribute to continuous improvement projects, training, and updates of working instructions and guidelines.
- Ad-hoc assignments from your manager may also be part of your role.
About you
We are looking for a detail-oriented and proactive professional who thrives in a structured, regulated environment and enjoys collaborating with multiple stakeholders.
You bring
- A Master’s or Bachelor’s degree in Pharmacy, Regulatory Affairs, Life Sciences, or an equivalent field.
- Minimum 2 years of experience in the pharmaceutical industry.
- Professional proficiency in English (B2 level or higher).
- Experience in at least one of the following areas:
- QA or RA within pharma.
- Interaction with regulatory authorities.
- Handling medicine forms and packaging materials in repackaging processes.
- Experience with repackaging processes and machinery.
- Proficiency in Adobe InDesign, Illustrator, Photoshop; knowledge of EULER (braille) and text comparison software.
- Fluent in English (written and verbal).
- Residence in the country where the role is based and a valid work permit.
Skills and competencies
We expect strong knowledge of regulatory dossiers and parallel distribution procedures and a solid understanding of packaging material design, proofreading, and archiving. You communicate effectively with authorities and external partners, and your work is characterised by accuracy and attention to detail in regulatory submissions. You are able to perform under strict guidelines and deadlines, while also maintaining a continuous improvement mindset, always seeking opportunities to optimise processes and systems.
Are you interested?
We would love to hear from you if you want to be part of an international team ensuring compliance, efficiency, and patient safety. Please submit your CV via our career page.
About us
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Moving Healthcare. Moving You.
In Abacus Medicine Group, you\'ll experience the power of Moving Healthcare. With our change mindset, we\'re moving the industry and improving healthcare as we broaden access to medicine. But it\'s not just about moving healthcare, it\'s about Moving You. You\'ll be part of a caring community of more than 1,500 people across the World. With us, you will be valued, empowered, and have a direct impact on driving change. Let\'s access the future of medicine and make a difference together. Your move.
Department Regulatory Locations Farnborough Employment type Full-time
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