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About the role
Key responsibilities & impact- Support Cross-Functional European Projects to drive innovation and efficacy
- Manage diverse maintenance activities of Medicinal Product Licenses (e.g., UK, IE) and export market, like:
- Preparation and submission of variations
- Creation and revision of packaging & promotional materials
- Update of internal and official databases
- Support audits & inspections
- Support the Pharmacovigilance system
- Monitor regulatory/pharmaceutical regulations for the relevant therapeutic areas and share information internally
- Assist other functions, like customer service and tender business with regulatory expertise
Requirements
What you’ll need- Bachelor’s degree or equivalent, preferably in life sciences (pharmacy, biology, or similar)
- Experience (minimum 2 years) of being in a similar position in the pharmaceutical industry or at health authorities
- Good knowledge of applicable pharmaceutical regulations – preferably with UK & EU registration procedures
- Basic knowledge of related ethical code of practice required for GXP compliance
- Strong written and verbal communication and organizational skills
- Ability to work independently and collaborate effectively with cross-functional colleagues at all levels of the organization
- Ability to multi-task and prioritize work
- Fluency in English (speaking, reading, and writing)
- Proficiency in Microsoft applications (Excel, Word, PowerPoint)
Benefits
Comp & perks- Hybrid working model optional
ATS Keywords
✓ Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills & Tools
regulatory compliancepharmaceutical regulationsGXP compliancePharmacovigilancepreparation and submission of variationspackaging and promotional materials creationdatabase management
Soft Skills
strong written communicationstrong verbal communicationorganizational skillsindependent workcollaborationmulti-taskingprioritization