Related skills
regulatory affairs gxp pharmaceuticals regulatory submissions documentation management📋 Description
- Support new applications for marketing authorization, renewal, or variation of products.
- Publish and submit product registration applications.
- Coordinate activities to keep registration information accurate and current.
- Support compilation, tracking, indexing and archival of regulatory documents.
- Specify storage, labeling and packaging requirements for regulated products.
- Create, update, review and quality-check product labels.
🎯 Requirements
- Bachelor’s degree in Life Science (Chemistry/Biology/Biomedical Eng)
- Experience in regulatory affairs is a plus
- Fluency in English
- Ability to meet deadlines under pressure
- Strong teamwork and problem-solving skills
🎁 Benefits
- Flexible working hours
- Performance development with year-end reviews
- Team events and year-end party
- Employee feedback survey for continuous improvement
- Health insurance
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