Regulatory Affairs Specialist – French-Speaking (Part-Time)

mpharma in Birmingham is seeking a part-time Regulatory Affairs professional to handle conformable regional regulatory tasks. The role involves understanding sterile and radio-pharmaceutical products, and managing MA filings and compliance across Europe and ROW.

The candidate will file dossiers, respond to health authority questions, and oversee post-MA maintenance, packaging text validation, SOPs, and audits. This position offers a contract starting part-time with potential permanency.

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