proven experience in a pharmaceutical regulatory affairs environment including compilation and submission experience of working in several groups in regulatory affairs or experience at a health authority. Implement business priorities. License maintenance: Ensure all post-approval product maintenance activities including technical changes to the label or the packs, PBRERs, and post approval commitments are submitted and approved
proven experience in a pharmaceutical regulatory affairs environment including compilation and submission experience of working in several groups in regulatory affairs or experience at a health authority. Implement business priorities. License maintenance: Ensure all post-approval product maintenance activities including technical changes to the label or the packs, PBRERs, and post approval commitments are submitted and approved
development, commercialization and regulatory affairs, including conceptualization, design, and execution product development commercialization and regulatory affairs, including conceptualization, design, and execution development and commercialization and regulatory affairs Ability to collaborate remotely with team members
development, commercialization and regulatory affairs, including conceptualization, design, and execution product development commercialization and regulatory affairs, including conceptualization, design, and execution development and commercialization and regulatory affairs Ability to collaborate remotely with team members