Senior Manager, Regulatory Affairs

3 days ago

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Recruiting.com

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Recruiting. com is a recruitment platform that collects personal and non-personal information from job seekers to be used by recruiters and hiring managers. Users can submit their resumes or fill out a short form to be considered for current and future job opportunities. The site emphasizes user privacy and allows users to manage their personal data, including modifying, changing, and deleting their information. Recruiting. com securely stores user data until they request deletion, providing a comprehensive recruitment solution for both job seekers and employers.

career sites • recruiting software • employment brand • candidate relationship management • talent community

11 - 50 employees

🎯 Recruitment

☁️ SaaS

🤝 B2B

💰 Private Equity Round on 2006-06

📋 Description

• Support change applications (Administrative, Labelling, CMC, Safety) including submission strategy • Dossier compilation including preparation of documents (e.g. local forms, Cover Letters) and Table of Contents • Content review of CMC/Labelling documentation/Justification documents • Alignment with functions on variation procedures, deficiency letter, e.g, CMC, Medical Science, publishing team • Update/local PI (Labelling translation) • Check regulatory compliance of product information/artworks • Marketing Authorization withdrawal • Marketing Authorization Holder transfer • Licence renewal • PSUR contribution • Invoice check (e.g. Authority invoices) • Request Translation/additional M1 documents, e.g. QP declaration, GMP • Databases maintenance: archiving, tracking • Management of local RA requirements (local regulatory intelligence) • NCA electronic systems for submission as locally required • Contact with the local Health Authority on behalf of the client • Cross-functional communication to all relevant departments in relation to regulatory strategy and submission as well as issues related to LCM activities • Support of Country RA Head in issue management (e.g. PQCS Quality, Safety issues like stock out situations management, DHCPL preparation coordination and submission in accordance with local regulations and company SOP, represent RA in internal meetings and committees) • Review of Promotional Materials

🎯 Requirements

• Life Science Degree (Pharmacy degree preferable) • At least 5-10 years of relevant experience in Regulatory Affairs • Experience in the life cycle management of medicinal products and knowledge of the Health Authority requirements for the maintenance of medicinal product licences • Regulatory strategy for successful submission to the Health Authority • Experience in artwork management and supply strategy • Communication with other local functions (Medical Affairs, Pharmacovigilance, Supply)

🏖️ Benefits

• Benefit offerings outside the US may vary by country and will be aligned to local market practice. • The eligibility and effective date may differ for some benefits and for team members covered under collective bargaining agreements.