CMC Regulatory Affairs Manager

We want to change this state of affairs because every person is important to us.

Fondazione Telethon ETS is currently searching for a CMC Regulatory Affairs Manager.

The candidate will work in the Research and Development Department on specific Telethon’s projects in late development/marketing phase (Strimvelis, Telethon003) as well as Telethon’s Institutes’ (TIGET and TIGEM) projects in early/mid development phase.

The candidate will have the following responsibilities:

• Support the CMC Regulatory Team: Help the team implement and manage CMC regulatory strategies for gene therapy projects, ensuring everything aligns with regulatory requirements. Contribute to the regulatory strategy for clinical trials and commercial products by preparing CMC sections of regulatory dossiers, performing gap analyses, and helping address any missing information.
• Assist with Regulatory Authorities Inspections: Provide support during Regulatory Authorities inspections by ensuring that all necessary CMC regulatory information for investigational and commercial products is organized and compliant.
• Support in the preparation and documentation of regulatory submissions:Assist in preparing and managing CMC aspects of regulatory documents for assigned projects, including managing CMC-related requests for Orphan Drug Designation (ODD), Scientific Advice, and Pediatric Investigation Plans (PIP). Contribute to initial regulatory submissions for clinical trials and commercial products, and support the regulatory process throughout the product lifecycle, including submissions for changes to marketing authorizations (MAA/BLA) and investigational product dossiers (IMPD/IND).
• Monitor Regulatory framework: Stay on top of regulatory updates and contribute to the team’s strategy to ensure we always meet the latest standards, especially for orphan drugs, advanced therapies (ATMP), GMP, and compliance.
• Collaborate with CMC and Quality Assurance Teams: Ensure compliance of GMP documents to regulatory commitments and provides support for batch release process (review/approval deviations, status of approval of change etc.). Work in collaboration with the Quality Assurance and CMC teams to evaluate any events affecting product quality, such as deviations or out-of-specification results, and help managing change controls performing the regulatory impact assessment.
• Bachelor’s or Master’s degree in Pharmacy, Biotechnology, Chemistry, Biology, Pharmaceutical Sciences, or a related life sciences field.
• Previous experience (ideally, 5-7 years of experience) in Regulatory Affairs, GMP, or CMC in the pharmaceutical or biotech industry;
• Previous experience with Cell&Gene Therapies;
• Excellent English oral and written communication skills;
• Ability to work autonomously and prioritize workflow;
• Demonstrated analytical, problem resolution and communication skills.
• Strong communication and organizational skills to manage regulatory documents and collaborate with global regulatory bodies.
• Attention to detail, with the ability to manage multiple tasks in a regulated environment.

Salary

RAL and type of contract will be commensurate with seniority.

Workplace

Milan, hybrid.

We will only consider candidates who will attach their Resume when applying.

We thank you in advance for expressing your interest in the Organization. We inform you that, due to the huge amount of applications received, we will be able to provide a feedback only to those who will be contacted from Fondazione Telethon.