Job Description Summary: PTC is an established global biopharmaceutical company that strives to deliver transformative therapies for people living with rare diseases. For 25 years, we have been harnessing our scientific platforms to create innovative therapies that address the underlying cause of the disease to deliver on our promise to create more moments for those who count on us.The Associate Manager, Regulatory Affairs – Europe (including UK & Switzerland) is responsible for providing operational support for the planning, management, support and execution of regulatory activities for PTC drug products (clinical and commercial) within Europe. This role includes responsibility for support of regional registration and life cycle management regulatory activities. This individual, collaborates with the Head Regulatory Affairs Europe, the EU Regulatory Team, and works closely with the Vice President, International Regulatory Affairs Management. The role is responsible for ensuring that regional regulatory strategies are executed in compliance withcurrent, applicable regulations and standards.This position works cross-functionally and serves as a liaison between Global Regulatory Affairs team members, other PTC departments, external service providers and contract manufacturers.The Associate Manager, Regulatory Affairs – Europe ensures for adherence to relevant regulatory requirements and company Standard Operating Procedures (SOPs) as appropriate.Job Description:Responsibilities of the role include: In alignment with PTC’s global regulatory strategies, assists in the implementation of regional regulatory strategies for PTC compounds in all stages of clinical and commercial development.Serves as a liaison to regional regulatory Health Authorities and other national authorities and provides guidance and advice on regulatory and policy developments within the region to PTC’s global regulatory team and other key stakeholders. Actively maintains knowledge of regional regulatory requirements (e.g. new regulations, laws, etc.).Supports strategies for, coordinates the execution of, and ensures the proper archival of regulatory submissions including, but not limited to: Clinical Trial Applications (CTAs); Marketing Authorization Approvals (MAAs) including those required to maintain approvals (i.e. variations, renewals) and customized dossiers for the registration of drug products in countries within the region.Provides regulatory support for country specific Early Access Programs (EAPs). This may also include the preparation of supportive regulatory documents for these programs.Collaborates with project teams and other internal and external key stakeholders as appropriate to ensure effective local product registrations. Ensures that drug products distributed with the region meet local regulatory requirements while also supporting PTC’s commercial/business objectives. Provides regulatory support to the Global Pharmacovigilance (PV) organization and regional/country representatives as necessary to ensure that PTC’s PV obligations within the region are met. Supports the co-ordination of contracted activities for translation, submission of regulatory documentation and contact with local Health Authorities. Performs other tasks and assignments as needed and specified by management.Requirements for the role include: Bachelor’s degree in a relevant discipline and a minimum of 2-4 years of progressively responsible Regulatory Affairs experience in a pharmaceutical, biotechnology, contract research organization(CRO) or related environment with a preference for at least 1 year of successful experience in a European Regulatory Affairs role.Prior experience helping to build a regional Regulatory Affairs function for a growing organization.In-depth knowledge of relevant, regional regulatory guidelines and requirements.Demonstrated, hands-on experience managing and preparing all phases of regional/country- specific regulatory submissions including knowledge of registration procedures in Europe,Switzerland and UK, and in particular with the centralized procedure.Demonstrated track record of success building relationships with, and influencing, regional and/or national health authorities, particularly in situations requiring direct interaction/negotiation.Demonstrated success gaining regional regulatory approval and in providing regulatory support for post-marketing and life cycle management activities such as variations, renewals and labelling, aswell as for development activities, such as clinical trial applications.EEO Statement: PTC Therapeutics is an equal opportunity employer. We welcome applications from all individuals, regardless of race, color, national origin, gender, age, physical characteristics, social origin, disability, religion, family status, pregnancy, sexual orientation, gender identity, gender expression, disability, veteran status or any unlawful criterion under applicable law. We are committed to treating all applicants fairly and avoiding discrimination.Click here to return to the careers page