Role Description En tant qu'adjoint(e) à la cheffe d'unité, vous aurez comme missions principales d'assurer le suivi et la mise en oeuvre des conventions ANRU et vous participerez ainsi à la transformation des quartiers objets de ces interventions. - Accompagner le responsable de l'unité dans ses missions de coordination et de pilotage de la cellule pour pouvoir assurer sa suppléance en disposant d'une vision globale des différents dossiers. - Porter les priorités de l'ANRU et de ses partenaires en appuyant les collectivités dans l'élaboration des documents contractuels et le suivi des études, en élaborant les avis de l'État et en préparant les différentes réunions de pilotage. - Assurer le suivi des documents contractuels en vue de leur présentation à l'ANRU et suivre les dispositifs permettant la pérennisation des investissements. - Instruire et contrôler les dossiers de subvention transmis à la signature du délégué territorial de l'ANRU. Qualifications - Poste de catégorie B (administratif ou technique) - Aisance relationnelle - Très bonne compréhension des politiques publiques de l'habitat social et des actions portées par l'ANRU - Familiarité avec le montage opérationnel et financier d'opérations pluri-annuelles complexes - Connaissances sur les missions du ministère de l'écologie et le fonctionnement des directions interministérielles et de l'ANRU (un plus) Elements de candidature - Documents à transmettre : CV et lettre de motivation sont obligatoires Contact - Email : sophie.navarre@marne.gouv.fr - Email : david.dealisse@marne.gouv.fr

Regulatory Associate (EU mkt, CMC module 3) Syneos Health® is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the drug development and commercialization continuum, helping them navigate complexity, anticipate change and accelerate progress. Our Clinical Solutions team members act with a drug development mindset, applying their years of experience and deep expertise to truly understand customer needs and represent those in the solutions we shape. Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you’ll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to deliver – for one another, our customers, and, most importantly, for those in need. Discover what your 25,000 future colleagues already know: Why Syneos Health • We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program. • We are committed to building an inclusive culture – where you can authentically be yourself. Central to this is our purpose – Driven to Deliver – which captures the passion of our colleagues to show up each day and shape solutions that have the ability to dramatically impact someone’s life. • We are continuously building the company we all want to work for and our customers want to work with. Why? Because we know that when we bring together smart colleagues from across the world, we can shape the future of healthcare, driving impact for customers and defining the pace of patient progress. Job Responsibilities JOB RESPONSIBILITIES - Should have minimum 6 months to 2 years of experience - Candidates with internship preferred - Should have CMC experience in small molecule. - Markets experience in EU, GCC, APAC would be preferred - Essential Functions - Assists with preparation of product development documents including gap analyses and clinical development plans. - Assists with preparation of regulatory submission documents including components of investigational new drug applications (INDs), new drug applications or new marketing applications (NDAs/MAAs), drug master files (DMFs), variations, renewals, marketing authorisation transfers (MATs) and other lifecycle maintenance activities, according to current government regulations and guidelines. - Conducts regulatory research to identify regulatory precedents and to support the preparation of orphan drug designation requests. - Performs quality checks on related documents. - Assists with submissions of other regulatory documents and other regulatory research as needed. - Assists clients, customers, or others with general information - Gathers, compiles, analyzes, and reports information. - Gathers information, searches files and records, and makes personal contacts to obtain specific information in order to prepare detailed reports and compose routine correspondence. QUALIFICATION REQUIREMENTS - Excellent interpersonal / communication skills. - Advanced skills in Microsoft Office Applications. - Good time and project management skills, preferred. - Strong analytical skills and attention to detail. - Ability to work both as a team member and independently and to understand and carry out detailed instructions. - Ability to interact with staff from multiple departments. - Ability to work concurrently on projects, each with specific instructions that may differ from project to project preferred. - Fluent in speaking, writing, and reading English. Get to know Syneos Health Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000+ Trial patients. No matter what your role is, you’ll take the initiative and challenge the status quo with us in a highly competitive and ever-changing environment. Learn more about Syneos Health. http://www.syneoshealth.com Additional Information Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job.

Role Description Au sein de l'unité politique sociale du logement, vous êtes chargé(e) de piloter et animer l'unité, de garantir le rôle de l'État dans la gestion locale des attributions et coordonner l'ensemble des réflexions en matière d'accès au logement social sur le territoire, de mettre en oeuvre les politiques sociales du logement en lien avec la DEETS : la prévention des expulsions locatives, le relogement des publics prioritaires, le DALO. Vous effectuez ces missions en veillant au respect des délais d'instruction et des procédures. Vos actions contribuent à la lutte contre l'exclusion sociale. - Piloter et animer l'équipe, afin de contribuer à la cohésion de l'unité PSL; - Élaborer, mettre en oeuvre et coordonner le plan territorial d'action pour le logement et l'hébergement des personnes défavorisées (PTALHPD), en lien avec la CTM; - Mettre en oeuvre les politiques sociales du logement et les réformes y afférentes; - Veiller à la mise en oeuvre du droit au logement; - Piloter l'unité dans les domaines de l'attribution des logements sociaux (contingent de l'État), du DALO et de la prévention des expulsions locatives; - Veiller à la qualité de l'accueil du public (téléphonique et physique); - Assurer le suivi des activités des bailleurs en matière d'attribution de logements (gestion en flux); - Accompagner les collectivités dans l'élaboration des Conférences Intercommunales du Logement (CIL) et des plans partenariaux de la gestion de la demande; - Coordonner et animer la CCAPEX; - Représenter la DEAL aux différentes réunions; - Veiller à la production des tableaux de bord et des statistiques de l'unité. Qualifications - Connaissance de l'environnement professionnel, notamment celui du service et des acteurs du logement; - Connaissance des politiques locales de l'habitat et des politiques sociales du logement; - Connaissances juridiques de base; - Connaissance de la réglementation relative au DALO et à la PEX; - Connaître les techniques d'accueil du public; - Maîtriser les outils bureautiques. Requirements - Savoir manager; - Savoir animer une réunion, un réseau; - Savoir rédiger des courriers et des PV de réunion; - Avoir l'esprit de synthèse, d'analyse et être force de proposition; - Faire preuve de rigueur et de méthode; - Faire preuve de capacité d'initiative, d'adaptation et de réactivité; - Être autonome; - Savoir respecter les délais; - Faire preuve de rigueur et de méthode. Benefits - Savoir travailler en équipe; - Savoir accueillir, écouter et communiquer avec amabilité et courtoisie; - Faire preuve de discrétion et de disponibilité; - Avoir le sens et le goût du contact; - Savoir s'exprimer à l'oral devant un public; - Être à l'écoute; - Obligation de discrétion et de confidentialité. Éléments de candidature - Documents à transmettre : Pour postuler à cette offre, l'envoi du CV et d'une lettre de motivation est obligatoire; - Personnes à contacter : bernard.planchet@developpement-durable.gouv.fr, cyrille.liroy@developpement-durable.gouv.fr.

Senior Regulatory Affairs Specialist Location: Sarasota, FL; Charlotte, NC; Milford, DE; or York, PA, United States Job Description: Company: Dentsply Sirona, Inc Dentsply Sirona is the world's largest manufacturer of professional dental products and technologies, with a 130-year history of innovation and service to the dental industry and patients worldwide. Dentsply Sirona develops, manufactures, and markets a comprehensive solutions offering including dental and oral health products as well as other consumable medical devices under a strong portfolio of world class brands. Dentsply Sirona's products provide innovative, high-quality and effective solutions to advance patient care and deliver better and safer dentistry. Dentsply Sirona's global headquarters is located in Charlotte, North Carolina. The company's shares are listed in the United States on NASDAQ under the symbol XRAY. Bringing out the best in people As advanced as dentistry is today, we are dedicated to making it even better. Our people have a passion for innovation and are committed to applying it to improve dental care. We live and breathe high performance, working as one global team, bringing out the best in each other for the benefit of dental patients, and the professionals who serve them. If you want to grow and develop as a part of a team that is shaping an industry, then we're looking for the best to join us. Working at Dentsply Sirona you are able to: Develop faster - with our commitment to the best professional development. Perform better - as part of a high-performance, empowering culture. Shape an industry - with a market leader that continues to drive innovation. Make a difference -by helping improve oral health worldwide. This position can be a hybrid working arrangement for someone that is near one of the following Dentsply Sirona locations: Sarasota, FL; Charlotte, NC; Milford, DE; or York, PA. Job Summary: The Senior Regulatory Specialist is a contributing member of cross-functional teams in support of regulatory market access activities for US, Canada, EU, and other countries. May support NPD and Sustaining activities for the US, Canada and EU markets. Also supports additional international registrations. Key Responsibilities: - Assists in development and execution of regulatory strategies to obtain and maintain regulatory approvals for medical devices - Prepares and submits international regulatory submissions to obtain and maintain regulatory approvals for medical devices, including 510(k) submissions and technical files for CE Marking - Maintains regulatory files and databases to ensure compliance with regulatory requirements - Provides regulatory guidance and support to cross-functional teams throughout the product lifecycle - Participates in review of labelling and claims for the US and EU markets. - Reviews and interprets regulatory requirements and guidance documents to ensure compliance - Coordinates regulatory activities with internal teams and external regulatory agencies - Supports regulatory audits and inspections as SME for questions related to market access - Stays current with regulatory requirements and updates affecting medical devices - Fosters professional interactions with internal and external stakeholders through various communication channels, enhancing business relationships - Complies with company and departmental policies and administrative requirements - Performs other duties as assigned or as needed Education: - Bachelor's degree in a relevant field, such as life sciences, regulatory affairs, or a related discipline Years and Type of Experience: - 5(+) years of experience in regulatory affairs, preferably in the medical device industry - Experience with leading regulatory submissions and documentation, including 510(k) submissions and CE marking - In-depth knowledge of FDA regulations and international standards (e.g., ISO 13485, MDSAP, EU MDR) Required Computer / Software Skills: - Proficiency with Microsoft Office Suite - Proficiency with Regulatory software Key Required Skills, Knowledge, and Capabilities: - Strong attention to detail and organizational skills - Excellent communication (both written and verbal) and interpersonal skills - Ability to work effectively in a team environment - Knowledge of regulatory affairs principles and practices - Ability to critically review detailed scientific information and assess whether technical arguments are presented clearly, and conclusions are adequately supported - Willingness to learn and adapt to new processes and technologies - Regulatory registration experience within med device organizations - Prior technical writing experience and proven track record with FDA and EU regulatory submissions preferred. Dentsply Sirona is an Equal Opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, sexual orientation, disability, or protected Veteran status. We appreciate your interest in Dentsply Sirona. For California Residents: We may collect the following categories of personal information in connection with the submission of your resume or application materials to us for employment, and if hired, your employment with us: identifiers (e.g., name, address, email address, birthdate); personal records (e.g., telephone number, signature, education information, criminal background information, passport number and visa information); consumer characteristics (e.g., sex, marital status, veteran status, race, disability, sexual orientation); professional or employment information (e.g., resume, cover letter, employment history, background check forms, references, certifications, transcripts and languages spoken); and inferences from personal information collected (e.g., a profile reflecting abilities and aptitudes). The above categories of personal information are collected for the following business purposes: performing recruitment and hiring services; processing interactions and transactions (e.g., to comply with federal and state laws requiring us to maintain certain records, managing the workforce); and security (e.g., detecting security incidents, protecting against fraudulent or illegal activity).