· Entire business product portfolio was transferred from DuPont and integrated into IFF· Identify and leverage market opportunities for pharma products in food/supplements applications and vice versa, considering existing health claims and labeling assessment· Exploring regulatory paths for a food additive used and filed as an API (atypical active)· Address health concerns such as nitrosamines, nanoparticles, PFAS, MOAH, ETO and heavy metals both internally and through trade… Show more · Entire business product portfolio was transferred from DuPont and integrated into IFF· Identify and leverage market opportunities for pharma products in food/supplements applications and vice versa, considering existing health claims and labeling assessment· Exploring regulatory paths for a food additive used and filed as an API (atypical active)· Address health concerns such as nitrosamines, nanoparticles, PFAS, MOAH, ETO and heavy metals both internally and through trade associations, including a conference presentation on microplastics and their industry impact· Develop technical expertise and ensure knowledge transfer post-mergers with a comprehensive onboarding roadmap· Ensure data on food and feed additives is provided to EFSA and the EU Commission· Successfully advocated for the inclusion of specific differentiated Certification of Suitability (CEP) for excipients on EDQM’s agenda Show less

· Entire business product portfolio was transferred from Dow and integrated into DuPont· Responsible for regulatory compliance of the DuPont N&B business ($250M in EU annual revenue)- Follow EU-legislation to identify impact on business early and develop ways to reduce it- Assess products to ensure legal compliance with national/EU requirements of source and destination countries. If necessary, notify internally and/or externally· Responsible for novel product registrations in… Show more · Entire business product portfolio was transferred from Dow and integrated into DuPont· Responsible for regulatory compliance of the DuPont N&B business ($250M in EU annual revenue)- Follow EU-legislation to identify impact on business early and develop ways to reduce it- Assess products to ensure legal compliance with national/EU requirements of source and destination countries. If necessary, notify internally and/or externally· Responsible for novel product registrations in the European Union· Actively manage regulatory and toxicological data including IT management (SAP ERP)· Develop and keep cross-functional product stewardship business management system and processes working. Provide internal training on Product Stewardship when necessary· Identify dependencies (technical, regulatory, marketing, production process, transport and logistics) in a complex business environment· Answer internal and external inquiries on product safety issues for the DuPont N&B pharma, food, feed, supplements, medical device, personal care and industrial product lines· Advocate for and/or lead pharmaceutical, food, feed, supplements, medical device, personal care and industrial application initiatives of importance to DuPont as member and representative of DuPont in various Industry groups/associations:- Global cellulose trade association (OFCA, Vice-President position)- International Pharmaceutical Excipients Council Europe (IPEC EU)- Active Pharmaceutical Ingredients Committee (APIC, a sector group of CEFIC)- European Fine Chemicals Group (EFCG, a sector group of CEFIC)- EU Specialty Food Ingredients (EU SFI) Show less

• Responsible for regulatory compliance of the DFP&M business- Follow EU-legislation to identify impact on business early and develop ways to reduce it- Assess products to ensure legal compliance with national/EU requirements of source and destination countries. If necessary, notify internally and/or externally• Responsible for novel product registrations in the European Union• Actively manage regulatory and toxicological data including IT management• Develop and keep… Show more • Responsible for regulatory compliance of the DFP&M business- Follow EU-legislation to identify impact on business early and develop ways to reduce it- Assess products to ensure legal compliance with national/EU requirements of source and destination countries. If necessary, notify internally and/or externally• Responsible for novel product registrations in the European Union• Actively manage regulatory and toxicological data including IT management• Develop and keep cross-functional product stewardship business management system and processes working. Provide internal training on Product Stewardship when necessary• Ability to identify dependencies (technical, regulatory, marketing, production process, transport and logistics) in a complex business environment• Answer internal and external customer inquiries on product safety issues for the DFP&M pharma, food and industrial product lines• Advocates for and/or leads food and pharma initiatives of importance to Dow as member and representative of Dow in various Industry groups/associations: Technical Working Group of OFCA, IPEC Europe Harmonization Committee and ELC• Responsible for the conduct of Life-Cycle Assessments (LCA)• Also belongs to the Environment, Health & Safety (EH&S) Product Regulatory Services (PRS) Show less

Within the Environment, Health & Safety (EH&S) and Sustainability department, therole of this function is to harmonize the REACH registration models to cover Dowʼssubstances. REACH (Registration, Evaluation, Authorization of Chemicals) is theEuropean Union chemicals legislation

• Conducted market and sales analysis to define a new marketing strategy(1M EU potential patients representing potential annual revenue of $200M)• Creation of strategic tools and collateral material enabling therapy awareness and product solutions• Supported a product launch by gathering and analysing Voice Of Customer (VOC)• Event management, including booth design strategy, at two major European congresses(6’500 and 8’000 participants respectively)• Contributed in the… Show more • Conducted market and sales analysis to define a new marketing strategy(1M EU potential patients representing potential annual revenue of $200M)• Creation of strategic tools and collateral material enabling therapy awareness and product solutions• Supported a product launch by gathering and analysing Voice Of Customer (VOC)• Event management, including booth design strategy, at two major European congresses(6’500 and 8’000 participants respectively)• Contributed in the organization of the annual sales meeting, including key presentations(400 EU employees)• Prepared ad hoc reports and presentations to support the management and communication team,including marketing analysis of Key Metrics, Market Share and Market Penetration• Interviewed relevant stakeholders for promotional tool creation and consolidated data accordingly,presented the findings to the marketing team• Involved in the launch and implementation of a Customer Relation Management tool (CRM)(salesforce.com application deployed in 30 EU countries, 70 sales representatives) Show less

• Contribution to develop documentation for the student’s economic magazine association (interview writing and photograph).

• Coordination and provision of academic support to the departmental students• Monitoring library documentation

• Managerial training, responsible for the NBC detection service and military training of the company (over 200 people per annum)

• Created a study exploring maximum production capacity of novel cancer drugs based onmarine components (the study was part of the company’s annual Key Performance Objectives)• Gained knowledge of multiple elements involved within the life cycle of an oncological drug fromResearch and Development (R&D) to the market launch (world’s largest library of extracts from marine organisms – 200’000 extracts)

• Provision of administrative and managerial support to the association’s budget forecasting