R&D activities:Operability of national, European and large-scale industrial projects focused on the evaluation of the fulfilment of legislative obligations related to under-development technologies and products from different sectors of use, including:• Substitution of substances subject to authorization or restriction and impact on the industrial processes.• Evaluation of the risks posed to human health (occupational and/or consumer) and the environment due to the use of the… Show more R&D activities:Operability of national, European and large-scale industrial projects focused on the evaluation of the fulfilment of legislative obligations related to under-development technologies and products from different sectors of use, including:• Substitution of substances subject to authorization or restriction and impact on the industrial processes.• Evaluation of the risks posed to human health (occupational and/or consumer) and the environment due to the use of the chemical compounds in different applications.• Exploring alternative testing methodologies and improvement of in silico methods of testing (QSAR tools).• Collection of information from EU Authorities databases (ECHA, EFSA, EMA) regarding hazard characterisation of chemical compounds.• Use of specific tools (GUIDEnano, Stoffenmanager®, Advance REACH Tool, ECETOC TRA, ConsExpo, EUSES) for the determination of exposure levels of chemicals at the different stages of the life cycle.• Revision of criteria on hazardous substances to be implemented in EU Ecolabel schemes and comparison with other ecolabel schemes (Blue Angel, Austrian Ecolabel, Nordic Swan).• Organising workshops for the engagement of relevant stakeholders with regards to different legislative frameworks.Compliance services:Support to assess how a company is impacted by sector-specific regulations and voluntary schemes (EU Ecolabel).• Legislative assessment: detailed in-company assessment of the degree of impact of relevant EU legislative texts on the company.• Action plans to comply with the applicable legislation of the sector of use.• Preparation of registration dossiers and notifications to substances subject to authorisation.• Interpretation of legal texts and guidance.• Elaboration of regulatory documentation (e.g., SDS).• Training and educational services, tailored to the needs of the company on legislative compliance, (nano)materials characterisation and risk assessment. Show less

Regulatory Affairs:- Consulting Business Unit and Product Manager in regards of all chemical legislations.- Managing and maintaining Regulatory related documents for all company products (SDS, Certificates, etc.).- Coordinating hired external services in regards to relevant product documentation (SDS, Certificates, etc.).- Ensuring legal compliance with all relevant European and local Regulations for all company products (before products can… Show more Regulatory Affairs:- Consulting Business Unit and Product Manager in regards of all chemical legislations.- Managing and maintaining Regulatory related documents for all company products (SDS, Certificates, etc.).- Coordinating hired external services in regards to relevant product documentation (SDS, Certificates, etc.).- Ensuring legal compliance with all relevant European and local Regulations for all company products (before products can be sold).- Registration of substances at European and local Authorities (REACH, CLP, Biocides, etc.).- Notification of substances at European and local Authorities (Nanoparticles, ChemVerbotsV, etc.).- Communication with Only Representatives to ensure legal compliance of non-EU products.- Administrating and implementing new and relevant Laws and Regulations on a company level, if applicable.- Conducting internal Trainings for all European colleagues regarding Regulatory Affairs and Quality Management.- Fulfilling necessary Regulatory and Quality questionnaires from customers.- Content Manager of relevant Regulatory Affairs internal communication. Quality Management: - Quality Management Representative during External audits.- Conducting internal audits company wide as lead auditor.- Conducting internal audits company wide as second auditor.- Documentation and follow-up of conducted audits.- Administrating and implementing the new requirements of ISO 9001:2015 and ISO 14001:2015 company wide.- Content Manager of relevant Quality Management internal communication. Show less

- Homologation of pigments for pigment bases of water and solvent based inks.- Development of new formulations.

- Development of IT applications / programs of the company.- Technical support to the different departments.

- Assistant in the development of new biopolymers for medical applications.