Damien C. Email and Phone Number

In charge of a team dedicated to the Research and the Development of New PET Tracers for the group (Transversal function with RA and QA teams; Legal and IP departments; Production sites managers and Marketing):- Establish Department Strategy (Develop Capacities, P&O, Business plans, Technical feasibility of projects, Research trends, etc.) for PET tracers from early Research to Transfer to market - Project management of chemical Precursors, DS and DP (Development plan, Risk assessment, Rationalisation of choices) - People management - Definition and proposition of the sourcing strategy - Lead of contract negotiations with CMOs - Review of Quality/Technical agreements and Manufacturing/Supply contracts with QA Manager and Legal Department

In charge of a team dedicated to new APIs for all development activities of the group (Transversal function with R&D, RA and QA teams; Legal and IP departments; Production sites managers and Marketing): - Project management of DS (Development plan, Risk assessment, Rationalisation of choices) - Definition and proposition of the API sourcing strategy; development of a qualification/validation method for the assessment of suppliers (organic compound, biomolecules…) at corporate level - Lead of contract negotiations with CMOs for API supply and cGMP manufacturing - Review of Quality/Technical agreements and Manufacturing/Supply contracts with QA Manager and Legal Department - Collaboration with RA department to assess the product characteristics and stability programs for API. Interaction with the suppliers to insure the ASMF/DMF is online with current regulations and in line with the development phases of the pharmaceutical (phases I, II, III or market) - Responsibility for the accuracy and reliability of the information generated in the drug development programs, including API stability testing programs. - Setting-up of budget and follow-up for all the API in development - Work in collaboration with radiopharmaceutical product development team (ready-to-use injectable solutions and kits for radiopharmaceutical preparation)- Technical support of QA Corporate Manager during audits, change control and/or assessment of deviations on qualityTo develop R&D projects and assess new technology: - Take part in the assessment of initiatives and partnership as technical support; - Evaluation of technology in Due Diligence - Suggest, develop and assess new R&D projects To take part of commercial launch of a new product: - Technical support for hospitals and sales team - Develop and assess appropriate documentation to support commercialization - Evaluation of customer complaints and put in relief potential improvements on products

- 68Ge/68Ga radionuclide generator assembly and study (long-lived radionuclide manipulation). Purification study and long-term quality monitoring of 68Ga- Development of several radioactive tracers (68Ga, 18F, 11C) from drug design to automated production followed by preclinical assessment.

Laboratoire d’Hétérochimie Fondamentale et Appliquée (LHFA), University, Toulouse 3French Armament Procurement Agency (DGA)French Armed Forces Biomedical Research Institute (IRBA-CRSSA), Grenoble - La Tronche- Synthesis, characterization and in vitro and in vivo evaluations of new organic and organometallic derivatives against damages caused by X- and g-rays (Chemical radioprotection).- 2007: Animal experiment agreement (level 2)

Organic compound development (Oxindoles)

Organic compound development (Indoles)

QC technician in pharmaceutical industry

Nuclear Physics Research in Mass Spectrometry (Trainee)