Experience

ALDO-UNIÓN

• Spain
• Pharmaceutical Manufacturing
• 100 - 200 Employee

• Responsable I+D

  • Sep 2022 - Present



Nanopharm Ltd, an Aptar Pharma Company

• United Kingdom
• Pharmaceutical Manufacturing
• 1 - 100 Employee

• Head of Generics & Life-Cycle Management Pharmaceutical Development

  • Mar 2021 - Aug 2022

  - Establish strategies that meet project and regulatory requirements- Develop and maintain suitable project schedules, budgets and risk mitigation plans with project teams and external service providers- Liaise with service providers on a regular basis to monitor progress against milestones, as well as resolve technical, quality or resource issues smoothly- Review and manage technical data and documentation to ensure timely action, compliant storage and efficient retrieval- Bringing up to date knowledge and experience of developing formulations and processes and provide advice and best practice in this fast-moving research & development- Able to operate in a global process/project oriented environment with experience of QbD and technology transfer.- Responsible for staff within the department, recommending salaries and promotions.- Responsible for selecting and hiring people in co-operation with senior line management and HR.- Responsibility for safety and work environment for the group.- Authority to purchase goods and services and approve deliverables.- Appoints responsible persons for specific instruments/Equipment.- Responsible for availability of resources, monthly status reporting and performance of staff within the group.- Primary supervisor on development work, internal processes, external co-operations and scientific contacts.- Represent the department at internal and external meetings.

• Principal Scientist

  • Feb 2019 - Mar 2021

  - Lead, represent, manage and support the laboratory manufacture of small product batches for DPI, MDI and nasal spray.- Responsible for the product development, including external contact with third party company.- Contact with CROs/CDMOs managing different activities including formulation feasibility, scale up, tech transfer.- Design experimental protocols.- Good understanding of ICH, EMEA and FDA guidelines related to inhaled products development.- Organisation and scheduling of work and resources.- Writing, reviewing and approval of SOPs.- Writing of summary reports.

• Senior Scientist

  • Nov 2018 - Feb 2019

  - Research, design, manufacture and screen conventional and novel pMDI and DPI inhalation formulations and product concepts using a range of laboratory equipment and preparation techniques. - Conduct in-vitro data analysis and interpretation of data

• Pharmaceutical Analyst

  • May 2018 - Oct 2018

  - Conduct laboratory experiment including analytical method development, validation and method transfer. Primary techniques are HPLC - UV – ELSD, Aerodynamic particle size distribution by Next generation Impactor (NGI) and Andersen Cascade Impactor (ACI), Dosage Unit Sampling Apparatus (DUSA), Karl fisher for DPI and pMDI, formulation manufacture for DPI, pMDI and nasal spray, blend content uniformity, capsule content uniformity, droplet size distribution for nasal spray using the Spraytec (open bench), osmolality, surface tension, viscosity.- Theoretical knowledge of TGA, DSC, DVS,SEM, XRPD.



University of Parma

• Internship Student

  • May 2017 - Feb 2018

  Traineeship at Pharmaceutical Technology Laboratory and Drug delivery Traineeship at Pharmaceutical Technology Laboratory and Drug delivery