PRR Project
Principal Researcher in Pharmaceutical Nanotechnology
Project sheet
Name
Principal Researcher in Pharmaceutical NanotechnologyTotal project amount
95,41 thousand €Amount paid
95,41 thousand €Non-refundable funding
95,41 thousand €Loan funding
0 €Start date
20.06.2025Expected end date
31.03.2026Dimension
ResilienceComponent
Qualifications and SkillsInvestment
Science Plus TrainingOperation code
02/C06-i06/2024.P2023.15190.TENURE.007Summary
Job DescriptionThe employee is expected to:Carry out research activities, participate in the design, coordinate, develop and translate research programmes and projects within the scientific area, particularly in pharmaceutical biotechnology and pharmaceutical nanotechnology, nanomedicines, drug delivery systems and drug targeting. These tasks involve the development and characterization of pharmaceutical products (including in vitro and in vivo evaluation), scale-up and technology transfer. He/she is also expected to attract international and national competitive funding.Coordinate research teams, supervise and participate in training programmes of the institution, develop training activities within the scope of the methodology of scientific research and development, including scientific orientation of students, particularly of doctoral and master´s supervisions in the scientific area (pharmaceutical biotechnology and pharmaceutical nanotechnology, nanomedicines, drug delivery systems and drug targeting, development and characterization of pharmaceutical products).Intervene in the scientific community, showing autonomy and leadership, coordinate and participate in initiatives to create or strengthen laboratory infrastructures to support research. ??????? Scientific ProfileThe candidate should demonstrate proficiency in the development and in vitro/ in vivo evaluation of micro/nanoparticulate systems for effective drug delivery including drug stabilization, co-delivery and targeting, particularly for biological drugs, such as proteins, nucleic acids and antigens for vaccine formulation. Relevance is given to drug and vaccine delivery using non-parenteral routes, such as ocular, oral, pulmonary and intranasal, for improving bioavailability. This includes the modulation of antigen presentation through mucosal immunisation using nanovaccine formulations with enhanced mucoadhesive properties, aiming oral, buccal and intranasal delivery. In this context, the employee should have a solid pharmaceutical biotechnology background, including cell technology, recombinant protein and antigen production, purification and characterization under Good Laboratory Practice (GLP) for scale-up and technology transfer. RationalePharmaceutical Sciences are the main scientific area of any Faculty of Pharmacy. Within this area, the position is aligned with the scientific area of Pharmaceutics and Pharmaceutical Technology, which deals with the transformation of bioactive substances and excipients to obtain medicines and health products (e.g. cosmetics, nutraceuticals and medical devices) available in pharmaceutical dosage forms, ensuring that these preparations are endowed with maximum activity, dosed with the greatest precision and presented in a form that facilitates their preservation and administration. It involves the design, formulation and delivery of drugs, the technological processes of drug preparation on a laboratory or industrial scale, as well as their stability, control and quality assurance. It includes the technological and biological foundations, strategies and applications of drug vectorization and molecular therapeutics.During the last three decades, at FFUL this scientific area, has consistently grown and evolved in line with the latest scientific advances in the field of drug delivery and targeting, which is demonstrated by the preeminent scientific production record of the four research groups of the area in iMed.ULisboa (i.e., the Advanced Technologies for Drug Delivery , the Drug Delivery & Immunoengineering , the Pharmaceutical Development and the Pharmaceutical Manufacturing and Engineering research groups). The research work developed by these groups is focused drug development, manufacturing and delivery related to oncological, genetic, neurodegenerative and infectious diseases, as well as the development of personalized medicine. The most recent scientific breakthroughs in these diseases suggest, or have resulted in, biologic products whose market size is steadily increasing, accounting for ca. 430 billion € in 2022. This has also markedly increased the number of national and international research projects involving biologicals and vaccines, with competitive funding or research contracts with the industry, which are currently under development at iMed.ULisboa and need to be duly developed. Thus, the need for mature researchers with a sound biotechnological background to accomplish such commitments.
Beneficiaries
The two types are::
- Direct Beneficiaries are those whose funding and projects to implement are part of the Recovery and Resilience Plan that has been negotiated and approved by the European Union;
- Final Beneficiaries are those whose funding and projects to implement are approved following a selection process through Calls for Applications.
Call for applications
As part of the Call for Applications, submissions are requested to select the projects and final beneficiaries to whom funding will be awarded. Specific selection criteria are defined for each call, which must be reflected in the applications submitted and assessed.
The project is appraised on the basis of its compliance with the selection criteria laid down in the calls for applications, and a final score may be awarded, where applicable.
Final evaluation score
The components for calculating the assessment score can be found in the selection criteria document mentioned below.
Selection criteria
Beneficiaries
Intermediate beneficiaries
Procurement
Beneficiaries representing public entities implement their project by signing one or more contracts with suppliers for goods or services through public procurement procedures.
To ensure and provide the utmost transparency in all these contracts, a list of the contracts that were signed under this project is available here, along with the information available on the Base.Gov platform. Please note that, according to the legislation in force at the time the contract was signed, some exceptions do not require the publication of the contracts signed on this platform, and, therefore, no information is available in such cases.
Geographic distribution
95,41 thousand €
Total amount of the project
Percentage of the amount already paid for implementing projects
, 100 %,Where was the money spent
By county
1 county financed .
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Lisboa 95,41 thousand € ,