- Revision of analytical results of raw material and finished product- Stabilities study revision- Release raw material, intermediate products and packaging- OOS/OOE and deviation investigation- CAPAs implementation- Calibration/verification equipment revision - Management of working standards and reagents- Deputy Laboratory Coordinator- Coordination with supply and production departments according to plant priorities - Projects management

- General and HPLC/GC analysis of stabilities, finished product, raw material and packaging- Equipment calibration/verification

- Responsible for shelf life test, microbiological trials, challenge testing and internal investigations- Coordinate and train of new staff, especially in counting area - Responsible for IQC and EQA - Ensure staff implement activities in accordance with SOP’s, Methods, Documents and Proformas and, in consequence maximise the work efficiency by implementing and encouraging communication between staff at all levels - Demonstrations with UKAS, Tesco, M&S audits and support with the… Show more - Responsible for shelf life test, microbiological trials, challenge testing and internal investigations- Coordinate and train of new staff, especially in counting area - Responsible for IQC and EQA - Ensure staff implement activities in accordance with SOP’s, Methods, Documents and Proformas and, in consequence maximise the work efficiency by implementing and encouraging communication between staff at all levels - Demonstrations with UKAS, Tesco, M&S audits and support with the closure of actions Show less

- Immersed myself within a research project, working independently applying the knowledge acquired during the years of biotechnology degree.- Focusing in the development of the CE, especially cIEF methods for the characterization of biopharmaceutical as mAb, ADC and EPO.- Overview of several methods and discussing data by weekly meeting of all the department members.- Worked in a high qualified environment with a competitive bonus culture for over 6 months.- Improving my… Show more - Immersed myself within a research project, working independently applying the knowledge acquired during the years of biotechnology degree.- Focusing in the development of the CE, especially cIEF methods for the characterization of biopharmaceutical as mAb, ADC and EPO.- Overview of several methods and discussing data by weekly meeting of all the department members.- Worked in a high qualified environment with a competitive bonus culture for over 6 months.- Improving my personal and professional skills as a team work member, communication skills, presentation skills and acquiring more confidence to lead whole project. Show less

- Performance of the usual quality control test of samples during all the bioremediation progress (pH, temperature, conductivity, DQO, DBO, TKN, alkalinity, nitrites and nitrates).- Control of MFC.- Update database required to do quality control test.

- Synthesis of antimicrobial cyclic peptides in solid phase by traditional process.- Analysis and identification of the peptides by HPLC and MALDI-TOF. - Troubleshooting of HPLC.- Data analysis.