Oportunidades de Carreira

Quero candidatar-me

Development and validation of analytical methods for characterization of lipid-based nanoparticles (raw materials, in-process controls, intermediate products and drug product);
Compliance with GMP, ICH and other regulations in force and applicable to the development and validation of analytical methods;
Resolution of analytical, technical and scientific problems;
Elaboration and verification of relevant documentation (analytical procedures, protocols and reports);
Active collaboration on internal dissemination of knowledge (including provide training, prepare presentations, and participate in discussion forums…).

Degree in Chemistry, Pharmaceutical Sciences, Biochemistry or similar;
Minimum of 2 years of experience of working in laboratory setting (quality control analysis or similar) – mandatory:
Experience in chromatographic techniques such as TLC, HPLC, GC-FID, HS-GC/FID, GC-MS, HS-GC/MS; LC-MS; HPLC-ELS, spectrophotometric techniques ( e.g., FTIR, UV), classical chemistry techniques (e.g., water content) and particle and solid state characterization techniques (microscopy, particle size determination, X-ray diffraction, etc,) – desirable;
Solid knowledge in nanoparticles and related characterization techniques – desirable;
Experience in development and validation of analytical methods – desirable;
Solid knowledge in quality control of sterile products – desirable;
Fluency in English (oral and written) – mandatory;
Good computer skills (Competent in Microsoft Word and Excel as a minimum);
Flexibility and adaptability to different analytical software;
Strong time management and organization skills;
Communication skills to develop good working relationships and to work effectively in a team environment;
Strong analysis and problem-solving skills;
Close attention to detail and high commitment to quality;
Be proactive and critical.

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