Como se candidatar?
Para se candidatar a esta oferta de emprego, envie um email com a referência - Ref. 1332 - e com o seu Curriculum Vitae (CV) para recrutamento@bluepharma.pt.
Principais Responsabilidades
- Formulation and Process Development of complex formulations under QbD principles;
- Compliance with GMP, ICH and other regulations in force and applicable to the development and validation of drug products;
- Resolution of Technical and scientific problems;
- Plan and perform experiments, investigations and evaluations;
- Scaling up for manufacturing of batches for pre-clinical and clinical trials;
- Comprehensive reporting and documentation of results and experiments including development protocols and reports, following the internal procedures and current documentation practices;
- Support for necessary quality documentation for regulatory submissions;
- Active collaboration in internal dissemination of knowledge (including providing training, preparing presentations, and participating in discussion forums).
Requisitos
- Background in Chemistry, Pharmaceutical Sciences, Biophysics, Biochemistry or other related areas;
- A minimum of 2 years of experience and PhD is required;
- Knowledge of analytical techniques, namely principles and results interpretation, 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,);
- Fluency in English (oral and written);
- Knowledge of statistical concepts;
- Good computer skills (Microsoft Word, Excel and PowerPoint as a minimum);
- Strong time management and organization skills;
- Communication skills to develop good working relationships and to work effectively in a team environment;
- Strong analytical and problem-solving skills;
- Close attention to details and high commitment to quality;
- Be proactive and critical.
