Overview:
**Responsibilities**:
1. Hands on the use of differenet analytical methods (TGA; DSC; GPC; Rheometer, GS-MS; HPLC-MS; ICP-OS).
2. The analyst will be involved in the organization and performance of medical devices /drug products extractables and leachables work plans, data collection, compatibility assessment and analysis, including nitrosamines product evaluation.
3. Interpretation of the data associated with each analysis (polymers and finished product) as well as the documentation of research reports validations of analytical methods to ensure correct performance of the test in accordance with GMP standards
4. Interpretation of analytical results, drawing conclusions and lines of action. Preparation of presentations and reports results. Writing and review reports and GMP laboratory documentation (analytical development methods/reports).
5. Strong problem solver who is highly organized with the ability to thrive and to lead in an environment with rapidly changing priorities
Qualifications:
- **Education**:Bachelor´s degree in sciences (Pharmacy, Chemistry, Biochemistry).
- ** Languages**: High level of Spanish and medium/high level of English.
- ** Experience (years/area)**: Minimum 1 years’ experience as an analyst, scientist, or technician in an analytical environment (Pharma industry).
- ** Specific Knowledge**: GMP regulations.
- ** Travels**:Not required.
- ** Personal skills**
Good scientific, technical, analytical, and problem-solving skills, with the ability to design experiments and interpret data independently.
Experience on working in a GMP environment.
Enthusiastic and hard-working individual who enjoys working as part of a team.
Self-motivated with ability to independently progress work projects.
Willingness to work in an interdisciplinary environment.
Excellent written and verbal communication skills in both English and Spanish