MAIN DUTIES & RESPONSIBILITIES
1. Conduct internal audits (both study specific and Quality System related) and coordinate inspections by external auditors, according to GCP and GLP regulations.
2. Manage and execute corrective and preventive actions (CAPA).
3. Prepare and organize documentation of Quality System (SOPs, forms, training records, etc.).
4. Participate in the validation of computerized systems.
5. Actively support QAU Director in evaluating and implementing new department and Company processes.
REQUIRED PROFILE & QUALIFICATIONS
6. BSc or MSc in life sciences.
7. Experience working under GLP and GCP regulations will be greatly valued.
8. Fluent written and spoken English.
9. Proficiency in MS-Office, especially Word and Excel.
10. Knowledge of bioanalytical techniques (LBA, LC-MS/MS) will also be valued.
OTHER REQUIRED SKILLS
11. Good organizational skills and high attention to detail, with the ability to handle multiple tasks effectively and efficiently.
12. Ability to work both autonomously and as part of a team, as required.
13. High level of motivation.
WHAT IS OFFERED
14. Opportunity to work and contribute to the success of an expanding CRO and a growing team.
15. Solid scientific and QA teams with career growth opportunities.
16. International and multicultural environment in company based in Barcelona.
17. Diligent, professional organization, with a human touch.