Auditor in the Quality Assurance Unit (QAU)

Anapharm Bioanalytics; Barcelona; Presencial; EUR 30.000 - 50.000; Jornada completa

Descripción de la vacante

A growing biotechnology company in Barcelona seeks a professional to conduct internal audits, manage corrective actions, and prepare documentation of their Quality System. Candidates should hold a BSc or MSc in life sciences and ideally have experience with GLP and GCP regulations. Strong organizational skills and fluency in English are essential. The role offers career growth in a solid scientific team within a diverse environment.

Servicios

Opportunity to work in a growing CRO

Career growth opportunities

International work environment

Professional organization with a human touch

Formación

• Experience working under GLP and GCP regulations.
• Knowledge of bioanalytical techniques (LBA, LC-MS/MS) valued.

Responsabilidades

• Conduct internal audits according to GCP and GLP regulations.
• Manage and execute corrective and preventive actions (CAPA).
• Prepare documentation of Quality System (SOPs, forms, training records).
• Participate in validation of computerized systems.
• Support QAU Director in implementing new processes.

Conocimientos

Fluent written and spoken English

Good organizational skills

High attention to detail

Ability to work autonomously

Ability to work as part of a team

Educación

BSc or MSc in life sciences

Herramientas

MS-Office

Descripción del empleo

MAIN DUTIES & RESPONSIBILITIES

• Conduct internal audits (both study specific and Quality System related) and coordinate inspections by external auditors, according to GCP and GLP regulations.
• Manage and execute corrective and preventive actions (CAPA).
• Prepare and organize documentation of Quality System (SOPs, forms, training records, etc.).
• Participate in the validation of computerized systems.
• Actively support QAU Director in evaluating and implementing new department and Company processes.

REQUIRED PROFILE & QUALIFICATIONS

• BSc or MSc in life sciences.
• Experience working under GLP and GCP regulations will be greatly valued.
• Fluent written and spoken English.
• Proficiency in MS-Office, especially Word and Excel.
• Knowledge of bioanalytical techniques (LBA, LC-MS / MS) will also be valued.

OTHER REQUIRED SKILLS

• Good organizational skills and high attention to detail, with the ability to handle multiple tasks effectively and efficiently.
• Ability to work both autonomously and as part of a team, as required.
• High level of motivation.

WHAT IS OFFERED

• Opportunity to work and contribute to the success of an expanding CRO and a growing team.
• Solid scientific and QA teams with career growth opportunities.
• International and multicultural environment in company based in Barcelona.
• Diligent, professional organization, with a human touch.