Quality Assurance Technician

SOLTI #cancerresearch; Albacete; Híbrido; EUR 25.000 - 45.000; A tiempo parcial

Descripción de la vacante

Ein innovatives Unternehmen im Bereich der klinischen Forschung sucht einen Quality Assurance Technician, der das Team unterstützt. In dieser spannenden Rolle sind Sie verantwortlich für die Qualitätssicherung in klinischen Studien, die Einhaltung der Datenschutzbestimmungen und die Unterstützung bei Audits. Das Unternehmen bietet eine flexible Arbeitsumgebung, kontinuierliche Weiterbildung und echte Karrierechancen. Wenn Sie detailorientiert sind und eine Leidenschaft für Forschung haben, ist dies die perfekte Gelegenheit für Sie.

Servicios

Flexible Arbeitszeiten

Fortbildungsmöglichkeiten

Karrierechancen

Wettbewerbsfähige Vergütung

Formación

• Erfahrung in der Qualitätssicherung in klinischen Studien.
• Kenntnisse in ISO 9001 sind von Vorteil.

Responsabilidades

• Überwachung der Trial Master File (TMF) zur Gewährleistung der Integrität.
• Mitwirkung an internen und externen Audits.

Conocimientos

Qualitätssicherung

GCP Erfahrung

Microsoft Office

Detailorientierung

Kommunikationsfähigkeiten

Educación

Bachelor in Lebenswissenschaften

Descripción del empleo

SOLTI is an academic research group that performs clinical trials of excellence in oncology. Currently, SOLTI is comprised of over 550 renowned research professionals distributed over a broad network of more than 100 leading hospitals in Spain, Portugal, France and Ireland.

SOLTI focuses its efforts on developing cutting-edge clinical trials with novel targeted therapeutics including innovative translational research, fostering the participation in international networks and promoting excellence in the management of cancer among their members.

We are currently seeking a Quality Assurance Technician to join our Quality Department and support key initiatives in clinical research and environmental sustainability .

Location : Barcelona (hybrid working model)

Schedule : Part-time (20h / week) with the possibility of transitioning to full-time in the near future.

Main responsibilities :

• Quality Control in Clinical Trials : Supervise the Trial Master File (TMF) to ensure its integrity and regulatory compliance.
• GDPR Compliance : Manage documentation related to data protection.
• Vendor and Client Relations : Support the management of quality-related surveys and evaluations.
• Document Management : Contribute to reviewing, drafting, and controlling quality system procedures and documents.
• Audits : Assist in the preparation and execution of internal and external audits.
• Sustainability : Actively participate in implementing our Corporate Sustainability Plan with an environmental focus.

We are looking for :

• A bachelor’s degree in Life Sciences (mandatory).
• Previous experience in Quality Assurance within clinical research. Familiarity with ISO 9001 is a plus.
• GCP experience.
• Advanced proficiency in Microsoft Office tools.
• Proactive, detail-oriented, and methodical approach.
• Strong communication skills and a team player.
• High adaptability and ability to collaborate across multiple departments.
• Integrity and professionalism in handling sensitive documentation.

What we offer :

• A leading environment in clinical research.
• Continuous training and professional development , with company-funded learning opportunities.
• Flexible working hours and work-life balance.
• Real opportunities for career progression.
• Competitive compensation , aligned with your experience and profile.
• Immediate start and onboarding from day one.

If you believe you possess the qualifications for this position, we want to hear from you!

SOLTI is an employer committed to Equal Opportunities regardless of sex, gender, sexual orientation, race, age, origin or disability.

Get to know us at :

JobOpening #QualityAssurance #ClinicalTrials #ResearchJobs #OncologyResearch #LifeSciencesCareers #SOLTI #NowHiring