Quality Assurance Expert Compliance, Drug Product Services (m/f/d) in Basel

veröffentlicht
Kontakt
Mari Slavova, Randstad Inhouse Services Lonza Visp
Jobtyp
Temporär
jetzt bewerben

job details

veröffentlicht
Ort
Basel, Basel-Stadt
Sektor
Life Sciences
Jobtyp
Temporär
Referenznummer
142523-1147
Kontakt
Mari Slavova, Randstad Inhouse Services Lonza Visp
Telefon
+41 61 316 25 42

Stellenbeschreibung

We are looking for a Quality Assurance Expert Compliance, Drug Product Services (m/f/d) for Lonza AG (100%). This is a temporary position for 8 months, with an opportunity to extend.

Today, Lonza is a global leader in life sciences operating across three continents. While Lonza works in science, there's no magic formula to how they do it. Their greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, they let their people own their careers. Their ideas, big and small, genuinely improve the world. And that's the kind of work Lonza wants to be part of.

Key responsibilities:

  • Ensures the proper qualification of supplier/material/services by supervising adherence to quality agreements and audit observations

    • Tracking and follow up of supplier audit status and CAPAs including linked material

    • Tracking GMP status of service providers (e.g. calibration, maintenance, consultants)

    • Tracking GMP status of equipment/instruments/computerized systems

    • Supporting the global team for establishment of (supplier) quality agreements and keeping them up to date

  • Supports and executes GMP compliance activities like status reporting and trending of changes, non-conformities, CAPAS, Audits/Inspections, self-inspections, document management, vendor change notifications, local implementation of corporate documents

  • Supports establishment and maintenance of the Quality Management System at Drug Product Services (DPS) for QC and manufacturing plant

    • Supports DPS QA in creation of monthly and yearly quality reports

    • Supports DPS users in document life cycle management

  • Supports the groups in DPS in projects and GMP aspects.

  • Performs other duties as assigned.

Qualifikation

  • At least 3 years work experience in QA compliance/GMP area

  • Open minded, self driven, independent

  • Structured working attitude

  • Professional in English and German

  • Likes to work in an international team and intercultural environment

  • Agile to adopt to new situations and moving targets in short period of time