Beschreibung
Ihre Aufgaben
- Maintains document control system, including review, filing and archiving of data.
- Participates in the development and improvement of the management system.
- Trains staff or coordinates training in assigned department on Quality policies and procedures.
- Analyzes data, tracks / trends issues to identify gaps in processes, training, and helps create solutions through improvement process.
- Supports the quality managers with all quality system related topics (non-conformance, adverse events, corrective and preventive actions, change management)
- Coordinates closure of quality management system records (non- conformances, adverse events, changes etc…)
- Supervises all Quality practices and supports end-users to ensure high quality laboratory services.
- Keeps Quality Manager informed of any significant issues affecting overall laboratory quality including but not limited to audit findings, validations, corrective and preventative actions.
- Collects information for Annual Management Review (AMR), follow up on projects, objectives, manage AMR output (projects, tasks, action items); share data to relevant departments.
- Assists with internal audits. Performs audits in assigned laboratory and or department as directed.
- Supports/coordinates with quality managers complete and accurate readiness for all inspections and maintains all necessary documents.
- Participates in regulatory and accrediting agency inspections when needed
- Draft responses to regulatory inspection.
- Prepares filing for necessary licensure, certification and/or accreditation as appropriate for the laboratory's test complexity.
- Performs special projects as assigned.
- Actively participates as a member of the Quality Team.
Was Sie mitbringen
- Bachelor’s degree (or equivalent) in life science, medical laboratory science or quality
- Fluent in German and French, speaks professionally English
- Minimum 2 years of relevant experience in a Quality position within a life science industry
- Knowledge of ISO 15189, ISO17025 and IVDR (or ISO 13485)
- Good MS Office knowledge
- Good analytical and problem-solving skills.
- Good interpersonal skills.
- Good communication skills with ability to communicate with internal and external stakeholders.
- Good coordination and planning skills.
- Rigorous, organized and high level of attention to detail.
- Ability to work independently and initiate contacts as necessary.
- Good team player.
Was wir Ihnen bieten
- Ein spannendes und dynamisches Arbeitsumfeld mit viel Internationalität
- Übernahme von Verantwortung und die Entfaltung deines Potentials
- Ein positives Arbeitsklima mit einer partnerschaftlichen Zusammenarbeit und einer wertschätzenden und anerkennenden Firmenkultur
- Attraktive Fringe Benefits sowie eine 40h Woche und 5 Wochen Ferien
- Jahrespauschale für Ihre persönlichen Analysen und Spezialpreise für radiologische Beratung bei der Unilabs-Gruppe