CAPA Remediation Specialist

Genève  ‐ Vor Ort
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Schlagworte

Beschreibung

Our Global Medical Device client is looking for an experienced CAPA Remediation Specialist to support their compliance improvement project on site.
This role will be part of a wider quality improvement project being carried out across all QA work streams to drive regulatory compliance to an outstanding level.

Start: September 2014
Duration: 6-12 months
Location: Canton Zurich, Switzerland

Key Responsibilities:
Carry out full life cycle CAPA management and CAPA handling to close out deviations.
Write reports and documentation following internal templates.
Liaise with internal stakeholders.
Ensure all processes are GMP compliant.
Proactively examine CAPA systems, processes, and standards to identify areas for review, change, or elimination.
Analyse and report CAPA tracking and trending results and system performance metrics.

Requirements:
Degree educated with strong experience within the Medical Device and Pharmaceutical industry.
Experience working in a Manufacturing, Engineering, Quality Assurance or similar field in a regulated environment required.
Proven experience in CAPA management and CAPA handling.
Experience working with a CAPA system required.
In-depth knowledge of ISO and GMP requirements, with specific focus on CAPA required.
Excellent technical understanding.
Ability to work independently in a pressurised environment.
Strong analytical and problem-solving skills.
Excellent organisational, interpersonal, written and oral communication skills required.
Fluent German and English language skills.

Please apply now for this challenging, long-term position!
Start
keine Angabe
Von
Quanta Consultancy Services
Eingestellt
19.09.2014
Projekt-ID:
777976
Vertragsart
Freiberuflich
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