About Our Client Prestigious pharmaceutical company
Contract Details Temporary contract until the end of the year. Start: first week of September.
Job Description
Act as the Single Point of Contact (SPOC) for Quality regarding deviations, returns, temperature excursions, incidents, and CAPAs.
Initiate, manage, and maintain deviation records within the Veeva Quality Management System (QMS), ensuring timely investigation, documentation, and closure.
Coordinate and follow up on investigations with internal stakeholders and third‑party logistics providers (3PLs) as required.
Plan, facilitate, and lead Root Cause Analysis (RCA) activities involving cross‑functional teams and external partners.
Collaborate with cross‑functional teams to define, implement, and monitor Corrective and Preventive Actions (CAPAs) to ensure effective deviation resolution.
Work closely with Operations, Quality Assurance (QA), the O2I Team, and external logistics partners to support timely incident and deviation management.
Support the investigation and resolution of customer‑related quality issues with a high level of accuracy and compliance.
Maintain accurate records of deviations and temperature excursions in SharePoint.
Monitor incident management activities in close collaboration with the O2I Team.
Participate in regular governance meetings, including: Weekly Distribution/QA meetings
Bi‑monthly Operations Review meetings with 3PL partners
Monthly Business Review meetings with external logistics providers
The Successful Applicant Education & Experience
Bachelor's degree or equivalent qualification in Pharmacy, Life Sciences, Chemistry, Supply Chain, or a related discipline.
Minimum of 5-7 years of experience in the pharmaceutical industry, preferably in GDP, Quality Assurance, Quality Management, or Supply Chain.
Solid understanding of Good Distribution Practice (GDP), deviation management, CAPA processes, and Root Cause Analysis methodologies.
Technical Skills
Advanced knowledge of Veeva QMS.
Good working knowledge of SAP.
Proficient in Microsoft Office applications (Word, Excel, PowerPoint).
Experience working with SharePoint.
What's on Offer Interested to support this project, during a peek phase? Looking forward to your application.
#J-18808-Ljbffr
Contract Details Temporary contract until the end of the year. Start: first week of September.
Job Description
Act as the Single Point of Contact (SPOC) for Quality regarding deviations, returns, temperature excursions, incidents, and CAPAs.
Initiate, manage, and maintain deviation records within the Veeva Quality Management System (QMS), ensuring timely investigation, documentation, and closure.
Coordinate and follow up on investigations with internal stakeholders and third‑party logistics providers (3PLs) as required.
Plan, facilitate, and lead Root Cause Analysis (RCA) activities involving cross‑functional teams and external partners.
Collaborate with cross‑functional teams to define, implement, and monitor Corrective and Preventive Actions (CAPAs) to ensure effective deviation resolution.
Work closely with Operations, Quality Assurance (QA), the O2I Team, and external logistics partners to support timely incident and deviation management.
Support the investigation and resolution of customer‑related quality issues with a high level of accuracy and compliance.
Maintain accurate records of deviations and temperature excursions in SharePoint.
Monitor incident management activities in close collaboration with the O2I Team.
Participate in regular governance meetings, including: Weekly Distribution/QA meetings
Bi‑monthly Operations Review meetings with 3PL partners
Monthly Business Review meetings with external logistics providers
The Successful Applicant Education & Experience
Bachelor's degree or equivalent qualification in Pharmacy, Life Sciences, Chemistry, Supply Chain, or a related discipline.
Minimum of 5-7 years of experience in the pharmaceutical industry, preferably in GDP, Quality Assurance, Quality Management, or Supply Chain.
Solid understanding of Good Distribution Practice (GDP), deviation management, CAPA processes, and Root Cause Analysis methodologies.
Technical Skills
Advanced knowledge of Veeva QMS.
Good working knowledge of SAP.
Proficient in Microsoft Office applications (Word, Excel, PowerPoint).
Experience working with SharePoint.
What's on Offer Interested to support this project, during a peek phase? Looking forward to your application.
#J-18808-Ljbffr
GDP Quality Coordinator Arbeitgeber: Michael Page International (Switzerland) SA
Unser Kunde ist ein bedeutender Akteur im öffentlichen Sektor in Genf und bietet eine dynamische Arbeitsumgebung, die Vielfalt und strategische Herausforderungen in den Bereichen Personalwesen fördert. Die Unternehmenskultur legt großen Wert auf Zusammenarbeit und persönliche Entwicklung, wodurch Mitarbeiter die Möglichkeit haben, ihre Fähigkeiten in einem unterstützenden Umfeld zu erweitern. Zudem profitieren Sie von einer hohen Sichtbarkeit in Ihrer Rolle, was Ihnen erlaubt, aktiv zur Weiterentwicklung der HR-Praktiken beizutragen.
Kontaktdaten:
Michael Page International (Switzerland) SA Recruiting-Team
