Dieses Jobangebot ist archiviert und steht nicht mehr zur Verfügung.
Vakante Jobangebote finden Sie unter Projekte.
Vakante Jobangebote finden Sie unter Projekte.
QA Validation Specialist
Eingestellt von Quanta Consultancy Services
Gesuchte Skills: Engineering, Support
Projektbeschreibung
A world leading bio-pharmaceutical organisation is looking for a QA Validation Specialist to work on a major investment project in South East Asia. The project is a $300m+ biologics site.
The QA Validation Specialist will focus on the newly installed laboratory equipment in support of the main manufacturing. The first six months will be spent in the company's global headquarters, after which activities will be spent on site.
Location: Switzerland (until Dec 2013), South East Asia (from Jan 2014 onwards)
Duration: 18 months +
Role and Responsibilities:
Reviewing DQ and equipment procurement documentation for technical integrity and GMP compliance
Planning qualification and validation activities from the global headquarters (Switzerland)
Executing IQ/OQ/PQ protocols and process validation tests on site (on site - South East Asia)
Providing QA oversight to all activities to ensure that the new site will be fully compliant
Working with lab equipment such as HPLC, GC, UV, UF
Requirements:
Engineering background with experience working on biopharmaceutical investment projects
Experience planning, executing and reviewing qualification and validation of equipment and processes
Experience working with lab and analytical equipment
Strong GMP knowledge
Confident working in international, multicultural environments
This is an excellent opportunity to work on one of the biggest start-up biotech sites in the world for a top blue chip company.
The QA Validation Specialist will focus on the newly installed laboratory equipment in support of the main manufacturing. The first six months will be spent in the company's global headquarters, after which activities will be spent on site.
Location: Switzerland (until Dec 2013), South East Asia (from Jan 2014 onwards)
Duration: 18 months +
Role and Responsibilities:
Reviewing DQ and equipment procurement documentation for technical integrity and GMP compliance
Planning qualification and validation activities from the global headquarters (Switzerland)
Executing IQ/OQ/PQ protocols and process validation tests on site (on site - South East Asia)
Providing QA oversight to all activities to ensure that the new site will be fully compliant
Working with lab equipment such as HPLC, GC, UV, UF
Requirements:
Engineering background with experience working on biopharmaceutical investment projects
Experience planning, executing and reviewing qualification and validation of equipment and processes
Experience working with lab and analytical equipment
Strong GMP knowledge
Confident working in international, multicultural environments
This is an excellent opportunity to work on one of the biggest start-up biotech sites in the world for a top blue chip company.
Projektdetails
Geforderte Qualifikationen
-
Kategorie:
Ingenieurwesen/Technik, Sonstiges