Dieses Jobangebot ist archiviert und steht nicht mehr zur Verfügung.
Vakante Jobangebote finden Sie unter Projekte.
Vakante Jobangebote finden Sie unter Projekte.
Validation Engineer
Eingestellt von RM IT Professional Resources AG
Gesuchte Skills: Engineer, Engineering, Client, Network
Projektbeschreibung
Contract - Validation Engineer wanted for our client based in Zurich
YOUR EXPERIENCE/SKILLS:
- PhD/MS along with 7+ years/BS along with 10+ years of experience in cGMP validation for commercial bulk and sterile process operations in vaccines or biopharmaceuticals
- Solid working experience with drug substance manufacturing, product formulation, aseptic filling, CIP/SIP and isolator technology
- Working experience in Lyophilization, vision inspection systems extractable/leachable assessments, packaging qualification and shipping validation
- Excellent knowledge of qualifying drug substance and aseptic drug product manufacturing operations to meet global regulatory requirements
- Strong ability in working with efficiency across multiple project teams and business functions in a Matrix environment plus ability to lead and manage technical teams, serve as a partner and influence others
- Languages: fluent English and German both written and spoken
YOUR TASKS:
- Establishing and starting state-of-the-art validation solutions for production of vaccine products in the Vaccine Business Unit (VBU) portfolio
- Introducing global standards for the validation of equipment, facilities, and processes to drive consistency across operations within the Global VBU Manufacturing Network beside providing support for CAPA management and deviation investigations
- Providing validation technical leadership for the design, construction, start-up and qualification of new vaccine manufacturing facilities/processes
- Employing external networks to identify resources and build partnerships in the areas of validation technologies to drive best in class manufacturing operations
- Working together with development teams, site operations and engineering teams to generate and execute process/product technology transfers and the associated qualification/validation activities for strategic growth initiatives
- Supporting the development of planning and execution for validation activities with the transfer of products from development into commercial manufacturing and commercial site transfers
START: 10/2016
DURATION: 6MM++
LOCATION: Zurich, Switzerland
REF.NR.: BH9565
Does that sound interesting? Then take the next step and send us your CV as a Word Document and a daytime contact telephone number.
DUE TO WORK PERMIT RESTRICTIONS WE CAN UNFORTUNATELY ONLY CONSIDER APPLICATIONS FROM EU OR SWISS CITIZENS AS WELL AS CURRENT WORK-PERMIT HOLDERS FOR SWITZERLAND.
GOING THE EXTRA MILE
NEW TO SWITZERLAND? In case of successful placement, we support you with:
- All administrative questions
- Finding an apartment
- Health - and social insurance
- Work permit and much more
YOUR EXPERIENCE/SKILLS:
- PhD/MS along with 7+ years/BS along with 10+ years of experience in cGMP validation for commercial bulk and sterile process operations in vaccines or biopharmaceuticals
- Solid working experience with drug substance manufacturing, product formulation, aseptic filling, CIP/SIP and isolator technology
- Working experience in Lyophilization, vision inspection systems extractable/leachable assessments, packaging qualification and shipping validation
- Excellent knowledge of qualifying drug substance and aseptic drug product manufacturing operations to meet global regulatory requirements
- Strong ability in working with efficiency across multiple project teams and business functions in a Matrix environment plus ability to lead and manage technical teams, serve as a partner and influence others
- Languages: fluent English and German both written and spoken
YOUR TASKS:
- Establishing and starting state-of-the-art validation solutions for production of vaccine products in the Vaccine Business Unit (VBU) portfolio
- Introducing global standards for the validation of equipment, facilities, and processes to drive consistency across operations within the Global VBU Manufacturing Network beside providing support for CAPA management and deviation investigations
- Providing validation technical leadership for the design, construction, start-up and qualification of new vaccine manufacturing facilities/processes
- Employing external networks to identify resources and build partnerships in the areas of validation technologies to drive best in class manufacturing operations
- Working together with development teams, site operations and engineering teams to generate and execute process/product technology transfers and the associated qualification/validation activities for strategic growth initiatives
- Supporting the development of planning and execution for validation activities with the transfer of products from development into commercial manufacturing and commercial site transfers
START: 10/2016
DURATION: 6MM++
LOCATION: Zurich, Switzerland
REF.NR.: BH9565
Does that sound interesting? Then take the next step and send us your CV as a Word Document and a daytime contact telephone number.
DUE TO WORK PERMIT RESTRICTIONS WE CAN UNFORTUNATELY ONLY CONSIDER APPLICATIONS FROM EU OR SWISS CITIZENS AS WELL AS CURRENT WORK-PERMIT HOLDERS FOR SWITZERLAND.
GOING THE EXTRA MILE
NEW TO SWITZERLAND? In case of successful placement, we support you with:
- All administrative questions
- Finding an apartment
- Health - and social insurance
- Work permit and much more
Projektdetails
Geforderte Qualifikationen
-
Kategorie:
IT Entwicklung, Ingenieurwesen/Technik