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Process Manager (Sterile Production)
Eingestellt von RM IT Professional Resources AG
Gesuchte Skills: Client, Support
Projektbeschreibung
Process Manager with extensive knowledge in Sterile Production wanted for our Basel based client in the pharmaceutical sector.
YOUR EXPERIENCE/SKILLS:
- BSc. in Pharmacy, Pharmaceutical Technology or Chemistry, preferably with Project management experience and technical understanding of Sterile Production Processes
- 5+ years of relevant experience in pharmaceutical manufacturing
- Outstanding project management skills and team lead experience is mandatory
- Comprehensive knowledge in pharmaceutical technology and deep knowledge in cGMP, HSE and Regulatory
- Languages: fluent English both written and spoken, German would be an asset
YOUR TASKS:
- Managing technical activities on site level for product tranfers as well as providing technical expertise and defining and monitoring project scope, timing and progress
- Writing Manufacturing Process Transfer Documents (protocol, reports) and coordinating feasibility, regulatory and validation batches at site
- Supporting continuous process and quality improvements, likewise ensuring inspection (PAI: Pre-Approval Inspection) readiness
- Commencing and monitoring and CPV (continued process validation) phase
START: ASAP
DURATION: 11MM+
LOCATION: Basel, Switzerland
REF.NR.: BH12289
Does this sound like an interesting and challenging opportunity to you? Then take the next step by sending us your CV as a Word document and a 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:
- BSc. in Pharmacy, Pharmaceutical Technology or Chemistry, preferably with Project management experience and technical understanding of Sterile Production Processes
- 5+ years of relevant experience in pharmaceutical manufacturing
- Outstanding project management skills and team lead experience is mandatory
- Comprehensive knowledge in pharmaceutical technology and deep knowledge in cGMP, HSE and Regulatory
- Languages: fluent English both written and spoken, German would be an asset
YOUR TASKS:
- Managing technical activities on site level for product tranfers as well as providing technical expertise and defining and monitoring project scope, timing and progress
- Writing Manufacturing Process Transfer Documents (protocol, reports) and coordinating feasibility, regulatory and validation batches at site
- Supporting continuous process and quality improvements, likewise ensuring inspection (PAI: Pre-Approval Inspection) readiness
- Commencing and monitoring and CPV (continued process validation) phase
START: ASAP
DURATION: 11MM+
LOCATION: Basel, Switzerland
REF.NR.: BH12289
Does this sound like an interesting and challenging opportunity to you? Then take the next step by sending us your CV as a Word document and a 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, Sonstiges