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German Speaking Quality Assurance Professional
Eingestellt von RM IT Professional Resources AG
Gesuchte Skills: Support
Projektbeschreibung
German speaking Quality Assurance Professional wanted for one of our Basel based clients in the pharmaceutical sector.
YOUR EXPERIENCE/SKILLS:
- Degree in laboratory, manufacturing or relevant discipline. B.A, B.Sc. or equivalent will be of advantage
- 2+ years of solid working experience in a corresponding line unit function (eg laboratory, manufacture, packaging, IT, documentation)
- Excellent scientific, technical and regulatory knowledge in a precise area along with knowledge of cGMPs, safety and environmental regulations and guidelines
- Strong ability to appropriately address GMP and logistic related questions with the line unit experts for maintaining GMP records in a compliant status
- Knowledge of drug development as well as ability to analyze and assess GMP compliance
- Very good organizational skills along with ability to work with relevant IT systems
- Languages: fluent German and English (both written and spoken)
YOUR TASKS:
- Providing review of GMP relevant documents for compliance with SOPs across several customer groups including manufacturing or packaging master documents and batching records for material manufactured or packaged
- Defining simple deficiencies in GMP documents with the line unit experts in own responsibility along with providing support for quality relevant electronic systems (GLIMS, TQW, TEDI, ESOP)
- Identifying complex deficiencies in GMP documents, reporting them to supervisor, proposing actions and leading agreed follow-up
- Writing GMP relevant documents in own area of responsibility beside archiving documents owned by QA
- Supporting the line function in the use of GMP relevant IT tools and processes as well as cooperating with other associates to support the service function of QA
- Taking part in knowledge exchange in TRD and in training of new and temporary employees
START: 11/2016
DURATION: 4MM++
LOCATION: Basel, Switzerland
REF.NR.: BH 9719
Does that sound interesting? Does that sound like a challenging opportunity to you? 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:
- Degree in laboratory, manufacturing or relevant discipline. B.A, B.Sc. or equivalent will be of advantage
- 2+ years of solid working experience in a corresponding line unit function (eg laboratory, manufacture, packaging, IT, documentation)
- Excellent scientific, technical and regulatory knowledge in a precise area along with knowledge of cGMPs, safety and environmental regulations and guidelines
- Strong ability to appropriately address GMP and logistic related questions with the line unit experts for maintaining GMP records in a compliant status
- Knowledge of drug development as well as ability to analyze and assess GMP compliance
- Very good organizational skills along with ability to work with relevant IT systems
- Languages: fluent German and English (both written and spoken)
YOUR TASKS:
- Providing review of GMP relevant documents for compliance with SOPs across several customer groups including manufacturing or packaging master documents and batching records for material manufactured or packaged
- Defining simple deficiencies in GMP documents with the line unit experts in own responsibility along with providing support for quality relevant electronic systems (GLIMS, TQW, TEDI, ESOP)
- Identifying complex deficiencies in GMP documents, reporting them to supervisor, proposing actions and leading agreed follow-up
- Writing GMP relevant documents in own area of responsibility beside archiving documents owned by QA
- Supporting the line function in the use of GMP relevant IT tools and processes as well as cooperating with other associates to support the service function of QA
- Taking part in knowledge exchange in TRD and in training of new and temporary employees
START: 11/2016
DURATION: 4MM++
LOCATION: Basel, Switzerland
REF.NR.: BH 9719
Does that sound interesting? Does that sound like a challenging opportunity to you? 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
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Kategorie:
Sonstiges