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QA/QC Specialist
Eingestellt von RM IT Professional Resources AG
Gesuchte Skills: Support, Client
Projektbeschreibung
QA/QC Specialist with profound GMP knowledge wanted for our Basel based client in the pharmaceutical sector.
YOUR EXPERIENCE/SKILLS:
- Minimum: Basic degree in laboratory, manufacturing or relevant discipline (apprenticeship or equivalent)
- Desirable: Basic degree in science of relevant discipline (B.A., B.Sc. or equivalent)
- 2+ years of relevant experience in a corresponding line unit function (eg laboratory, manufacturing, packaging, IT and/or documentation)
- Extensive knowledge of cGMPs, working knowledge of safety and environmental regulations and guidelines and scientific, basic knowledge of drug development
- Excellent communication skills in order to address GMP and logistic related questions with the line unit experts to maintain GMP records in a compliant status
- Outstanding organizational skills with the ability to analyze and evaluate GMP compliance
- Sufficient knowledge of relevant IT systems
- Languages: fluent English and German, both written and spoken
YOUR TASKS:
- Performing review of GMP relevant documents for compliance with SOPs across several customer groups (eg manufacturing or packaging master documents, batch records for material manufactured and/or packaged internally or at con-tractors, TEDI documents, SOPs, analytical raw data, qualification documents etc.)
- Clarifying simple deficiencies in GMP documents with the line unit experts and recognizing complex deficiencies in GMP documents, report them to supervisor, suggest actions and supervise agreed follow-up
- Providing support for quality relevant electronic systems (eg GLIMS, TQW, TEDI, ESOP) and writing and completing GMP relevant documents in own area of responsibility
- Contributing to the evaluation of new tools (eg IT systems, processes) as well as filing and archiving documents owned by QA
- Supporting the line function in the use of GMP relevant IT tools and processes
START: ASAP
DURATION: 02MM+
LOCATION: Basel, Switzerland
REF.NR.: BH10660
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:
- Minimum: Basic degree in laboratory, manufacturing or relevant discipline (apprenticeship or equivalent)
- Desirable: Basic degree in science of relevant discipline (B.A., B.Sc. or equivalent)
- 2+ years of relevant experience in a corresponding line unit function (eg laboratory, manufacturing, packaging, IT and/or documentation)
- Extensive knowledge of cGMPs, working knowledge of safety and environmental regulations and guidelines and scientific, basic knowledge of drug development
- Excellent communication skills in order to address GMP and logistic related questions with the line unit experts to maintain GMP records in a compliant status
- Outstanding organizational skills with the ability to analyze and evaluate GMP compliance
- Sufficient knowledge of relevant IT systems
- Languages: fluent English and German, both written and spoken
YOUR TASKS:
- Performing review of GMP relevant documents for compliance with SOPs across several customer groups (eg manufacturing or packaging master documents, batch records for material manufactured and/or packaged internally or at con-tractors, TEDI documents, SOPs, analytical raw data, qualification documents etc.)
- Clarifying simple deficiencies in GMP documents with the line unit experts and recognizing complex deficiencies in GMP documents, report them to supervisor, suggest actions and supervise agreed follow-up
- Providing support for quality relevant electronic systems (eg GLIMS, TQW, TEDI, ESOP) and writing and completing GMP relevant documents in own area of responsibility
- Contributing to the evaluation of new tools (eg IT systems, processes) as well as filing and archiving documents owned by QA
- Supporting the line function in the use of GMP relevant IT tools and processes
START: ASAP
DURATION: 02MM+
LOCATION: Basel, Switzerland
REF.NR.: BH10660
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
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Kategorie:
IT Entwicklung, Sonstiges