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QA/QC Specialist
Eingestellt von RM IT Professional Resources AG
Gesuchte Skills: Client, Support
Projektbeschreibung
QA/QC Specialist with profound GMP knowledge wanted for our Basel based client in the pharmaceutical sector.
YOUR EXPERIENCE/SKILLS:
- Degree in scientific, laboratory, manufacturing or relevant discipline
- Several 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
- Clarifying simple deficiencies in GMP documents with the line unit experts
- Reporting complex deficiencies in GMP documents to supervisor, suggesting actions and supervising agreed follow-up
- Acting as contact person for QA questions of quality relevant electronic systems (eg IMOS, GLIMS, TQW, QP database, TEDI, ESOPS, Pathlore) and/or as a contact person to the needs of the line unit
- Writing and completing GMP relevant documents in own area of responsibility (eg CoAs, CoCs, BRR sheets, test scripts, SOPs with extended applicability)
- Supporting the line function in the use of GMP relevant IT tools and processes
- Participating in training and on-boarding of new team members
START: ASAP
DURATION: 3MM+
Location: Basel, Switzerland
Ref.Nr.: BH11366
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:
- Degree in scientific, laboratory, manufacturing or relevant discipline
- Several 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
- Clarifying simple deficiencies in GMP documents with the line unit experts
- Reporting complex deficiencies in GMP documents to supervisor, suggesting actions and supervising agreed follow-up
- Acting as contact person for QA questions of quality relevant electronic systems (eg IMOS, GLIMS, TQW, QP database, TEDI, ESOPS, Pathlore) and/or as a contact person to the needs of the line unit
- Writing and completing GMP relevant documents in own area of responsibility (eg CoAs, CoCs, BRR sheets, test scripts, SOPs with extended applicability)
- Supporting the line function in the use of GMP relevant IT tools and processes
- Participating in training and on-boarding of new team members
START: ASAP
DURATION: 3MM+
Location: Basel, Switzerland
Ref.Nr.: BH11366
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