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Quality Project Specialist
Eingestellt von RM IT Professional Resources AG
Gesuchte Skills: Support, Client
Projektbeschreibung
Quality Project Specialist wanted for our Basel based client in the pharmaceutical sector.
YOUR EXPERIENCE/SKILLS:
- Apprenticeship degree or equivalent in manufacturing, laboratory or related discipline, relevant Bachelor degree is a plus
- 2+ years' working experience in a comparable line unit function like documentation, IT, manufacture, laboratory or packaging
- Competency of cGMPs as well as safety guidelines and environmental regulations
- Basic know-how of drug development
- Languages: fluent German and adequate English, both written and spoken
YOUR TASKS:
- Maintaining GMP document management, including reviewing for SOP compliance
- Creating and completing GMP important documents in own area of responsibility, for example BRR sheets, CoCs, CoAs, SOPs and test scripts
- Identifying deficiencies and communicating them to supervisor along with suggesting actions as well as fixing simple defects
- Ensuring support for QA and process improvements, including relevant electronic systems and associates
- Acting as SME and contact person for the line unit
START: 01/2018
DURATION: 12MM+
LOCATION: Basel, Switzerland
REF.NR.: BH12073
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:
- Apprenticeship degree or equivalent in manufacturing, laboratory or related discipline, relevant Bachelor degree is a plus
- 2+ years' working experience in a comparable line unit function like documentation, IT, manufacture, laboratory or packaging
- Competency of cGMPs as well as safety guidelines and environmental regulations
- Basic know-how of drug development
- Languages: fluent German and adequate English, both written and spoken
YOUR TASKS:
- Maintaining GMP document management, including reviewing for SOP compliance
- Creating and completing GMP important documents in own area of responsibility, for example BRR sheets, CoCs, CoAs, SOPs and test scripts
- Identifying deficiencies and communicating them to supervisor along with suggesting actions as well as fixing simple defects
- Ensuring support for QA and process improvements, including relevant electronic systems and associates
- Acting as SME and contact person for the line unit
START: 01/2018
DURATION: 12MM+
LOCATION: Basel, Switzerland
REF.NR.: BH12073
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