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Computerized System Validation (CSV) Expert
Eingestellt von RM IT Professional Resources AG
Gesuchte Skills: Engineering, Client
Projektbeschreibung
Computerized System Validation (CSV) Expert wanted for our Basel based client in the pharmaceutical sector.
YOUR EXPERIENCE/SKILLS:
- Master's Degree in Engineering, IT, Science or other computer related disciplines
- At least 5 years' experience in Computer System Validation in the pharmaceutical area with excellent project management skills
- Familiarity with GxP system as well as the ability to prioritize assignments
- Outstanding analytical and problem solving skills with willingness to work in an international environment
- Languages: fluent English both written and spoken, knowledge in German is a plus
YOUR TASKS:
- Running QA reviews and approvals of IT SOPs, user and functional requirements for new and existing computer systems, and all validation related documentation (eg User Requirements)
- Building and ensuring good and close working relationship with important project stakeholders and internal customers
- Reviewing and approving deliverables related to CSV in a GMP laboratory environment
- Collaborating with all system owners to ensure company systems continue to conform to MHRA & FDA requirements for Data Integrity within computer based systems
START: ASAP
DURATION: 5MM+
LOCATION: Basel, Switzerland
REF.NR.: BH11302
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:
- Master's Degree in Engineering, IT, Science or other computer related disciplines
- At least 5 years' experience in Computer System Validation in the pharmaceutical area with excellent project management skills
- Familiarity with GxP system as well as the ability to prioritize assignments
- Outstanding analytical and problem solving skills with willingness to work in an international environment
- Languages: fluent English both written and spoken, knowledge in German is a plus
YOUR TASKS:
- Running QA reviews and approvals of IT SOPs, user and functional requirements for new and existing computer systems, and all validation related documentation (eg User Requirements)
- Building and ensuring good and close working relationship with important project stakeholders and internal customers
- Reviewing and approving deliverables related to CSV in a GMP laboratory environment
- Collaborating with all system owners to ensure company systems continue to conform to MHRA & FDA requirements for Data Integrity within computer based systems
START: ASAP
DURATION: 5MM+
LOCATION: Basel, Switzerland
REF.NR.: BH11302
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, Ingenieurwesen/Technik