Income Auditor
Income Auditor
Posted on :
08-04-2024
Employer Active
1 Vacancy
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Job Description
Req ID : 2397756
EURHASI recruits for its client a CSV Engineer
Our client is a Swiss company composed of a passionate team of experienced Life Sciences
Since 2014 we deliver outstanding industry s expertise and support to our clients in the complete product life cycle such as: R&D, Engineering and Construction, Quality management (Quality Assurance, Qualification/Validation, QC, ), Regulatory Affairs, Manufacturing, Maintenance, Operational Excellence, and Project
La mission
- You provide support and expertise on Computer System Validation activities
- You run CSV projects execution ensuring timelines are met
- You write validation plan, URS, FS, risk assessment, IQ/OQ/PQ protocols, reports, VSR, applicable SOPs and training documents
- You train and coach people
- You maintain expertise in current and emerging cGMP requirements and quality trends
- You work independently and successfully solve problems and complete/qualify a system within given constraint of scope, time and schedule
- You lead system qualification efforts and are the primary client contact for coordinating work, reporting status, resolving issues, and addressing change orders as they apply
- You develop new and pragmatic approaches to support the industry in this field
Profil
Profile
You possess at least 3 years of experience in the field of computer system validation that you developed in Pharmaceuticals, Biotechnologies or Medical devices industries
You have experience with all pertinent industry best practices (GAMP 5, ) including development and execution of all applicable system life cycle deliverables (, URS, SRS, FRS, DDS, RTM, Unit, Integration, User Acceptance testing, FAT, SAT, Validation Planning, IQ, OQ, PQ, Final Validation Summary Report)
You have previous automation experience and experiences with MES, ERP and LIMS
You possess experience in project execution within at least one area of systems validation , laboratory equipment, facilities, utilities, manufacturing equipment,
metrology equipment, information systems
You are willing to work in Switzerland
- Master s degree in a scientific or engineering discipline
- Fluent in French with good knowledge of English
Informations contractuelles
Benefits
- Telework
- Very competitive compensation package with exceptional Pension scheme
- 5 weeks paid holidays
- Ongoing Training & Development opportunities
You possess at least 3 years of experience in the field of computer system validation that you developed in Pharmaceuticals, Biotechnologies or Medical devices industries You have experience with all pertinent industry best practices (GAMP 5, ) including development and execution of all applicable system life cycle deliverables (, URS, SRS, FRS, DDS, RTM, Unit, Integration, User Acceptance testing, FAT, SAT, Validation Planning, IQ, OQ, PQ, Final Validation Summary Report) You have previous automation experience and experiences with MES, ERP and LIMS You possess experience in project execution within at least one area of systems validation , laboratory equipment, facilities, utilities, manufacturing equipment,metrology equipment, information systems You are willing to work in Switzerland Master s degree in a scientific or engineering discipline Fluent in French with good knowledge of English
Employment Type
Full Time
Department / Functional Area
Key Skills
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