The main focus of the C#/.Net Developer will be new features development for the client’s plateform. This includes specifications, development, tests activities and documentation reviews.
Software Engineering, Computer Science Engineering or Telecommunication Engineering degree.
Required software development best practices (C++ and C#/ Net, Visual Studio, Angular).
Participation in the testing activities: unit tests, integration tests, test automation with Selenium.
Rigorous mindset, attention to details.
Fluent in English; French and Italian an asset.
Good understanding and proven experience working under software project methodologies (Waterfall, Agile).
Experience in regulated environment or Hospital IT is a plus.
Strong interpersonal skills, excellent oral and written communication.
Team player on internal/external, national/international teams.
Autonomous, must be able to work with minimal supervision.
janv. 09, 2021
Contrat CDI
The main focus of the C#/.Net Developer will be new features development for the client’s plateform. This includes specifications, development, tests activities and documentation reviews.
Software Engineering, Computer Science Engineering or Telecommunication Engineering degree.
Required software development best practices (C++ and C#/ Net, Visual Studio, Angular).
Participation in the testing activities: unit tests, integration tests, test automation with Selenium.
Rigorous mindset, attention to details.
Fluent in English; French and Italian an asset.
Good understanding and proven experience working under software project methodologies (Waterfall, Agile).
Experience in regulated environment or Hospital IT is a plus.
Strong interpersonal skills, excellent oral and written communication.
Team player on internal/external, national/international teams.
Autonomous, must be able to work with minimal supervision.
Define the technology transfer strategy
Support the technology transfers and process validation to the new biotech production site
Support the implementations and performance of Quality operations (new process introduction, electronic batch records, change controls, quality events, periodic reviews, change-over management and others)
Act within compliance and legal requirements as well as within company guidelines
Work with the project team and the engineering companies on the detailed design deliverables concerning process equipment requirements and actively support the risk assessment exercises (FMECA)
Review and approve process equipment related documentation (procedures, layouts, FAT/SAT protocols and reports, qualification protocols and reports, CAPAs, deviations and change controls) to ensure compliance with cGMP and applicable regulations
Support the Commissioning & Qualification activities during FAT at supplier’s and on site in close collaboration with manufacturing...
oct. 06, 2020
Contrat CDI
Define the technology transfer strategy
Support the technology transfers and process validation to the new biotech production site
Support the implementations and performance of Quality operations (new process introduction, electronic batch records, change controls, quality events, periodic reviews, change-over management and others)
Act within compliance and legal requirements as well as within company guidelines
Work with the project team and the engineering companies on the detailed design deliverables concerning process equipment requirements and actively support the risk assessment exercises (FMECA)
Review and approve process equipment related documentation (procedures, layouts, FAT/SAT protocols and reports, qualification protocols and reports, CAPAs, deviations and change controls) to ensure compliance with cGMP and applicable regulations
Support the Commissioning & Qualification activities during FAT at supplier’s and on site in close collaboration with manufacturing...
As a consultant, you will support the qualification and validation commissioning and qualification of labs equipments
Key responsibilities :
Act as the main point of contact for all quality compliance key topics regarding labs equipments
Review and approve the URS and relevant documentation and support actively the risk assessment exercises (FMECA)
Support the Commissioning & Qualification activities
Support the creation of procedures, protocols and reports for qualification / validation
Ensure qualification and validation of labs equipments
Act within compliance and legal requirements as well as within company guidelines
Foster the understanding and the application of Good Manufacturing Practices (cGMPs) by bioplant employees
Implementation and ensures adherence of appropriate regulations and quality standards,
Write, review and approve Standard Operating Procedures (SOPs), Quality Risk Assessments (QRAs), specifications, Batch Production Documents (BPDs) or Manufacturing...
oct. 06, 2020
Contrat CDI
As a consultant, you will support the qualification and validation commissioning and qualification of labs equipments
Key responsibilities :
Act as the main point of contact for all quality compliance key topics regarding labs equipments
Review and approve the URS and relevant documentation and support actively the risk assessment exercises (FMECA)
Support the Commissioning & Qualification activities
Support the creation of procedures, protocols and reports for qualification / validation
Ensure qualification and validation of labs equipments
Act within compliance and legal requirements as well as within company guidelines
Foster the understanding and the application of Good Manufacturing Practices (cGMPs) by bioplant employees
Implementation and ensures adherence of appropriate regulations and quality standards,
Write, review and approve Standard Operating Procedures (SOPs), Quality Risk Assessments (QRAs), specifications, Batch Production Documents (BPDs) or Manufacturing...
