LIMS/Labware Expert

Company profile

Our client is a key player in the Pharma industry worldwide. Job description

Key responsibilities

- Formalize user requirements and functional/technical specs with the business users
- Define standard solutions to support the business laboratory processes
- Drive standard good practices avoiding complex customizations
- Test of the application and write the test scripts
- Write the GxP validation documentation in coordination with IT Quality Risk & Compliance and business QA departments
- Configure, develop, maintain new and existing Labware functionalities and applications
- Work in the existing Labware template - using the current methodology and tools - and participate to extend the template

Required profile

Education and experience:

- Knowledge of pharmaceutical quality and R&D lab processes
- Knowledge of the pharmaceutical regulatory GxP environment
- Good awareness of Labware design and programming standards (visual workflows, LIMS basic,…)
- Solid knowledge of IT CSV Documentation with at least 2 years experience
- Knowledge of industry specific templates/modules

(BioAnalysis, Labware ELN,…) - Fluent in English, French is a plus
- Knowledge of Labware HQ support processes
- Good skills in project management with minimum of experience as business analyst, lab process designer and IT project leader

Personal characteristics:

- Quality first mindset
- Strong analytical capability driven by standardization and simplification
- Good communication skills
- Able to operate independently and as part of a team

Offer

Option for both frame work agreement for freelance or permanent contract.

You will be part of an international environment with the company invests in personal growth.

Interested? send us your latest version of your resume/CV to or call