LIMS Consultant - French
Senior Labware LIMS Consultant - 6 months contract - Remote - French Speaking
My Client is a global Pharma company and they are looking for Senior Labware LIMS Consultant who will collaborate closely with our Quality Control (QC) laboratories, leveraging their knowledge of pharmaceutical quality processes and Labware support processes to enhance and develop laboratory methods.
Key Responsibilities:
- Collaborate with laboratories to understand business requirements and translate them into technical specifications.
- Identify dependencies, risks, and issues related to development.
- Develop methods following LES standards and best practices.
- Perform Factory Acceptance Tests (FAT) as required by GQC.
- Prepare for business testing through dry-runs.
- Ensure all necessary documentation is complete before the data approval process.
Qualifications:
- Extensive knowledge of pharmaceutical quality and QC lab processes.
- Proficient in Labware HQ support processes.
- In-depth understanding of the pharmaceutical regulatory GxP environment and Electronic Laboratory Notebook (ELN).
- Familiarity with Labware design and programming standards, including visual workflows and LIMS basic.
- Fluency in both French and English is mandatory.
Preferred Skills:
- Strong analytical and problem-solving skills.
- Excellent communication and interpersonal abilities.
- Ability to work independently and as part of a team.
- Detail-oriented with a strong focus on accuracy and quality.
Reference: 2805316767
LIMS Consultant - French
Posted on Aug 7, 2024 by Red - The Global SAP Solutions Provider
Senior Labware LIMS Consultant - 6 months contract - Remote - French Speaking
My Client is a global Pharma company and they are looking for Senior Labware LIMS Consultant who will collaborate closely with our Quality Control (QC) laboratories, leveraging their knowledge of pharmaceutical quality processes and Labware support processes to enhance and develop laboratory methods.
Key Responsibilities:
- Collaborate with laboratories to understand business requirements and translate them into technical specifications.
- Identify dependencies, risks, and issues related to development.
- Develop methods following LES standards and best practices.
- Perform Factory Acceptance Tests (FAT) as required by GQC.
- Prepare for business testing through dry-runs.
- Ensure all necessary documentation is complete before the data approval process.
Qualifications:
- Extensive knowledge of pharmaceutical quality and QC lab processes.
- Proficient in Labware HQ support processes.
- In-depth understanding of the pharmaceutical regulatory GxP environment and Electronic Laboratory Notebook (ELN).
- Familiarity with Labware design and programming standards, including visual workflows and LIMS basic.
- Fluency in both French and English is mandatory.
Preferred Skills:
- Strong analytical and problem-solving skills.
- Excellent communication and interpersonal abilities.
- Ability to work independently and as part of a team.
- Detail-oriented with a strong focus on accuracy and quality.
Reference: 2805316767
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