LIMS Administrator

Description:

Our client, a global CDMO in pharmaceutical manufacturing that provides development and cGMP production in cell culture, microbial fermentation and gene therapies, is currently seeking a LIMS Administrator. This individual will be responsible for configuration, process validation, master data updates, and ongoing maintenance within the LIMS platform. They will be expected to complete and review change requests, validate configurations, provide user support, and troubleshoot as needed. Prior experience within a QC lab will be helpful in understanding the links between benchwork and updating processes within their LIMS.

Skills:

LabWare LIMS

LIMS

cGMP

Change controls

QC laboratory

LIMS configuration

Troubleshooting

Master data updates

Minimum Qualifications:

Bachelors degree, ideally within a scientific major

Minimum of 3-4 years experience with LabWare LIMS (development and/or working within) in a cGMP QC biologics facility [*some LIMS experience from other industries allowed - i.e. food, engineering, cosmetics, chemical]

Experience with LIMS configuration

Ability to work a first shift, hyrbid schedule

Experience Level:

Intermediate Level