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Job Requirements of LIMS (Lab Information Management System) Administrator:
-
Employment Type:
Contractor
-
Location:
St. Louis, MO (Onsite)
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LIMS (Lab Information Management System) Administrator
Careers Integrated Resources Inc
St. Louis, MO (Onsite)
Contractor
Title: LIMS (Lab Information Management System) Administrator
Temp to perm potential
Experience: data management, change management, systems support, QC and QA
Required: Any LIMS software
Preferred: LabVantage software
2 people are needed
Interviews: Virtual and then on-site
Hybrid: 3 days on-site, 2 days remote
Responsible for creating, reviewing, and approving product/master data builds in LIMS per 21CFR Part 11 & EU Annex 11 guidelines and regulations including appropriate data integrity. The individual will support OC & QA operational activities by prioritizing data activities, reviewing applicable documentation and making revisions and changes as required. Additionally, this individual will act as a software administrator for LIMS software when requested, help define workflow integration of QC processes, including management of user accounts and roles. This individual will also assist in the investigation of deviations as needed, managing and executing change controls using Trackwise.
BS/BA or MS degree, life sciences preferred
3-5 years of GMP experience in pharmaceutical, biopharmaceutical or chemical industry
Prior experience with analytical testing is preferred.
Prior data entry experience recommended.
Familiarity with general laboratory instrumentation and documentation.
Working knowledge of laboratory management systems, LabVantage LIMS preferred.
Prior Instrumentation testing experience is preferred
Able to excel in a team setting in a dynamic environment where shifting priorities are not uncommon.
Strong verbal and written communication skills.
Agility to change, quick learner & critical thinking skills desired.
Temp to perm potential
Experience: data management, change management, systems support, QC and QA
Required: Any LIMS software
Preferred: LabVantage software
2 people are needed
Interviews: Virtual and then on-site
Hybrid: 3 days on-site, 2 days remote
Responsible for creating, reviewing, and approving product/master data builds in LIMS per 21CFR Part 11 & EU Annex 11 guidelines and regulations including appropriate data integrity. The individual will support OC & QA operational activities by prioritizing data activities, reviewing applicable documentation and making revisions and changes as required. Additionally, this individual will act as a software administrator for LIMS software when requested, help define workflow integration of QC processes, including management of user accounts and roles. This individual will also assist in the investigation of deviations as needed, managing and executing change controls using Trackwise.
BS/BA or MS degree, life sciences preferred
3-5 years of GMP experience in pharmaceutical, biopharmaceutical or chemical industry
Prior experience with analytical testing is preferred.
Prior data entry experience recommended.
Familiarity with general laboratory instrumentation and documentation.
Working knowledge of laboratory management systems, LabVantage LIMS preferred.
Prior Instrumentation testing experience is preferred
Able to excel in a team setting in a dynamic environment where shifting priorities are not uncommon.
Strong verbal and written communication skills.
Agility to change, quick learner & critical thinking skills desired.
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