Find & Apply For Data Warehousing Specialist Jobs in Swiftwater, Pennsylvania

LIMS Data Specialist Pay Rate:

$58.00-$76.00/hour

Schedule:

1st Shift, 8:00 AM-4:30

PM EST Location:

Swiftwater, PA - Onsite Sanofi's contingent workforce program, FLEXT Direct, is seeking a LIMS Data Specialist for a 3-month contract supporting Quality Operations at the Swiftwater site. Position Overview The Lab Information Management System (LIMS) Business Administrator is essential to Quality Operations at the Swiftwater site, supporting the maintenance and improvement of the LIMS system. Responsibilities include supporting the business by updating master data for new and existing products and analyses, maintaining system documentation, and providing ad hoc support to other departments. The role will also support the creation and updating of master data, including Product Specifications, Item Codes, and Sampling Plans, in support of data remediation and SPC projects. Position Responsibilities Ensure on-time implementation of data remediation activities through support of master data configuration, data migration, and SOP revisions. Support the master data management process, including updating specifications and analyses and supporting the approval and verification process. Ensure that the LIMS complies with relevant regulatory standards. Support the business in creating and updating training materials as system changes occur. Technical Competencies & Soft Skills Working knowledge of aseptic processes, biology, chemistry, or life sciences. Knowledge of cGMPs and applicable regulatory requirements. Strong analytical and balanced decision-making skills. Excellent written and verbal communication skills. Ability to lead and participate effectively in teams. Experience working in a laboratory environment. Basic Requirements 1-3 years of experience using and administering LabWare LIMS, including LIMS Basic. Strong working knowledge of laboratory processes, including cGMPs, in a pharmaceutical environment. Experience with system validation and master data management. Familiarity with 21 CFR Part 11 data-integrity best practices in a pharmaceutical environment. Excellent written and verbal communication skills and the ability to lead and participate in teams. Experience or familiarity with the laboratory environment.