LIMS Administrator, Pennsylvania

Job Description:

As a Lab Information Management System [LIMS] Business Administrator, you are responsible to support the maintenance and improvement of the LIMS system to Quality Operations. Maintenance support will include supporting Business Administrators in, updating master data for new and existing products, updating master data for new and existing analysis, maintaining system documentation, and providing ad hoc support to other departments. The position is expected to provide leadership to support system evolution and continuous improvement, and to support laboratory informatics needs. This role will support the creation and updating of master data to support the site transition to toa new ERP. Translation of data from existing documents to the electronic system for use in production and QC.

 

Position Responsibilities:

Ensure site on-time implementation of new iSHIFT system (ERP) activities through support of master data configuration and data migration and SOP revisions.

Provide technical support of LIMS to Quality Control, Batch Release, Production, Stability and R&D operations

Provide first level diagnostic of incidents and support business users, IS LIMS Administrator and Support Center in the management and timely resolution of technical

Responsible for the master data management process including the updating of specifications and supporting the approval process

Manage Global System update and changes which may include new modules and workflow changes

Configure and Maintain instrument interfaces to Laboratory equipment

Ensure that the LIMS complies with all relevant regulatory standards

Support the business in the creation and updating of training materials as changes to system occur

Ensure that the LIMS complies with all relevant regulatory standards

 

Experience & Skills:

Must have 1+ years of experience in use and administration of LabWare LIMS specifically creation of product specs, sample plans and item codes.

Strong working knowledge of laboratory processes including cGMP’s in a pharmaceutical environment

Experience in system testing, validation, and master data management

Working knowledge of aseptic processes, biology, chemistry, life sciences

Knowledge of cGMPs and regulatory requirements with Strong analytical & balanced decision-making skills. Good GMP documentation

Familiar with 21CFR part 11 data integrity best practices in pharmaceutical environment

Excellent written and verbal communications skills and the ability to lead and participate in teams

Experience or familiarity of the Laboratory Environment

 

 

The hourly range for roles of this nature are $50.00 to $80.00/hr. Rates are heavily dependent on skills, experience, location, and industry.

 

cyberThink is an Equal Opportunity Employer.