Catalent

Pharmaceutical

LIMSSystemAdministrator

$0–0k Greenville, North Carolina, United States FULL TIME
Market Sentiment
HIGH DEMAND

Neural analysis suggests this role is
optimal for Mid+ candidates.

The Brief

“LIMS System Administrator at Catalent. Skills: LIMS System Administration, Laboratory Compliance, System Implementation. Perform system user access management. Manage domain user groups”

Industry & Context.

Pharmaceutical
Problems you'll solve

Resolve end-user issues

Eligibility Requirements

Ability to work in a manufacturing environment, Ability to stand for extended periods, Ability to walk for extended periods, Ability to sit for extended periods, Lift up to 25 lbs

What They're Looking For.

Must Have

Bachelor's degree in Computer Science, Life Sciences, Engineering, or STEM-related field with at least 5 years of experience in the pharmaceutical industry or relevant laboratory experience in a related industry, Associate's degree in Computer Science, Life Sciences, Engineering, or STEM-related field with at least 7 years of experience in the pharmaceutical industry or relevant laboratory experience in a related industry, Experience with LIMS or a Material Management System, Knowledge of cGMP and other regulatory requirements relative to LIMS systems, Software validation experience

Nice to Have

LabVantage experience preferred, Hands-on experience with GROOVY or Java scripting to configure and optimize ELN/LES method workflows, including calculation logic and automated data handling preferred

What You'll Do.

Perform system user access management

Manage domain user groups

Conduct routine access reviews

Manage Windows folder access

Synchronize date/time

Resolve end-user LIMS template issues

Resolve end-user LIMS data entry issues

Identify operational improvement opportunities

Lead cross-functional teams

Develop site-specific User Requirements

Ensure LIMS compliance with GxP

Define project deliverables

Develop LIMS-specific SOPs

Manage software updates

Manage software patches

Perform routine maintenance

Author validation documentation

Support validation documentation

Author system procedures

Support system procedures

Support training for end users

Hand off LIMS during new hire orientation

Perform other duties as assigned

How You'll Work.

Team & Collaboration

Cross-functional teams; Laboratory personnel; Operations personnel; EH&S personnel; Quality personnel; IT personnel; CSV personnel; Global system owners

Process & Methodology

Project scope definition, Goal setting, Deliverable definition

Full Job Description

**LIMS System Administrator** **Position Summary** * The shift is Monday - Friday from 8 am - 4:30 pm. * ​This position is 100% on-site at the Greenville site. The LIMS System Administrator will implement LabVantage Laboratory Information Management System (LIMS) at the Catalent Greenville site. This position is responsible for developing, managing, and implementing the laboratory administration and compliance program for LIMS to ensure compliance with local and global regulatory agency requirements, internal company standards, and current industry practices. Additionally, the LIMS System Administrator will lead cross-functional teams comprised of laboratory, operations, EH&S, and Quality personnel at the Greenville facility and other Catalent sites to expand and improve the use of the LIMS system and to design and implement added-value applications within the LIMS environment. Catalent’s Greenville, N.C. facility specializes in end-to-end turn-key solutions for oral solid dosage forms, including integrated formulation development, analytical services, commercial manufacturing, and packaging. This state-of-the-art facility has had over $100M of investments in recent years and features fit-for-scale capacity with potent handling capabilities, ideal for orphan or targeted drug development. **The Role:** * Perform and support system user access management, including domain user groups, routine access reviews, Windows folder access, and date/time synchronization, as well as resolving end‑user LIMS template and data entry issues. * Identify operational improvement opportunities which LIMS can provide solutions * Lead cross‑functional teams to develop site‑specific User Requirements in a harmonized format, and collaborate with IT, Quality, CSV, and global system owners to ensure LIMS complies with all applicable GxP, legal, and fiduciary policies and requirements. * Define project scope, goals and deliverables that support business goals in collaboration with senior manag

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