Senior Specialist LIMS

Build your future at Curia, where our work has the power to save lives

Curia is a global contract development and manufacturing organization (CDMO) with over 30 years of experience partnering with pharmaceutical and biotech companies to provide life‑saving treatments to patients. At Curia, we are on a mission to advance our customers' therapies from curiosity to cure and ultimately to improve patients' lives.

• Generous benefit options (eligible first day of employment)
• Paid training, vacation and holidays (vacation accrual begins on first day of employment)
• Career advancement opportunities
• Education reimbursement
• 401K program with matching contributions
• Learning platform
• And more!

This role will be responsible for partnering with LIMS subject matter experts to ensure the implementation of LIMS at the Rensselaer, New York site is consistent with the program across the global network.

To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

• In collaboration with the Manager of QC Lab Remediation, lead and oversee LIMS within the quality control laboratory; support enhancements and integrations
• Lead and oversee Lab Vantage LIMS within the quality control laboratory; support enhancements and integrations.
• Validation & Compliance:
  
  Execute validation activities, ensuring compliance with GxP, data integrity, and CSV requirements.
• Documentation & SOPs:
  Maintain and update technical documentation, SOPs, and training materials.
• User Training:
  Provide support and training on LIMS including new system functionalities.
• Data Governance & Quality:
  Enforce data integrity standards, version control, and data accuracy across all laboratory processes. Ensure compliance with global corporate policies and regulatory standards (e.g., FDA 21 CFR Part 11, cGMP, ISO 17025).
• Cross‑Functional
  
  Collaboration:
  
  Partner with lab subject matter experts (SMEs) to gather business requirements and map existing workflows to system capabilities.
• Documentation:
  Own and update LIMS Standard Operating Procedures (SOPs)
• Build and maintain test definitions, sampling plans, specifications, and stability protocols in LIMS, in collaboration with QC SMEs.
• Support troubleshooting of data‑related issues.
• Work with IT System Administrator to develop user requirements and test scripts for custom scripts, code, or automation tools to support LIMS integration with analytical instruments and other enterprise systems.
• Lead QA and QC to test system settings, user roles, and permissions.
• Support internal and external regulatory audits and inspections.
• Lead QC ongoing LIMS improvements and upgrades.

• Bachelor's degree in Chemistry, Biology, Life Sciences or related field
• Minimum of 8 years of experience with pharma laboratory applications (LIMS, LES, ELN).
• Strong experience with Lab Vantage LIMS master data building
• Understanding of GxP, data integrity, and computer system validation requirements.
• Understanding of analytical testing and techniques
• Experience writing and updating technical documentation, SOPs, and training materials.

• Experience with LIMS as an end user and/or participation in an LIMS implementation.
• Software development experience with Java and/or Groovy.

• Strong analytical and problem‑solving abilities.
• Effective communication and interpersonal skills.
• Ability to work in a fast‑paced, regulated environment.
• Proactive…