CSV Support Engineer

Overview

On Site
Full Time

Skills

Project Management
Reporting
Customization
Data Link Layer
Network Layer
Quality Control
UV
Data Acquisition
URS
DirectShow
DS
IQ
OQ
PQ
Test Scripts
Traceability Matrix
Auditing
Backup
Disaster Recovery
Quality Assurance
Change Control
Technology Assessment
HPLC
Mentorship
Process Improvement
Data Integrity
Soft Skills
Agile
Scrum
JIRA
Microsoft Azure
DevOps
Chromatography
Management
Regulatory Compliance
GxP
Computerized System Validation
Continuous Improvement
Informatics
Recruiting
Training
Analytical Skill
Conflict Resolution
Problem Solving
Documentation
Communication
Collaboration
LIMS
ELN
Pharmaceutics
Medical Devices
Computer Networking
SQL
Oracle
Database
IT Infrastructure

Job Details

Responsibilities:
  • Empower Administration & Support.
  • Manage user accounts, access rights, roles, and privileges in Empower.
  • Perform system configuration, project management, and template/report customization.
  • Provide day-to-day L2/L3 support for Empower users across QC/analytical labs.
  • Instrument Integration & Troubleshooting.
  • Integrate lab instruments (HPLC, UPLC, Dissolution, UV, etc.) with Empower.
  • Troubleshoot connectivity, data acquisition, and communication issues between instruments and CDS.
  • Work with vendors (e.g., Waters, Agilent, Thermo) for resolution of technical issues.
  • Support Computer System Validation (CSV) activities for Empower and integrated lab systems.
  • Develop and maintain validation documentation (URS, FS, DS, IQ, OQ, PQ, Test Scripts, Traceability Matrix).
  • Ensure compliance with GxP, 21 CFR Part 11, Annex 11, and internal SOPs.
  • Participate in audits and inspections, providing system and compliance evidence.
  • Maintain audit trails, backup, archival, and disaster recovery procedures.
  • Conduct periodic system reviews and ensure alignment with regulatory requirements.
  • Collaborate with QA, IT, and Lab teams to manage change control and deviations.
Requirements:
  • ny bachelor's degree Experience Range 8-12 years.
  • Primary (Must have skills) * - To be Screened by TA Team 3+ years of hands-on experience in Empower CDS administration and support.
  • 3+ years of experience on HPLC/UPLC and other analytical instrument integration.
  • 3+ years of experience on Computer System Validation (CSV) and preparation of validation deliverables.
  • 1+ year on GxP, 21 CFR Part 11, Annex 11, ALCOA+ principles, and Data Integrity requirements.
Training & Continuous Improvement:
  • Train and mentor lab users on Empower functionalities and best practices.
  • Propose process improvements for data integrity, system efficiency, and compliance.
  • Soft skills/other skills - To be Evaluated by Hiring Manager (To define how this will be evaluated) Communication Skills:
  • Communicate effectively with internal and customer stakeholders.
  • Communication approach: verbal, emails and instant messages.
Interpersonal Skills:
  • Strong interpersonal skills to build and maintain productive relationships with team members.
  • Provide constructive feedback during code reviews and be open to receiving feedback on your own code.
  • Problem-Solving and Analytical Thinking:
  • Capability to troubleshoot and resolve issues efficiently.
  • nalytical mindset.
  • Task/ Work Updates.
  • Prior experience in working on Agile/Scrum projects with exposure to tools like Jira/Azure DevOps.
  • Provides regular updates, proactive and due diligent to carry out responsibilities.
  • Expected Outcome We are seeking an experienced professional to manage and support Waters Empower Chromatography Data System (CDS), oversee laboratory instrument integration, perform troubleshooting, and ensure system compliance with GxP and 21 CFR Part 11 regulatory requirements.
  • The role also involves Computer System Validation (CSV), administration, and continuous improvement of laboratory informatics systems.
  • Secondary Skills to be planned Post Hiring - Training Plan Strong troubleshooting, analytical, and problem-solving skills.
  • Excellent documentation, communication, and cross-functional collaboration abilities.
  • Exposure to other CDS/LIMS/ELN systems.
  • Experience in regulated environments (Pharma, Biotech, Medical Devices).
  • Familiarity with networking concepts, SQL/Oracle databases, or IT infrastructure.
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