CSV Engineer

Katalyst HealthCares and Life Sciences

$90K — $130K *
US-AnywhereRemote in Raritan, NJ
Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • 7-10 years of experience in CSV and GxP compliance validation activities across the SDLC.
  • Proven experience with Manufacturing, MES, and Data Platform Applications in GxP settings.
  • Deep understanding of FDA and global regulations related to GxP compliance.
  • Strong skills in validation documentation, including compliance plans, test protocols, and reports.
  • Demonstrated expertise in risk-based validation and risk management principles.
  • Effective leadership skills to mentor and guide cross-functional teams.
  • Experience with Agile tools such as Jira, Xray, or qTest.
  • Strong verbal and written communication skills in English.

Responsibilities

  • Lead validation activities for GxP systems with minimal supervision.
  • Support global and regional GxP computerized systems in manufacturing environments.
  • Review and ensure compliance of validation documentation and deliverables.
  • Apply risk management practices in validation activities.
  • Coordinate projects while communicating status, risks, and issues to stakeholders.
  • Write and maintain various compliance documentation, including test plans and procedures.
  • Foster collaborative partnerships across teams to support business objectives.

Benefits

  • Opportunities for professional development and mentorship.
  • Collaboration with cross-functional and external teams.
  • Support for global GxP compliance initiatives.
  • Work with leading-edge technology and tools.
Full Job Description
Summary :

Roles & Responsibilities :

  • Strong CSV and Quality expertise with ability to independently lead validation activities across the SDLC for GxP systems with minimal supervision. 7-10 years of relevant experience.
  • Proven experience with Manufacturing, MES, and Data Platform Applications, including support for global and regional GxP computerized systems.
  • Deep knowledge of GxP compliance, FDA/Global regulations, and Inspection Readiness.
  • Expertise in validation documentation and deliverables, including review of compliance plans, requirements, design specs, test protocols, test scripts, defects, traceability, reports and system procedures.
  • Demonstrated application of risk-based validation and risk management practices.
  • Effective leadership and mentoring skills, guiding cross-functional and external teams (Senior and Junior consultants).
  • Strong project coordination and stakeholder communication skills, including managing risks, issues, and status reporting.
  • Experience in writing documentation (i.e. Compliance Plan, Test Plans, Test Reports, Compliance Summary Reports, and SOPs).
  • Knowledge of Agile Tools (e.g., Jira, Xray, qTest, etc.).
  • bility to build collaborative partnerships, work as a team player and support execution of business objectives across teams, including timely escalations to TQ manager.
  • Primary Language required: English. Strong verbal and written communication skills.
  • bility to work with dispersed/remote teams and support several projects simultaneously.
  • Experience with Acquisitions/Separations/ Divestiture efforts is desirable.

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