Validation Lead at Katalyst Healthcares Life Sciences
Raritan, NJ 08869, USA -
Full Time


Start Date

Immediate

Expiry Date

11 Sep, 25

Salary

0.0

Posted On

12 Jun, 25

Experience

3 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Good communication skills

Industry

Information Technology/IT

Description

Roles & Responsibilities:

  • Minimum 3+ years’ experience with SAP or Blue Yonder Warehouse Management Systems.
  • 3+ years’ experience with System Development Lifecycle.
  • 3+ years’ experience in Computer System Validation.
  • Experience with FDA CSA principles Experience with J&J CSV Framework Experience in FDA and/or Global regulated environment with good understanding of GxP standards and Risk based validation.
  • Knowledge of FDA guidance and industry standards (i.e., GAMP) Experience in writing and executing documentation for all aspects of the validation deliverables (etc. Requirements, Compliance/validation Plans, test protocols, Test Summary reports and Compliance/Validation Reports.
  • Experience in reviewing system test and user acceptance test scripts, Traceability matrix and Design Specs. Experience in QA Methodologies, designing, reviewing and approving Test Plans, systems and UAT test scripts and Test procedures.
  • Strong verbal and written communication skills.
  • Ability to work as a team player, lead a team or accomplish tasks without supervision.
  • Ability to work with remote teams and support several changes/projects simultaneously.
  • Ability to provide Validation guidance, timely reviews, and escalations to TQ management.
Responsibilities
  • Minimum 3+ years’ experience with SAP or Blue Yonder Warehouse Management Systems.
  • 3+ years’ experience with System Development Lifecycle.
  • 3+ years’ experience in Computer System Validation.
  • Experience with FDA CSA principles Experience with J&J CSV Framework Experience in FDA and/or Global regulated environment with good understanding of GxP standards and Risk based validation.
  • Knowledge of FDA guidance and industry standards (i.e., GAMP) Experience in writing and executing documentation for all aspects of the validation deliverables (etc. Requirements, Compliance/validation Plans, test protocols, Test Summary reports and Compliance/Validation Reports.
  • Experience in reviewing system test and user acceptance test scripts, Traceability matrix and Design Specs. Experience in QA Methodologies, designing, reviewing and approving Test Plans, systems and UAT test scripts and Test procedures.
  • Strong verbal and written communication skills.
  • Ability to work as a team player, lead a team or accomplish tasks without supervision.
  • Ability to work with remote teams and support several changes/projects simultaneously.
  • Ability to provide Validation guidance, timely reviews, and escalations to TQ management
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