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Staff Software Validation Engineer

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Onsite

Staff Software Validation Engineer

BEPC Inc. - Business Excellence Professional Consulting

Staff Software Validation Engineer

2 months ago

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Important information


Contract type:

Permanent

Location:

Ciudad Juárez, Chihuahua, Mexico

Work mode:

Onsite

Published on:

31 August 2026

What they need


BEPC Inc. provides Specialized Engineering Solutions and IT Project Management services to Fortune 500 companies in the Life Science and Technology industries. BEPC Mexico, a division of BEPC Incorporated, provides and manages consulting services for Automotive and Medical device companies throughout Mexico and around the globe.

At BEPC Inc., we are looking for a Staff Software Validation Engineer (CSV) with deep expertise in end-to-end validation strategies, including process, equipment, computer systems, and maintenance validations. This role will lead DOE development, Lean Six Sigma initiatives, and project-level execution, while collaborating closely with Operations, Design, and Engineering teams to ensure products meet regulatory, quality, and design requirements.

RESPONSABILITIES:

  • Responsible for leading and ensuring on-time execution of Continuous Improvement Workstream #2 active projects as per commitment and plan.
  • Execute and generate moderate to high complex validation documentation.
  • Responsible for communicating and keeping track of the activities at the DTx Core Team, site leadership, business leadership stakeholders.
  • Responsible of updating and keeping track of the project's metrics, weekly updates and site dashboards (PO Tracker, Project Timelines, Validation Documentation Tracker, Risk Register and KPI Tracker).
  • Provide training sessions for team members and stakeholders on validation processes and tools.
  • Create and submit Change Projects & Change Orders (COs) ensuring proper documentation and approval processes are followed.
  • Collaborate with team members to gather requirements and feedback for validation of documentation and training materials.
  • Monitor and report on the status of validation activities and Change Orders to the project lead, site leadership and business leadership stakeholders.
  • Provide technical engineering support for validations, write, and execute Installation Qualification (IQ) protocols, and provide data to write completion reports for assigned validations.
  • Provide technical engineering support for validations, write, and execute Operational Qualification (OQ) protocols, and provide data to write completion reports for assigned validations.
  • Provide technical engineering support for validations, write, and execute Performance Qualification (PQ) protocols, and provide data to write completion reports for assigned validations.
  • Provide technical engineering support for validations, write, and execute Computer Systems Validation (CSV) protocols.
  • Responsible for running experiments during the pre-validation phase, running other experiments as needed.
  • Ensure that assigned validation activities are performed in a timely manner and in accordance with current requirements and Good Manufacturing Practices (GMP).
  • Demonstrate sufficient knowledge in validation skills, GMP, Good Documentation Practices (GDP).
  • Responsible for the execution of validation, including the creation of forms to create calibration and preventive maintenance records.
  • Support for the development of the production of new products.
  • Responsible for the analysis and development of manufacturing functions, capabilities and facilities necessary to produce the client's product.
  • Work with the Operations and Design team to verify and validate that the product under development meets regulatory and design requirements.

QUALIFICATIONS:

  • Engineering Degree (master’s in science is a plus)
  • 6 – 9 years of experience in medical industry
  • Expert with LIMs or Expert in connecting equipment's to LIMs software
  • Expert with Software Validation
    • should be able to draft, approve Software Validation documents - like URS, Test Protocol, Computer specifications etc.
  • Expert with working/collaborating Cross functional departments, multiple suppliers.
  • Expert with MS project, Project Management
    • be able to Manage/track action plans for multiple equipment validation
  • Good presentation skills before groups/clients.
  • Solid skills in developing Factorial Experiments (DOE).
  • Bilingual

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