Senior Validation Engineer (Medical Industry)

BEPC Inc. - Business Excellence Professional Consulting; Ciudad Juárez; On-site; MXN 500,000 - 800,000; Full time

Job summary

BEPC Inc. Mexico, a division of BEPC Incorporated, seeks a Senior Validation Engineer to lead validation strategies in regulated medical device environments. You will execute IQ/OQ/PQ, CSV, TMV, and SAT protocols, run DOEs, and apply Lean and Six Sigma methodologies while ensuring GMP/GDP compliance.

The role emphasizes planning through execution, data-driven validation, and collaboration with cross-functional teams in automotive and medical device contexts.

Qualifications

• Engineering degree; master's degree is a plus.
• 4–5 years of experience in medical industry.
• Solid skills in developing Factorial Experiments (DOE).
• Extensive knowledge in Lean.
• Intermediate knowledge in Six Sigma, DMAIC and Kaizen.
• Intermediate knowledge of Project Management.

Responsibilities

• Lead validation strategies and execute IQ/OQ/PQ and CSV protocols.
• Execute TMV and SAT validation activities and support completion reports.
• Perform pre-validation experiments and other needed tests.
• Ensure GMP and GDP compliance across validation activities.
• Create calibration and preventive maintenance records documentation.

Skills

DOE development

Lean

Six Sigma (DMAIC)

Project management

Presentation skills

Education

Engineering Degree

Master’s in science (plus)

Job description

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 Senior Validation Engineer with deep expertise in process, equipment, and computer systems validation, including IQ/OQ/PQ, CSV, TMV, and SAT. This role will lead validation strategies, execute Design of Experiments (DOE), apply Lean and Six Sigma methodologies, and support validation projects from planning through execution in regulated medical device environments.

KEY RESPONSIBILITIES:

• 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.
• Provide technical engineering support for validations, write, and execute Test Method Validation (TMV) protocols.
• Provide technical engineering support for validations, write, and execute SAT (Factory Acceptance Testing) validation protocols, and provide data to write completion reports for assigned validations.
• Responsible for running experiments during the pre-validation phase, run 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.

QUALIFICATIONS:

• Engineering Degree (master’s in science is a plus)
• 4 – 5 years of experience in medical industry
• Good presentation skills before groups/clients.
• Solid skills in developing Factorial Experiments (DOE).
• Extensive knowledge in Lean.
• Intermediate knowledge in Six Sigma, DMAIC and Kaizen.
• Intermediate knowledge of Project Management.