Ingeniero de Validacion I

BEPC Inc. - Business Excellence Professional Consulting

Monterrey

On-site

MXN 260,000 - 460,000

Full time

4 days ago
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Job summary

BEPC Inc. is seeking a Validation Engineer I to join our fast-growing team of consultants in Apodaca, Nuevo Leon area.

The role provides technical engineering support for validation activities, ensuring compliance with GMP, GDP, and current regulatory requirements. The role involves supporting IQ protocol development, execution of validation activities, and preparation of validation reports within manufacturing and medical device environments.

Qualifications

  • Engineering degree required.
  • Knowledge of GMP and GDP.
  • Basic statistics knowledge.

Responsibilities

  • Provide technical engineering support for validations, may write IQ validation protocols, execute validation activities, and provide data to write completion reports for assigned validations.
  • Ensure that assigned validation activities are performed in a timely manner and in accordance with current requirements and GMP.

Skills

GMP knowledge
GDP knowledge
Good Documentation Practices
Basic statistics
Intermediate English

Education

Engineering Degree

Tools

IQ Protocols
Validation reports

Job description

BEPC Inc. is seeking a Validation Engineer I to join our fast-growing team of consultants in Apodaca, Nuevo Leon area.

This position provides technical engineering support for validation activities, ensuring compliance with GMP, GDP, and current regulatory requirements.

The role involves supporting IQ protocol development, execution of validation activities, and preparation of validation reports within manufacturing and medical device environments.

KEY RESPONSIBILITIES:
  • Provide technical engineering support for validations, may write Installation Qualification (IQ) validation protocols, execute validation activities, and provide data to write completion reports for assigned validations.
  • 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 basic 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.
  • Engineering Degree. 1 - 3 years of experience in the manufacturing industry and/or 1 year of experience in medical industry Good presentation skills before groups/clients.
  • Basic knowledge of statistics.
  • Intermediate English level (reading and writing) with basic conversation skills.
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