Senior Validation Technician (Medical Industry)

BEPC Inc. - Business Excellence Professional Consulting; Ciudad Juárez; Presencial; MXN 300.000 - 480.000; Jornada completa

Descripción de la vacante

BEPC Inc. expands its validation team and seeks a Senior Validation Technician to support validation execution, IQ protocol development, and GMP compliance within regulated medical device environments.

The role involves providing technical support, documentation generation, and maintenance record management for validation activities, with a focus on quality and timely delivery.

Formación

• Technical title is preferred.
• 2–3 years of medical industry experience.
• Good presentation skills before groups/clients.
• Basic knowledge of statistics.
• Intermediate English reading/writing.

Responsabilidades

• Provide validation support, write IQ protocols, execute validation activities.
• Ensure validation tasks comply with GMP and GDP.
• Create forms for calibration and preventive maintenance records.
• Generate documentation and support completion reports for validations.

Educación

Engineering degree (optional)

Presentation skills

Statistics knowledge

English (reading/writing)

Herramientas

IQ protocols

GMP compliance

Descripción del empleo

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 expanding our validation team and are looking for a Senior Validation Technician with hands‑on experience in validation execution, IQ protocol development, and GMP compliance. This position will provide direct technical support for validation activities, documentation generation, and calibration and preventive maintenance records within regulated 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.

QUALIFICATIONS:

• Technical title (engineering degree is a plus)
• 2 - 3 years of experience in medical industry
• Good presentation skills before groups/clients.
• Basic knowledge of statistics.
• Intermediate English level (reading and writing).