Senior Validation Technician (Medical Industry)

Bepc Inc. - Business Excellence Professional Consulting; Chihuahua; On-site; MXN 360,000 - 480,000; Full time

Job summary

BEPC Inc. in Mexico is seeking a Senior Validation Technician to join our expanding validation team in Chihuahua. You will perform validation execution, IQ protocol development, and GMP/GDP compliance support in regulated manufacturing and medical device environments.

You will provide direct technical support for validation activities, generate documentation, calibrations, and preventive maintenance records, and ensure timely completion of validations per current requirements.

Qualifications

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

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 GMP.
• Demonstrate knowledge in basic validation skills, GMP, GDP. Responsible for execution of validation, including creation of forms for calibration and preventive maintenance records.

Skills

Validation

IQ Protocols

GMP

GDP

English

Presentation

Education

Engineering Degree

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 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).