Senior Validation Technician

BEPC Inc. - Business Excellence Professional Consulting; Ciudad Juárez; Presencial; MXN 420.000 - 640.000; Jornada completa

Descripción de la vacante

BEPC Inc. Mexico, a division of BEPC Incorporated, is expanding its validation team and seeks a Senior Validation Technician to support validation activities in regulated manufacturing and medical device environments.

The role involves IQ protocol development, execution of validation tasks, and documentation generation. Ideal candidates have 3–5 years in manufacturing or 2–3 years in the medical industry, with intermediate English and basic statistics knowledge.

Formación

• Engineering degree preferred; technical title is a plus.
• 3–5 years of experience in manufacturing and/or 2–3 years in the medical industry.
• Good presentation skills before groups/clients.
• Basic knowledge of statistics.
• Intermediate English (reading and writing).

Responsabilidades

• Provide technical engineering support for validations, may write IQ validation protocols, execute validation activities, and provide data for completion reports.
• Ensure validations are performed timely and in accordance with GMP.
• Demonstrate knowledge in basic validation skills, GMP, GDP.
• Execute validation, including the creation of forms to create calibration and preventive maintenance records.

Conocimientos

Validation

Presentation skills

Statistics knowledge

Educación

Engineering degree

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.

MAIN QUALIFICATIONS:

• Technical title (engineering degree is a plus)
• 3 - 5 years of experience in the manufacturing industry and/or 2 - 3 years of experience in medical industry
• Good presentation skills before groups/clients.
• Basic knowledge of statistics.
• Intermediate English level (reading and writing)