Validation Engineer I

BEPC Inc. - Business Excellence Professional Consulting; Ciudad Juárez; Presencial; MXN 180.000 - 240.000; Jornada completa

Descripción de la vacante

BEPC Inc. in Ciudad Juárez is seeking a Validation Engineer I to provide technical engineering support for validation activities in manufacturing and medical device environments, ensuring GMP/GDP compliance.

The role involves IQ protocol development, executing validations, and preparing validation reports, with an emphasis on data integrity, basic statistics, and clear documentation. 1–3 years in manufacturing or 1 year in the medical industry; intermediate English; strong presentation skills;

Formación

• 1–3 years of experience in manufacturing and/or 1 year in medical industry.
• Good presentation skills before groups/clients.
• Basic knowledge of statistics.
• Intermediate English level (reading and writing) with basic conversation skills.

Responsabilidades

• 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 GMP.
• Demonstrate sufficient knowledge in basic validation skills, GMP, GDP.

Conocimientos

Validation

IQ protocol development

GMP/GDP knowledge

English proficiency

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.

BEPC Inc. is seeking a Validation Engineer I to join our fast-growing team of consultants in the Ciudad Juárez 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.

MAIN QUALIFICATIONS:

• 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.