Validation Engineer I

BEPC Inc. - Business Excellence Professional Consulting; Chihuahua; Presencial; MXN 180.000 - 280.000; Jornada completa

Descripción de la vacante

BEPC Inc. in Ciudad Juárez is seeking a Validation Engineer I to join our engineering team. The role supports validation activities in manufacturing and medical device environments, ensuring GMP/GDP compliance and proper documentation.

IQ protocol development and validation report preparation are key parts of the job. The candidate should hold an engineering degree, have 1–3 years in manufacturing or 1 year in medical devices, and possess intermediate English skills.

Formación

• Engineering degree required.
• 1–3 years in manufacturing; or 1 year in medical industry.
• Good presentation skills before groups/clients.
• Basic knowledge of statistics.
• Intermediate English reading/writing; 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 validation activities are performed in a timely manner and in accordance with GMP and GDP requirements.
• Demonstrate knowledge in basic validation skills, GMP, GDP, and Good Documentation Practices.

Conocimientos

English (intermediate)

Presentation skills

Basic 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.

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:

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.