Validation Engineer I - Medical Devices, GMP/IQ Validation

BEPC Inc. - Business Excellence Professional Consulting; Ciudad Juárez; On-site; MXN 699,056 - 961,202; Full time

Job summary

BEPC Inc. - Business Excellence Professional Consulting in Ciudad Juárez is seeking a Validation Engineer I to join its fast-growing team. This position provides technical engineering support for validation activities, ensuring compliance with GMP and regulatory requirements.

The ideal candidate will have 1-2 years of experience in the medical industry, good presentation skills, and knowledge of statistics, with an intermediate level of English. You will be responsible for executing validation activities and preparing reports.

Qualifications

• 1-2 years of experience in the medical industry.
• Intermediate English level (reading and writing) with basic conversation skills.

Responsibilities

• Provide technical engineering support for validations.
• Ensure that assigned validation activities are performed in a timely manner.
• Demonstrate sufficient knowledge in basic validation skills, GMP, and GDP.
• Responsible for the execution of validation.

Skills

Technical engineering support

Good presentation skills

Basic knowledge of statistics

Intermediate English

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.

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.

QUALIFICATIONS:

• 1-2 years 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.