Senior C&Q Engineer - Biopharma Validation Lead (Toluca de Lerdo)

Overview

MMR Consulting is seeking a Sr. C& Q Engineer based in Toluca, Mexico, to lead teams for client projects in the biopharmaceutical sector. The successful candidate will have over 12 years of experience in commissioning, qualification, and validation, particularly in c GMP environments.

Responsibilities

• Provide technical guidance on commissioning, qualification, and validation activities.
• Develop qualification deliverables and ensure alignment with industry standards.
• Lead teams on client projects and mentor junior team members.
• Manage multiple projects concurrently while maintaining quality and timelines.

Qualifications

• 12+ years of experience in commissioning, qualification, and validation, particularly in c GMP environments.
• Strong leadership and mentorship skills.
• Ability to manage multiple projects concurrently and work in a client-service context.