Senior Pharma C&Q Engineer | Lead Validation & Start-up

MMR Consulting; Tijuana; On-site; MXN 1,387,203 - 2,080,804; Full time

Job summary

MMR Consulting is seeking a Sr. C&Q Engineer in Tijuana, Mexico, to lead teams in the validation of biopharmaceutical systems and equipment. With a focus on commissioning and qualification, the role includes technical guidance, project management, and mentorship of junior engineers.

The successful candidate should have over 12 years of relevant experience in the pharmaceutical/biotech industry and possess a degree in Engineering. MMR Consulting offers a supportive environment with opportunities for professional growth.

Qualifications

• 12+ years of experience in the pharmaceutical/biotech industry.
• Knowledge of cGMP operations.
• Ability to lift 50lbs.

Responsibilities

• Provide technical guidance in commissioning and qualification.
• Lead development of qualification deliverables.
• Support Project Validation Plans development.

Skills

Leadership skills

Experience in commissioning, qualification or validation

Strong multi-tasking skills

Ability to handle multiple projects

Education

Engineering degree (Mechanical, Electrical or Chemical)

Tools

PCS, SCADA

Biotech process equipment

Job description

MMR Consulting is seeking a Sr. C&Q Engineer in Tijuana, Mexico, to lead teams in the validation of biopharmaceutical systems and equipment. With a focus on commissioning and qualification, the role includes technical guidance, project management, and mentorship of junior engineers.

The successful candidate should have over 12 years of relevant experience in the pharmaceutical/biotech industry and possess a degree in Engineering. MMR Consulting offers a supportive environment with opportunities for professional growth.