Senior C&Q Engineer - Biopharma GMP Validation Lead

MMR Consulting; Ciudad de México; Presencial; MXN 1.375.043 - 2.062.564; Jornada completa

Descripción de la vacante

MMR Consulting in Mexico is seeking a Sr. C&Q Engineer with over 12 years of experience in the pharmaceutical and biotech industries. The successful candidate will lead commissioning and qualification efforts for various systems, ensuring compliance with cGMP regulations. This role requires strong leadership and mentoring skills as well as a solid background in validating biopharmaceutical processes.

Candidates should hold an engineering degree and have experience with biotech process equipment. Travel may be required and TN Visa sponsorship is offered.

Formación

• 12+ years of experience in commissioning, qualification, or validation in pharma/biotech.
• Strong understanding of cGMP operations and validation methodologies.
• Experience with biotech process equipment such as fermentation and chromatography.

Responsabilidades

• Lead commissioning and qualification of pharmaceutical process equipment.
• Develop key qualification deliverables during the project lifecycle.
• Mentor junior engineers while leading teams on complex projects.

Conocimientos

Leadership skills

Strong multi-tasking skills

Pharmaceutical/Biotech experience

Educación

Engineering degree (Mechanical, Electrical or Chemical)

Herramientas

cGMP process equipment

PCS, SCADA, Historians

Descripción del empleo

MMR Consulting in Mexico is seeking a Sr. C&Q Engineer with over 12 years of experience in the pharmaceutical and biotech industries. The successful candidate will lead commissioning and qualification efforts for various systems, ensuring compliance with cGMP regulations. This role requires strong leadership and mentoring skills as well as a solid background in validating biopharmaceutical processes.

Candidates should hold an engineering degree and have experience with biotech process equipment. Travel may be required and TN Visa sponsorship is offered.