Senior C&Q Manager - Biopharma Systems & Validation

MMR Consulting; Toluca; Presencial; MXN 1.560.603 - 2.080.804; Jornada completa

Descripción de la vacante

MMR Consulting is searching for a C&Q Manager with over 8 years of experience in the pharmaceutical and biotech industries to provide technical guidance on commissioning and qualification processes.

The role involves leading teams, managing projects, and ensuring compliance with industry standards. Responsibilities include preparing protocols, executing tests, and summarizing data while maintaining key client relationships. Strong leadership and multi-tasking skills are essential for success.

Formación

• Ability to lift 50 lbs.
• Ability to handle multiple projects in a fast-paced environment.
• Experience with preparation and execution of URS's, DQ's, FATs, SATs.

Responsabilidades

• Provide technical guidance into commissioning and qualification of equipment.
• Lead the development of qualification deliverables during the project lifecycle.
• Manage client relationships to support business development.

Conocimientos

Excellent written and spoken English

8+ years experience in commissioning, qualification or validation

Knowledge of cGMP operations

Experience with developing validation projects

Experience with upstream or downstream bioprocess equipment

Strong multi-tasking skills

Educación

Science degree or equivalent studies

Herramientas

Process control systems (PCS, SCADA)

Building automation systems

Descripción del empleo

MMR Consulting is searching for a C&Q Manager with over 8 years of experience in the pharmaceutical and biotech industries to provide technical guidance on commissioning and qualification processes.

The role involves leading teams, managing projects, and ensuring compliance with industry standards. Responsibilities include preparing protocols, executing tests, and summarizing data while maintaining key client relationships. Strong leadership and multi-tasking skills are essential for success.