Una candidatura completa en un minuto: currículum y carta de presentación adaptados, listos para enviar.
Mentor Technical Group seeks a detail-oriented Documentation Specialist to support cGMP-compliant activities for pharmaceutical and life sciences projects. You will manage technical documentation, ensure regulatory compliance, and contribute to ISO 17025:2017 standards while collaborating with MTG teams to meet client expectations.
Responsibilities include maintaining quality records, reviewing procedures, and supporting audits; you will also coordinate with supervisors to ensure timely delivery
Mentor Technical Group seeks a detail-oriented Documentation Specialist to support cGMP-compliant activities for pharmaceutical and life sciences projects. You will manage technical documentation, ensure regulatory compliance, and contribute to ISO 17025:2017 standards while collaborating with MTG teams to meet client expectations.
Responsibilities include maintaining quality records, reviewing procedures, and supporting audits; you will also coordinate with supervisors to ensure timely delivery