QC Team Lead — GMP Analytics & Leadership

UNAVAILABLE; Loures; Presencial; EUR 42.000 - 54.000; Jornada completa

Descripción de la vacante

Hovione in Loures, Portugal, is looking for a Laboratory Supervisor to oversee daily QC operations on the shift, ensuring GLP, GMP and HSE compliance, and maintaining readiness of equipment, records and logbooks across the batch cycle. You will coordinate resources, monitor timelines and promote a culture of Excellence and Right First Time.

You will lead and coach the team, support investigations of OOS/OOT deviations, ensure data integrity, and collaborate with Quality Control Managers to

Formación

• GMP and QC laboratory experience in pharmaceutical industry.
• Strong analytical theory and techniques understanding.
• Ability to lead and allocate resources.
• Excellent written and verbal communication; shift-based collaboration.
• Proficient with MS Office and digital tools.

Responsabilidades

• Supervise, execute, and evaluate daily laboratory operations during the assigned shift, ensuring GLP, GMP, and HSE requirements.
• Ensure safe working conditions and laboratory readiness through assessment of tidiness, equipment status, and corrective actions prior to shift handover.
• Plan, prioritize, and allocate workload, samples, and equipment to shift team members based on proficiency, training, and operational priorities.
• Monitor sample flow, critical timelines, system suitability, and equipment performance, adjusting operations as needed to meet Production requirements.
• Promote a culture of Excellence, Right First Time execution, productivity, flexibility, and on-time delivery of accurate analytical results.
• Communicate effectively with Quality Control Managers through routine alignment meetings, escalation of bottlenecks, and shift handovers.
• Monitor and document adherence to the established plan, ensuring deviations are justified, investigated, and communicated to subsequent shifts.
• Ensure data integrity and compliance of all analytical activities, records, logbooks, calibrations, and equipment maintenance in line with GMP standards.
• Support investigations of OOS/OOT/atypical results, deviations, and QC incidents, including follow-up of corrective and preventive actions.
• Train, coach, and support team members, identify training needs, contribute to performance reviews, and support onboarding and induction activities.

Conocimientos

Leadership

Problem solving

Communication

Laboratory operations

GMP QC knowledge

Educación

High School diploma

Chemistry/Analytical Chemistry/Chemical Engineering/Pharmaceutical Sciences (related)

Herramientas

MS Office

MS Teams

Descripción del empleo

Hovione in Loures, Portugal, is looking for a Laboratory Supervisor to oversee daily QC operations on the shift, ensuring GLP, GMP and HSE compliance, and maintaining readiness of equipment, records and logbooks across the batch cycle. You will coordinate resources, monitor timelines and promote a culture of Excellence and Right First Time.

You will lead and coach the team, support investigations of OOS/OOT deviations, ensure data integrity, and collaborate with Quality Control Managers to