Senior Project Manager (Digital)

QP Group; Madrid; Presencial; EUR 70.000 - 90.000; Jornada completa

Descripción de la vacante

A major biotechnology firm located near Barcelona is seeking a Senior Project Manager to lead cross-functional client projects in biologics and vaccines. The successful candidate will manage project execution, ensuring compliance with GMP standards and delivering high-quality results. A Master's or PhD and at least 3 years of project management experience in the biopharmaceutical sector are required. This role offers competitive compensation and an opportunity to contribute to innovative healthcare solutions.

Formación

• 3+ years of experience in biopharmaceutical project management.
• At least 1 year in CDMO or contract manufacturing.
• Experience managing GMP manufacturing or tech transfer projects.

Responsabilidades

• Lead end-to-end project management for biologics and vaccine programs.
• Translate customer requirements into actionable project plans.
• Drive project execution according to scope, schedule, and budget.

Conocimientos

Project management

GMP knowledge

Cross-functional leadership

Risk management

Educación

Master’s or PhD

Descripción del empleo

QP Group is partnered with a global Biologics CDMO with a facility near Barcelona who are actively looking to add a Senior Project Manager to their team. They want the successful candidate to lead cross-functional client projects, ensuring delivery of high-quality biologics and vaccines under GMP conditions.

Lead end-to-end project management for biologics and vaccine programs — from process development and tech transfer to GMP manufacturing, QC, and release.

Translate customer requirements into actionable project plans, aligning internal functions (Process Development, QA / QC, Regulatory, Operations, Supply Chain).

Drive project execution according to scope, schedule, and budget while proactively managing risks and change controls.

Facilitate cross-functional meetings, prepare project documentation (Gantt charts, dashboards, risk logs), and maintain regular project reporting.

Master’s or PhD preferred.

~3+ years of experience in biopharmaceutical project management, with at least 1 year in CDMO or contract manufacturing (biologics, vaccines, cell & gene therapy, or injectables).

~ Demonstrated success in managing GMP manufacturing or tech transfer projects.