Senior Project Manager

Group 6; Santiago de Compostela; Presencial; EUR 60.000 - 80.000; Jornada completa

Descripción de la vacante

A leading biotechnology firm located near Barcelona is seeking a Senior Project Manager to lead cross-functional client projects in the biologics sector. The role involves end-to-end project management for high-quality biologics and vaccines under GMP conditions. The ideal candidate will have over 3 years of biopharmaceutical project management experience and a degree in a related field. This role offers competitive compensation and the chance to make significant contributions to the field.

Formación

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

Responsabilidades

• Serve as primary contact for CDMO clients.
• Lead end-to-end project management for biologics and vaccines.
• Drive project execution according to scope, schedule, and budget.

Conocimientos

Project management

Communication

Risk management

Cross-functional team leadership

Educación

Degree in Life Sciences, Biotechnology, Pharmacy, or Engineering

Master's or PhD preferred

Descripción del empleo

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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.

Responsibilities

• Serve as primary point of contact for assigned CDMO clients, ensuring transparent and effective communication.
• 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.

Experience Required

• Degree in Life Sciences, Biotechnology, Pharmacy, Engineering, or related field; 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.
• Familiarity with process development, analytical methods, and regulatory frameworks (EMA, FDA).
• Proven ability to manage cross‑functional teams in a matrixed, fast‑paced environment.

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