Senior Project Manager

QP Group; Barcelona; Presencial; EUR 50.000 - 70.000; Jornada completa

Descripción de la vacante

A global Biologics CDMO near Barcelona is seeking a Senior Project Manager to lead client projects in biologics and vaccines. The successful candidate will manage project execution, ensuring quality and compliance with GMP standards. Requirements include a relevant degree, at least 3 years in biopharmaceutical project management, and ability to work in a fast-paced environment. Interested applicants can apply directly or via email.

Formación

• 3+ years of experience in biopharmaceutical project management.
• At least 1 year in CDMO or contract manufacturing.
• Familiarity with process development, analytical methods, and regulatory frameworks.

Responsabilidades

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

Conocimientos

Project management

Cross-functional team leadership

Communication skills

Risk management

Educación

Degree in Life Sciences, Biotechnology, Pharmacy, or Engineering

Master’s or PhD preferred

Descripción del empleo

Overview

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.

Please apply directly or via [e-mail]