Senior Project Manager

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

Descripción de la vacante

A leading biopharmaceutical company in Madrid is seeking an experienced Project Manager to lead and manage biologics and vaccine programs. The ideal candidate has over 3 years of experience in project management within the biopharmaceutical sector. Responsibilities include communication with clients, project execution, and cross-functional team facilitation. A degree in a relevant science field is required, with a preference for advanced degrees.

Formación

• 3+ years of experience in biopharmaceutical project management.
• At least 1 year in CDMO or contract manufacturing (biologics, vaccines).
• Familiarity with regulatory frameworks (EMA, FDA).

Responsabilidades

• Serve as primary point of contact for assigned clients.
• Lead end-to-end project management for biologics and vaccine programs.
• Facilitate cross-functional meetings and prepare project documentation.

Conocimientos

Project management

Communication skills

Cross-functional team leadership

Risk management

Educación

Degree in Life Sciences, Biotechnology, Pharmacy, Engineering, or related field

Master’s or PhD preferred

Descripción del empleo

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]