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.
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 / Qualifications
* 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.
Seniority level
* Mid-Senior level
Employment type
* Contract
Job function
* Product Management
Industries
* Biologics
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