Senior Project Manager
Group 6Barcelona, Cataluña, EspañaHace 17 días
Descripción del trabajoDegree 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.
Senior Project Manager - Biologics CDMO
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
Please apply directly or via
Seniority level : Mid‑Senior level
Employment type : Contract
Job function : Product Management
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Senior Project Manager • Barcelona, Cataluña, España