Engineering Project Manager

Vedi l’offerta su Go Lavoro: golavoro.it/annuncio-lavoro/7a2hdq

Experteer Overview

As an Engineering Project Manager, you will steer complex cross‑functional engineering efforts to advance mRNA process development, scale‑up, and GMP manufacturing readiness. You will coordinate Engineering, Process Development, Manufacturing, Quality, Validation, Supply Chain, Automation, and external partners to deliver compliant, on‑time outcomes. You will own strategy, timelines, budgets, risks, and governance while advancing technology transfer from development to GMP sites. This role offers visible impact on scalable biologics/drug‑product processes in a highly regulated environment. You will lead with pragmatic problem‑solving and mentor others, driving continuous improvement.

Retribuzione / Benefits

- Lead multi‑disciplinary projects spanning mRNA process development, scale‑up, tech transfer, and GMP readiness
- Coordinate cross‑functional teams across Engineering, Process Development, Manufacturing, Quality, Validation, Supply Chain, Automation, and external partners
- Define and manage project strategy, scope, timelines, budgets, resources, and risk mitigation
- Drive decision‑making, manage dependencies,



and resolve cross‑functional delivery issues
- Oversee activities related to equipment, facilities, automation, and process optimization
- Lead technology transfer activities from development to GMP manufacturing sites
- Ensure GMP, EHS, and regulatory compliance throughout the project lifecycle
- Prepare governance updates, executive summaries, and risk assessments
- Mentor junior project managers or technical staff
- Contribute to continuous improvement of project management and engineering execution

Responsabilità xysqume
- Bachelor’s or Master’s degree in Engineering, Biotechnology, Pharmaceutical Sciences, or related field
- Extensive experience managing complex engineering projects in pharma/biotech/advanced therapies
- Strong understanding of mRNA technologies, biologics manufacturing, or similar drug processes
- Proven track record in GMP‑regulated environments
- Ability to lead cross‑functional teams with autonomy and accountability
- Excellent stakeholder management, communication, and decision‑making skills

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Vedi l’offerta su Go Lavoro: golavoro.it/annuncio-lavoro/7a2hdq