Pharma Tech Transfer Project Manager I

ThermoFisher Scientific; Monza; Presencial; EUR 52.000 - 70.000; Jornada completa

Descripción de la vacante

Thermo Fisher Scientific in Monza, Italy, seeks a Technology Transfer Project Manager to lead the introduction of new pharmaceutical products into commercial manufacturing. You will define project scope, manage timelines and document requirements.

Coordinate cross‑functional teams, communicate risks, and drive cost‑saving improvements while complying with cGMP and company procedures. A Master’s degree in a relevant field and 0–2 years GMP experience are required; the role offers an international

Formación

• Master’s degree in pharmacy, chemistry, biology, biotechnology or similar.
• 0-2 years experience within a GMP manufacturing facility or related internship experience.
• Knowledge of aseptic product manufacture is preferred.
• Basic planning and organizing skills, including risk management and technical writing skills.

Responsabilidades

• Ensure that client’s project requirements are accurately received and processed by internal functions.
• Define and supervise project scope, timing, progress and risks.
• Manage Tech Transfer interdisciplinary groups, ensuring effective task assignment and coordination.
• Coordinate the start, progress tracking, and completion of projects by staying in regular communication with team members to address and solve issues.
• Lead changes and improvements strategy for assigned project, focusing on cost savings and adherence to cGMP and company procedures.
• Contribute to team capability development, including materials management.

Conocimientos

GMP manufacturing

Project coordination

Technical writing

Risk management

Interpersonal skills

Cross-functional teamwork

Written and verbal communication

Client relationship management

Educación

Master’s degree in a relevant field

Descripción del empleo

Thermo Fisher Scientific in Monza, Italy, seeks a Technology Transfer Project Manager to lead the introduction of new pharmaceutical products into commercial manufacturing. You will define project scope, manage timelines and document requirements.

Coordinate cross‑functional teams, communicate risks, and drive cost‑saving improvements while complying with cGMP and company procedures. A Master’s degree in a relevant field and 0–2 years GMP experience are required; the role offers an international