MSAT Scientist: Process Engineering & Project Lead

Johnson & Johnson Innovative Medicine; Borgo San Michele; On-site; EUR 30,000 - 49,000; Full time

Benefits offered by this job

Annual bonus

Vacation days

Parental leave

Job summary

Johnson & Johnson Innovative Medicine, Latina, Italy, is seeking an MSAT Assistant Scientist to oversee project planning and cross-functional collaboration within pharmaceutical manufacturing. You will coordinate multi-department efforts to ensure project success and timely execution of activities.

The role requires identifying risks, defining mitigation strategies, and ensuring compliance with GMP, quality, and safety standards.

Qualifications

• Master’s degree in Engineering, Pharmacy, CTF or Chemistry is required.
• At least 6 months experience in the pharmaceutical industry (Oral Solid production preferred).
• Academic knowledge of lines, processes, materials and equipment for pharmaceutical processes.
• Good knowledge of quality, compliance and GMP related to manufacturing and packaging of pharmaceutical products.
• Basic experience in Project Management.
• Ability to coordinate cross-functional teams to meet timelines.
• Fluent in English (B2 level and above).

Responsibilities

• As Project Leader, ensure planning and coordination of activities with involved departments.
• Identify risks and define mitigation strategies.
• Assess business impact, quality, compliance and safety with stakeholders.
• Ensure timely communication to MSAT Supervisor and Global Functions.
• Ensure timely availability of quality documentation for project execution.
• Perform and/or support investigations for non-conformances.
• Collaborate with Data Science for Process Analytical Technologies and chemometrics usage.

Skills

English fluency

Project management

Cross-functional coordination

Problem solving

Education

Master’s degree in Engineering, Pharmacy, CTF or Chemistry

Job description

Johnson & Johnson Innovative Medicine, Latina, Italy, is seeking an MSAT Assistant Scientist to oversee project planning and cross-functional collaboration within pharmaceutical manufacturing. You will coordinate multi-department efforts to ensure project success and timely execution of activities.

The role requires identifying risks, defining mitigation strategies, and ensuring compliance with GMP, quality, and safety standards.