Manufacturing Science level II

Thermo Fisher Scientific Inc.; Milano; Ibrido; EUR 35.000 - 55.000; Tempo pieno

Descrizione del lavoro

Thermo Fisher Scientific Inc. is seeking a Manufacturing Science level II professional in Milan to contribute to impactful projects. This role involves technology transfer activities, documentation preparation adhering to GMP, and serving as a liaison with clients. Candidates should have a degree in a relevant field and experience in pharmaceutical manufacturing.

Competenze

• Degree or equivalent experience in Chemistry, Engineering.
• 3 years experience in a pharmaceutical environment.
• Knowledge of filling processes in syringes and cartridges is a must.

Mansioni

• Handle technology transfer activities to the manufacturing department.
• Support scheduling of manufacturing activities.
• Prepare process documentation adhering to GMP requirements.

Conoscenze

GMP knowledge

Leadership

Teamwork

Formazione

Degree in Chemistry or Engineering

Strumenti

IT software proficiency

Descrizione del lavoro

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

Manufacturing Science level II

Join Thermo Fisher Scientific Inc., where your work will contribute to impactful projects, such as finding cures for cancer, protecting the environment, and ensuring food safety. Located at our Ferentino site in Italy, this role within our Manufacturing Sciences division offers you the chance to be part of an ambitious and world-class team!

How will you make an impact?

• Handle technology transfer activities to the manufacturing department by selecting appropriate process materials and establishing the manufacturing process.
• Support the production department to ensure flawless scheduling of manufacturing activities.
• Serve as the reference contact for our clients on process-related topics.

A day in the life

• Follow tech transfer projects from the kickoff meeting with the client through the entire lifecycle of the project.
• Prepare process documentation to support manufacturing activities, respecting project achievements and adhering to GMP requirements and internal SOPs.
• Provide appropriate training to production personnel responsible for manufacturing activities according to MBR instructions.
• Communicate with clients about technical aspects relevant to the project, providing updates on project activities.
• Collaborate with the Formulation Development laboratory to develop studies that define the GMP process.

How will you get here?

• Degree or equivalent experience in CTF, Chemistry, Engineering with previous experience of 3 year in a pharmaceutical environment.
• Experience in the development and manufacturing process of lyophilized and liquid sterile products.
• Knowledge of filling processes in syringes and cartridges is a must.

Knowledge, Skills, Abilities

• GMP knowledge
• Proficiency with main IT software
• Leadership and independence in handling tasks
• Strong teamwork capabilities