Process Scientist I, Manufacturing Sciences

Work Schedule
Standard (Mon-Fri)

Environmental Conditions
Office

Job Description

Thermo Fisher Scientific Inc. is the world leader in serving science, with annual revenue of more than $40 billion. Our Mission is to enable our customers to make the world healthier, cleaner and safer. Whether our customers are accelerating life sciences research, solving complex analytical challenges, growing efficiency in their laboratories, improving patient health through diagnostics or the development and manufacture of life-changing therapies, we are here to support them. Our distributed team delivers an outstanding combination of innovative technologies.

We are seeking a highly motivated candidate for the role of Process Scientist II in the PDS team in Monza (Italy). The position requires expertise in manufacturing and process technology to address various challenge related to the Pharma Clinical Manufacturing and Commercial.

Key Responsibilities:

As Scientist, you will chip into the definition, development, improvement, and transfer of sterile products to cGMP PDS suites of Monza site. You will draft the manufacturing process chart in accordance with the product quality target profile, product knowledge and development data as well as write clear and professional protocol to support timely project completion. As SME of process, you will ask to support scale-up of lab-scale processes and technology transfer to the cGMP manufacturing for clinical and commercial batches. Discussing the progress of activities and propose technical solutions with internal and external partners is crucial.

Should also be able to analyze, interpret, and present results to project teams, and write technical reports.

Qualifications:

B.S or M.S. in Medicinal Chemistry/Chemistry/Chemical Engineering/Biotechnology, Pharmaceutical Chemistry and Technology, Pharmacy or related scientific subject areas with meaningful expertise in pharma industry.

Requirements:

Proven experience in development and manufacturing of sterile products, liquid, suspension and lyophilized products

Experience with GLP and GMP compliance and manufacturing preferred.

Experience writing content for technical documentation as work instructions, study protocols and reports, FMEA, GAP Analysis

A high level of dedication and a track record of quality work, with attention to detail.

Capable of presenting the work clearly to Clients and Team.

Ability to multi-task and prioritize to meet important achievements.

Maintaining up-to-date in new technologies and scientific literature to drive innovation.

Critical thinking and curiosity.

A self-starter and outstanding teammate.

Excellent written and spoken English.

Thermo Fisher Scientific is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, creed, religion, color, national or ethnic origin, citizenship, sex, sexual orientation, gender identity and expression, genetic information, veteran status, age or disability status.

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