Scientist

3 settimane fa

Siena, Italia GSK A tempo pieno

**Site Name**: Italy - Siena

**Posted Date**: Jul 20 2023
**Scientist**

We’re combining the power of genetic and genomic insights into what causes disease, with the speed and scale of artificial intelligence and machine learning (AI/ML) to make better predictions about who a treatment might work for, and why. We believe this powerful combination of data and technology holds the key to fundamentally transforming medical discovery for the better, improving R&D success rates and shaping how even the most challenging diseases, like neurological conditions and cancer, can be both prevented and treated.

**Job Purpose**:
We are seeking a highly motivated, enthusiastic and skilled lab-based scientist to join our Global Process Engineering Drug Product team, based in Siena, Italy. Our goal is to deliver and transfer stable vaccine formulations and robust processes (fill & finish) to the clinical and manufacturing sites within GSK network.

The Scientist is expected to design and execute scientific studies in support of technical programs as they progress from early development into Phase I/ II, Phase III, technology transfer and process performance qualification at the intended commercial site.

**Key Responsibilities**:

- Provide knowledge of principles and concepts to define process understanding activities for vaccines at different development stages following the Quality by Design (QbD) framework.
- Participate in drug product development programs where you will design, conduct, interpret, and present the results of process development studies.
- Support the Technical Transfer of the drug product manufacturing process to the GMP production facilities
- Author and review technical protocols and reports on projects at various development stages, also in support of Regulatory submissions
- Generate strong relationships in the area of technical development with high quality partners beneficial to the organization, both internally and externally, to strength development/implementation of new methods/technologies (i.e. PAT).
- Execute scientific and technical activities to support the production of vaccine trial material to be used in GLP non-clinical safety studies

**_ Why you? _**

**Basic Qualifications & Skills**:

- Degree in Chemical Engineering, Chemistry, Biotechnology, Pharmaceutical Science, or related scientific fields.
- Good understanding of vaccine/biopharma manufacturing process.
- Fluent in spoken and written in English
- Ability to work with cross-functional teams and communicate effectively
- Learning agility, be proactive and self-motivated

**Preferred Qualifications & Skills**:

- Experience in technology transfer and industrialization is an asset
- Previous experience in supporting process development of parental drug product

GSK is a global biopharma company with a special purpose - to unite science, technology and talent to get ahead of disease together - so we can positively impact the health of billions of people and deliver stronger, more sustainable shareholder returns - as an organisation where people can thrive. Getting ahead means preventing disease as well as treating it, and we aim to positively impact the health of 2.5 billion people by the end of 2030.

Our success absolutely depends on our people. While getting ahead of disease together is about our ambition for patients and shareholders, it’s also about making GSK a place where people can thrive. We want GSK to be a workplace where everyone can feel a sense of belonging and thrive as set out in our Equal and Inclusive Treatment of Employees policy. We’re committed to being more proactive at all levels so that our workforce reflects the communities we work and hire in, and our GSK leadership reflects our GSK workforce.

GSK is an Equal Opportunity/Affirmative Action Employer. All qualified applicants will receive equal consideration for employment without regard to race, color, national origin, religion, sex, pregnancy, marital status, sexual orientation, gender identity/expression, age, disability, genetic information, military service, covered/protected veteran status or any other federal, state or local protected class.

**Important notice to Employment businesses/ Agencies**

Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure GSK’s compliance to all federal and state US Transparency requirements. For more information, please visit GSK’s Transparency Reporting For the Record site.

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