Junior Scientist Product Development
il y a 1 semaine
Quantoom Biosciences, a Univercells company, is a technology innovator focused on mRNA from to solve some of the biggest challenges facing mRNA-based vaccines and therapeutics. We are committed to lower the entry barriers to making mRNA-based medicine from development up to mass production.
Based in Nívelles (Belgium), you will join an interdisciplinary team of passionate scientists, engineers, clinicians and business profiles developing an innovative end-to-end RNA production platform aimed at supporting (bio)pharma companies in all parts of the World with their mRNA-based pipeline.
At
Quantoom and
Univercells, our mission is to make health equally accessible to all.
This job is the perfect opportunity to contribute to our mission to achieve our mission:
biologics available and affordable to all
Responsibilities:
As a member of the Drug Delivery and Administration Research team within Quantoom's Research department, the Junior Scientist will work on the design, development, testing and/or optimization of the next-generation RNA manufacturing system.
In particular, the Junior Scientist:
- Contributes to the design, early development and testing of the nextgeneration RNA manufacturing system;
- Contributes to tactical planning of related projects, under supervision of the responsible Scientist;
- Contributes to the experimental design of proofofconcept, screening and optimization studies, under supervision of the responsible Scientist;
- Prepares experimental documentation (experimental protocol, data capture forms, study report);
- Performs or supervises laboratory experiments and ensures compliance with good scientific practices;
- Maintains process description and process history files throughout the innovation project;
- May provide scientific expertise pertaining to mRNA formulation and administration technology development at internal and external meetings;
- Supports (hands on) the engineering team and external partners in the design and development of new manufacturing technologies and systems pertaining to DP operations;
- Collaborates with external service providers and development partners on manufacturing projects (including project coordination, remote or inperson supervision of external workstreams, preparation or review of study documents etc.);
- Monitors emerging manufacturing technologies and scientific advancements in the field of mRNA drug product technologies.
Profil:
- Master's degree in bioengineering, (bio)chemical engineering, pharmacy or any life sciences degree offering academic knowledge of both biomolecular science, material sciences and chemical engineering (unit operations)
- An advanced degree in the field of drug delivery or administration technology development (e.g. PhD) or prior professional experience in the field is a considerable asset;
- Experience with microfluidic devices and/or pharmaceutical unit operations is a considerable asset;
- Experience with scientific protocols and laboratory equipment used in the field of drug product development, such as: mammalian cell culture and transfection, molecular biology techniques, relevant analytical technologies (e.g. DLS, spectrophotometry / fluorimetry / bioluminescence),
- Prior experience with nucleic acid formulation and/or administration technologies is a significant plus;
- Critical and independent thinker; analytical mindset;
- Innovative mindset / scientific creativity: natural inclination to challenge the status quo and ability to conceptualize feasible process improvements (both evolutions and revolutions);
- Ability to work with mínimal supervision;
- Ability to function in a highpaced, dynamic environment;
- Excellent writing and communication skills;
- Excellent organizational skills; ability to manage evolving priorities and objectives;
- Leadership skills; ability to influence without managerial authority;
- Ability to work in a crossfunctional and multicultural team;
- Fluent in English (written and spoken); knowledge of French is an asset.
Offer:
We offer a
VIE contract type for a duration between 12 and 24 months. Be sure you are eligible to a
VIE contract before applying. All specificity on
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