Site Name: USA - Maryland - Rockville Posted Date: Apr 22 2022 Are you energized by the challenge of shaping and accelerating the scientific expertise of several vaccine programs, including mRNA-based vaccines? If so, this Scientist position within the Molecular Analytics platform of the Analytical R&D Department is for you and could be an exciting opportunity to consider. Job Purpose As Scientist within the Molecular Analytics platform, you will be in charge of implementing, designing and developing methods for the detection and quantification of nucleic acids based on up-to-date nucleic acid technologies (NAT) and, in particular, methods aiming at characterizing plasmids (topology, conformation, sequence, quantity, etc.), mRNA Drug Substances (content, integrity, identity) and mRNA-LNP Drug products (monovalent and multivalent), used for production of mRNA vaccines. The use of direct nucleic acid quantification methods (e.g. CRISPR-based assays, digital counting through optical barcodes, branched DNA assays, etc.) will part of the activities of the hired Scientist. You will join the the Analytical Development Department, where the Molecular Analytics Platform is in charge of developing modern, state-of-the-art molecular methods to analyze (i.e. detect, identify, quantify and characterize) nucleic acids at all stages of vaccines development. You will be in charge of the design and development of NAT-based analytical methods to support product and process development, to develop and transfer release methods for GMP testing for Phase 1, Phase 2 and Phase 3, according to Quality by Design principles and in partnership with Technical Research and Development functions, Quality and Regulatory. Your responsibilities: Work on the bench in the labs (> 70%) Interact with Belgium- and US-based team members Contribute to the development, qualification, validation and transfer of innovative genetic characterization assays/technologies based on state-of-the-art NAT Ensure the development of analytical methods for purity, identity and sterility Execute analytical methods for the genetic characterization of genetically engineered microorganisms, including recombinant plasmids Interact and act in a complex matrix with several stakeholders from different departments (Research, Development, QC, RA, QA) Interact with other GSK Vaccines R&D Centers (in US and IT) and external CMOs Ensure implementation of QbD (Quality by design) in the development of assays Agile principles driven Develop detailed experimentation protocols and executes the planning/organization of the experiments in his/her scope of activities Analysis and interpretation of the data, including reporting and presentation Contribute to the various activities of the group Why you? Basic Qualifications: We are looking for professionals with these required skills to achieve our goals: Master degree (biotechnology, molecular biology, biochemistry, (molecular) bacteriology, (molecular) microbiology, …) with 3 to 5 years of experience in the industry (in biologics / biopharmaceuticals / pharmaceutics) or equivalent by experience Experience in a lab environment focusing on analytics of biomolecules Diversified expertise in molecular biology (diversity of techniques and technologies as well as diversity of subjects) Ability to conduct literature and online research, continuous search of new methods Nucleic acid extraction Experience in PCR, QPCR and ddPCR Direct nucleic acid quantification methods (e.g. CRISPR-based assays, digital counting through optical barcodes, branched DNA assays, etc.) Preferred Qualifications: If you have the following characteristics, it would be a plus: Bacteriology, microbiology techniques, including plasmid biology Sanger and high throughput sequencing technologies Design of primers and probes using recognized softwares, design of LNA-containing primers and probes, design probes for multiplex assays, design of taqman probes. Molecular Biology techniques (including Southern blot, restrictions, reverse transcription, in vitro transcription, electrophoresis, etc.) Identification of critical method parameters and plan to evaluate them Team work Good writing skills Good communicator Attention for details, eager to learn and driven by curiosity Why GSK? At GSK, we have already delivered unprecedented change over the past four years, improving R&D, becoming a leader in Consumer Health, strengthening our leadership, and transforming our commercial execution. Now, we're making the biggest changes we've made to our business in over 20 years. We're on track to separate and create two new companies in 2022: New GSK with a leading portfolio of vaccines and specialty medicines as well as R&D based on immune system and genetics science; and a new world-leading consumer healthcare company of loved and trusted brands. With new ambition comes new purpose. For New GSK, this is to unite science, talent and technology to get ahead of disease together - all with the clear ambition of delivering human health impact; stronger and more sustainable shareholder returns; and as a new GSK where outstanding people thrive. Getting ahead means preventing disease as well as treating it. How we do all this is through our people and our culture. A culture that is ambitious for patients - so we deliver what matters better and faster; accountable for impact - with clear ownership of goals and support to succeed; and where we do the right thing. So, if you're ready to improve the lives of billions, join us at this exciting moment in our journey. Join our challenge to get Ahead Together. *LI-GSK #LI-GSK If you require an accommodation or other assistance to apply for a job at GSK, please contact the GSK Service Centre at 1-877-694-7547 (US Toll Free) or +1 801 567 5155 (outside US). 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