GlaxoSmithKline
Job Description
Are you interested in joining a Molecular Analytics group within the Analytical R&D department in the US? We are looking for a highly motivated Associate Scientist for this impactful role. The position of
Scientist Molecular Analytics
could be an ideal opportunity for you. As an
Associate Scientist Molecular Analytics , you will collaborate with high-performing CMC scientists on industry-disruptive technology platforms. Your primary responsibilities will include designing and developing analytical methods using Quality by Design (QbD) principles to support drug substance and drug product characterization, product and process development, and the development and transfer of release methods for GMP testing across the US Technical R&D portfolio. You will also be involved in implementing NGS technology to enhance CMC platforms and may serve as a Subject Matter Expert in NGS data analysis. The role involves working in a highly collaborative environment with approximately 70-80% of your time spent in the lab. This role offers the opportunity to lead key activities that will advance your career. Your responsibilities will include: Developing, optimizing, and qualifying methods for safety and quality assessments of vaccine candidates. Collaborating with Analytical Department teams to determine quality control strategies and support method validation and impact assessments. Streamlining workflows related to method development, qualification, training, transfer, and comparability. Serving as a subject matter expert for molecular methods and providing regulatory support. Supporting new technology assessment and licensing activities. Prioritizing deliverables from multiple programs with competing interests. Why you?
Basic Qualifications:
We are seeking professionals with these required skills: Master's Degree with 2-5 years of industry experience in biology, biochemistry, or pharmaceutical sciences. Experience with nucleic acid analysis and molecular biology and biochemistry techniques in wet lab settings. Preferred Qualifications:
Additional desirable characteristics include: Experience with gene therapies, mRNA vaccines or therapeutics. Experience with analytical assay development, GMP testing, and regulatory compliance. Knowledge of molecular testing and diagnostics, including PCR, real-time PCR, digital PCR, DNA/RNA isolation, DNA cloning, and molecular probe techniques. Research experience in RNA biology. Experience with nucleic acid formulation and bioprocess development. Why GSK?
Our core values—Patient focus, Transparency, Respect, Integrity, Courage, Accountability, Development, and Teamwork—are central to our culture. The successful candidate will demonstrate capabilities such as: Operating at pace with agile decision-making, balancing evidence, judgment, and risk. Delivering high-quality results and overcoming challenges. Continuous learning and skill-building. Sustaining energy, building relationships, and fostering collaboration. Being budget-conscious and cost-effective.
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Are you interested in joining a Molecular Analytics group within the Analytical R&D department in the US? We are looking for a highly motivated Associate Scientist for this impactful role. The position of
Scientist Molecular Analytics
could be an ideal opportunity for you. As an
Associate Scientist Molecular Analytics , you will collaborate with high-performing CMC scientists on industry-disruptive technology platforms. Your primary responsibilities will include designing and developing analytical methods using Quality by Design (QbD) principles to support drug substance and drug product characterization, product and process development, and the development and transfer of release methods for GMP testing across the US Technical R&D portfolio. You will also be involved in implementing NGS technology to enhance CMC platforms and may serve as a Subject Matter Expert in NGS data analysis. The role involves working in a highly collaborative environment with approximately 70-80% of your time spent in the lab. This role offers the opportunity to lead key activities that will advance your career. Your responsibilities will include: Developing, optimizing, and qualifying methods for safety and quality assessments of vaccine candidates. Collaborating with Analytical Department teams to determine quality control strategies and support method validation and impact assessments. Streamlining workflows related to method development, qualification, training, transfer, and comparability. Serving as a subject matter expert for molecular methods and providing regulatory support. Supporting new technology assessment and licensing activities. Prioritizing deliverables from multiple programs with competing interests. Why you?
Basic Qualifications:
We are seeking professionals with these required skills: Master's Degree with 2-5 years of industry experience in biology, biochemistry, or pharmaceutical sciences. Experience with nucleic acid analysis and molecular biology and biochemistry techniques in wet lab settings. Preferred Qualifications:
Additional desirable characteristics include: Experience with gene therapies, mRNA vaccines or therapeutics. Experience with analytical assay development, GMP testing, and regulatory compliance. Knowledge of molecular testing and diagnostics, including PCR, real-time PCR, digital PCR, DNA/RNA isolation, DNA cloning, and molecular probe techniques. Research experience in RNA biology. Experience with nucleic acid formulation and bioprocess development. Why GSK?
Our core values—Patient focus, Transparency, Respect, Integrity, Courage, Accountability, Development, and Teamwork—are central to our culture. The successful candidate will demonstrate capabilities such as: Operating at pace with agile decision-making, balancing evidence, judgment, and risk. Delivering high-quality results and overcoming challenges. Continuous learning and skill-building. Sustaining energy, building relationships, and fostering collaboration. Being budget-conscious and cost-effective.
#J-18808-Ljbffr