Analytical Development Scientist - CGT

landmarkbio; Watertown (MA); Presencial; USD 85.000 - 125.000; Jornada completa

Descripción de la vacante

Artis BioSolutions is seeking an Associate Scientist to support Analytical Development and GMP Quality Control in a fast-paced CGT environment. You will execute specialized laboratory testing and contribute to development, qualification, and implementation of methods for clinical GMP release and product characterization.

This role offers mentorship and opportunities to lead analytical tasks across teams. The ideal candidate has a relevant degree with 5+ years in cGMP biotech, hands-on UHPLC or

Formación

• Bachelor's degree with 5+ years experience or Master's with 3+ years in cGMP biotech.
• Hands-on UHPLC or PCR instrumentation in regulated environments.
• Molecular biology, biophysical characterization, or CGT techniques.
• Detail-oriented with strong problem-solving and communication.
• US work authorization; immediate start.

Responsabilidades

• Develop, optimize, and troubleshoot analytical methods for CGT safety and quality.
• Execute routine and advanced testing in a cGMP manufacturing setting.
• Support method transfer from development to Quality Control and manufacturing.
• Draft protocols, reports, and GMP-compliant documentation.
• Collaborate with QA, Manufacturing, and Development to meet standards.

Conocimientos

Detail-oriented

Troubleshooting

Communication skills

Leadership & collaboration

Educación

Bachelor's degree in a relevant field

Master's degree in a related field

Herramientas

UHPLC platforms

PCR platforms

Descripción del empleo

Artis BioSolutions is seeking an Associate Scientist to support Analytical Development and GMP Quality Control in a fast-paced CGT environment. You will execute specialized laboratory testing and contribute to development, qualification, and implementation of methods for clinical GMP release and product characterization.

This role offers mentorship and opportunities to lead analytical tasks across teams. The ideal candidate has a relevant degree with 5+ years in cGMP biotech, hands-on UHPLC or