About this role
Primary Responsibilities
- Understands and interprets research protocols and procedures
- Communicates questions, observations, and/or data findings with scientists to resolve challenges and gain scientific understanding
- Independently performs routine testing methodologies for AAV gene therapy vectors – including assays PCR-based assays and/or ELISA
- Identifies risks in assay performance, communicates them effectively, and supports mitigation efforts
- Maintains cell cultures and ensures reagents/supplies are ready-to-use
- Collaborates across teams to raise awareness and/or to collect, analyze, document and report data
- Performs routine laboratory activities such as material procurement, media and reagent preparation, and inventory organization
- Participates in regular team meetings (both in-person and virtually)
Required Skills and Qualifications
- BS in Chemistry, Biochemistry, Life Sciences, Pharmaceutical Sciences, Chemical Engineering, or a related field with 1 – 3 years of relevant, hands-on experience in academia and/or industry
- Hands-on experience with gene therapy products is highly desirable
- Working knowledge of analytical assay development, including molecular, immuno-, and cell-based assays (e.g., dPCR/ddPCR/qPCR, ELISA)
- Basic understanding of FDA regulations, cGxPs, and ICH guidelines is a plus
- Proficiency in using electronic laboratory notebooks (e.g., Benchling) for documentation, data analysis, and collaboration
- Strong organizational and problem-solving skills, with the ability to manage multiple tasks in a fast-paced environment
- A proactive, team-oriented attitude and excellent communication skills.