Scientist Jobs

About The Position

Requirements

• At least 3 years of relevant experience with an MS degree in Chemistry, Biology or a related scientific field; or at least 5 years of relevant experience with a BA or BS degree in Chemistry, Biology or a related scientific field.

Nice To Haves

• At least 2 years of hands-on experience with analytical techniques such as qPCR, ddPCR, ELISA, microbiology and cell-based assays.
• In-depth knowledge of ELISA or PCR method development, instruments, method controls and reagent inventory management systems.
• Proficiency with aseptic technique and general laboratory assays, such as cell culture, flow cytometry and molecular biology.
• Understanding of patient material, product and process characterization.
• Demonstrated ability to develop methods, techniques and evaluation criteria, and to interpret experimental results.
• Strong critical thinking, troubleshooting and problem-solving skills with close attention to detail.
• Proficiency with Microsoft Word, Excel and PowerPoint, Smartsheet, Prism, JMP and other data analysis applications.
• Highly collaborative, with excellent interpersonal, verbal and written communication skills.
• Self-motivated and comfortable working with minimal direction in a fast-paced environment, adjusting to changing priorities.

Responsibilities

• Design and execute non-routine ELISA and/or PCR experiments to support process development and product characterization.
• Develop, qualify, execute and document PCR methods to study and characterize processes used to produce T cell therapies.
• Select appropriate methods and techniques, and develop and refine analytical methods and experimental approaches.
• Troubleshoot analytical methods and instruments; recommend alternatives and research new methods and techniques.
• Analyze and interpret data using advanced analysis software; draw and defend scientific conclusions.
• Support transfer of ELISA and/or PCR assays from method developers to the analytical testing group.
• Perform reagent titration and lot-checking/verification, and maintain the proficiency testing database.
• Review notebooks and verify data to uphold ALCOA+ principles and data integrity.
• Author, review and edit technical documents, including validation protocols and reports and analytical development reports.
• Lead improvement projects, such as Operational Excellence initiatives, within the team.
• Provide user training on instruments and sample analysis, and mentor and cross-train analysts on analytical methods.
• Present results and conclusions in group meetings and communicate effectively with cross-functional partners.

Benefits

• Paid time off.
• Company-sponsored medical, dental, vision and life insurance plans.
• May be eligible for a discretionary annual bonus.
• May be eligible for discretionary stock-based long-term incentives; eligibility may vary by role.