Scientist, Analytical Development
2 months ago
At Turnstone, the science drives decision-making and our therapeutics are designed with the patient foremost in mind. We continue to build a world-class, high-performing company that embraces being a learning organization with a sense of urgency. Imagine coming to work every day where over-communication, transparency, teaching, listening, asking, thinking, working hard, and having fun are normal - actually, expected? Imagine having a coach, mentor, peers, and partners where candid feedback, self-improvement, risk taking, failing, learning from that failing, and succeeding thereafter are what we call ‘another day at Turnstone’? If you are a passionate person, and our science excites you - this opportunity may be for you.
**POSTITION OVERVIEW**
**KEY RESPONSIBILITIES**
- Contribute to the development, optimization, qualification, and transfer of analytical assays, including potency and phenotypic profiling for both lot release and characterization of cell therapy products.
- Design and execute assays and characterization studies to interrogate immune cell biology and function with mínimal assistance.
- Plan, coordinate, and execute analytical testing using multi-parametric flow cytometry, ELISA/Ella/MSD, and molecular methods.
- Collaborate cross-functionally and support routine Process Development (PD) sample testing and other internal/external studies supporting regulatory submission.
- Document laboratory procedures and experiments with great attention to detail, including Electronic Lab Notebook (ELN) record keeping.
- Support method transfer to partners at external contract manufacturing organizations, including compilation of documentation (protocols, test methods, reports).
- Develop, revise, approve, and own SOPs (Standard Operating Procedures) and technical (transfer, validation, bridging, etc.) protocols / reports.
- Analyze data, prepare reports and data packages for communicating with key stakeholders, senior management, and external partners.
- Willingness to travel to external partner locations for method‑related support, when necessary.
- Additional duties as assigned.
**QUALIFICATIONS**
- MS with 4+ years OR PhD in Biology with 1+ years of Analytical Development experience.
- Hands-on experience with flow cytometry and ELISA-based assay development optimization, and troubleshooting is required.
- Experience with cell-based potency assessment and functional characterization of drug products is desired.
- Strong technical acumen, with a keen eye for detail in data analysis and record-keeping skills.
- Basic understanding of ICH guidelines for assay qualification/validation.
- Experience with data analysis such as GraphPad Prism, FlowJo and JMP.
- Comfortable in a fast-paced environment with mínimal direction and able to adjust workload based upon changing priorities.
- Self-motivated, detail-oriented, and willing to accept temporary responsibilities outside of initial job description.
- Demonstrated ability to manage multiple tasks/projects with demanding timelines.
- Strong interpersonal, teamwork, and organizational skills; effective oral and written communication skills.
- Occasional travel to support cross-functional workshops or strategy/planning activities.
**COMPENSATION / BENEFITS**
At Turnstone, we prioritize the well-being and success of our team. Join us and enjoy a competitive compensation package, including a base salary and performance-based bonuses. Our comprehensive benefits include:
- **
Healthcare Coverage**: Medical, dental, and vision insurance for you and your dependents.
- ** Retirement Planning**: 401(k) plan with employer contributions.
- ** Time Off**: Generous paid time off, including vacation, sick leave, and holidays.
- ** Workplace Flexibility**: Flexible schedules and remote work options.
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