Senti Bio seeks a highly motivated and experienced individual with a background in Analytical Development of flow-cytometry (FACS) based methods. The successful candidate will contribute to the advancement of Sentis proprietary immunotherapeutic cell engineering platforms into the clinic. The role will drive the development of FACS-based methods for characterization and release of Sentis drug products. Specifically this role will support the development of new and existing methods assess qualification readiness and transfer of methods to QC and use FACS and other methods to support characterization of our drug products and manufacturing processes. The ideal candidate is technically strong in the development and troubleshooting of FACS-based methods with a desire to educate others on best practices an enthusiastic team-player able to think outside of the box to achieve goals and interested in expanding their Analytical Development experience.
Responsibilities
Collaborate with R&D to understand relevant product characteristics.
Identify and develop key FACS methods for characterization and release of drug product and manufacturing processes.
Testing support to enable product and process understanding.
Drive the development qualification readiness and transfer of release methods to QC
Collaborate with Analytical team members in the development of other assays as needed such as immune- or cell-based functional assays.
Support the writing of CMC sections of Regulatory filings.
Write Test Methods and SOPs.
Independently perform experiments analyze data and present results.
Successfully design execute and document laboratory procedures and experiments with great attention to detail.
Qualifications
Graduate degree in Cell Biology or related life science field. PhD with 2 years or Masters with 4-6 years of hands-on industry experience in Analytical Development Quality or some combination of the above required experiences
Industry or academic experience with CAR-T CAR-NK cell therapy or immunology is a plus.
Demonstrated experience with cGMP workflows from development to pre-qualification qualification validation and tech transfer to QC
Significant hands-on experience with developing multi-color (5) flow cytometry-based assays
Experience with Regulatory filings
Ability to multitask and meet deadlines in a fast-paced environment
Ability to think critically and demonstrate troubleshooting and problem-solving skills with team members and third-party vendors.
Must be a team player proactive and willing to work in a small team environment
Must have excellent verbal and written communication skills including experience delivering presentations to executive stakeholders and external partners
Proficient with MS office and other commonly used software and technology platforms
Self-motivated and eager to take on temporary responsibilities outside of initial job description
Salary and Benefits
Compensation for this role includes hourly base pay.
The hourly base pay for this role is $64.00- $79.00. Starting pay is determined by multiple job-related factors including a candidates skills education and experience level benchmark and internal parity.
Significant growth opportunity as the company expands.
Empathetic supportive and collaborative colleagues and work environments
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