External QC Principal Research Associate at Sana Biotechnology

South San Francisco, California, United States -

Full Time

Start Date

Immediate

Expiry Date

19 Jan, 26

Salary

140000.0

Posted On

21 Oct, 25

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Cell Biology, Immunology, Flow Cytometry, GMP Implementation, SOP Authoring, Quality Systems, Data Analysis, Method Development, Technical Support, Change Controls, Investigations, CAPAs, Statistical Software, Analytical Methods, Troubleshooting, Documentation

Industry

Biotechnology Research

Description

About the role Sana Biotechnology is growing, and we are hiring new team members who believe in the potential of engineered cells as medicines, who are passionate about delivering the possible to patients, and who lead with the desire to work on novel ideas. As a Principal Research Associate, Analytical Development, you will report to the Senior Director, Analytical Development and Quality Control. You will support a wide variety of test methods for Sana’s cell therapy products while working with a cross-functional team on method development, transfer, and qualification, providing onsite training and technical support at CDMOs, and overseeing contract test labs. This role is onsite in South San Francisco, CA. What you’ll do Collaborate with the Analytical Transfer Lead to transfer release methods to contract development and manufacturing organization (CDMO) and provide onsite training and technical support to enable GMP implementation Assist with the coordination of QC activities at CDMO and contract test labs, including providing technical guidance on troubleshooting and participating in data review Perform routine release, characterization, and stability testing using flow cytometry methods as needed Document testing according to Good Documentation Practices and GMP data integrity requirements Work with method developers and external partners to design and execute studies supporting method development, transfer, and qualification Work cross-functionally with Process Development, Quality Assurance, and other departments to optimize analytical testing, product specifications, and process control strategies Author and approve method qualification protocols and reports as needed Own or contribute to change controls, investigations, and CAPAs Author specifications, test methods, sampling plans, certificates of analysis, and stability reports Assist in developing quality systems, establishing SOPs, work instructions, and other procedures to support QC operations Manage laboratory equipment through installation, qualification, maintenance, and retirement What we’re looking for S. or M.S. in Cell Biology, Immunology, or a related scientific discipline with 5-6 years related work experience Experience performing multi-color flow cytometry methods and data analysis Experience transferring methods to CDMOs or contract test labs and GMP implementation Experience authoring and/or reviewing SOPs, test methods, and other quality-related documents Strong knowledge of GMP requirements and regulations Strong knowledge of GMP testing and quality systems Experience with change controls, deviations, and CAPAs Ability to work in a dynamic environment to deliver on-time project completion with tight timelines What will separate you from the crowd Experience with a variety of analytical methods, including flow cytometry, ddPCR, and cell-based assays Experience in flow cytometry, ddPCR, and cell-based assay development and qualification Experience using statistical software just as JMP Experience implementing rapid safety test methods (e.g. BACT/ALERT) in place of conventional methods What you should know Travel to CDMO to provide onsite training and technical support is required There may be potential exposure to BSL2 and BSL2+ biohazard materials Occasional off-hours or weekend work may be required Physical Demands: Employees in this position may be required to perform the following physical activities: standing, walking, and sitting for extended periods of time; frequent use of the hands, fingers, wrist, and greater arm to handle small materials, tools, boxes, and trays; lifting and carrying objects up to 10 Ibs; occasional overhead reaches and lifts; occasional lifts and reaches below the knee; occasional pushing and pulling of materials and objects with moderate forces; occasional crouching/kneeling, twisting, and squatting movements. Must be able to successfully pass all job-related tests and certifications required for working in a cGMP, quality environment including but not limited to: inspections and GMP requirements to perform essential functions of the job. The base pay range for this position at commencement of employment is expected to be between $115,000-$140,000 annually; however, base pay offered may vary depending on multiple individualized factors, including market location, job-related knowledge, skills, and experience How we work together for patients Lead from every seat – we seek to understand, act with honesty, and engage in the crucial conversations Thrive as a team – we hire amazing people, are intensely curious, and cultivate inclusion and personal connectivity Make it happen – we value vigorous debate, alignment around our decisions, and resilient execution Get to know us At Sana, we believe that a diverse workforce strengthens us as a company and helps us to achieve our mission to meaningfully change the outcome of many human diseases. This belief is a pillar of our business and is critical to our success. Our goal is that Sana is the place for talented people to bring their authentic selves to work, to have a great career and to deeply, positively impact patients. Core to our values, we believe there is nothing more important than the health and wellness of you and your family. For benefit eligible employees, we cover 100% of the cost for employee health coverage and offer generous time-off (various paid time off benefits, such as holidays, vacation, sick time, and parental leave), short- and long-term disability, employer paid basic life insurance, additional voluntary life insurance protection, financial wellness programs including financial planning resources, a 401(k) Plan with an immediately vested employer match, Tuition Reimbursement and Student Loan Repayment, Employee Stock Purchase Plan, commuter subsidy and a variety of wellness offerings to support each person individually. For more details on our benefits, visit Sana’s Benefits Portal. We are committed to providing a workplace free of discrimination and harassment based on race, color, religion, age, gender, national origin, ancestry, physical or mental or sensory disability (including the use of a trained guide dog or service animal by a person with a disability), genetic information, actual or perceived HIV or Hepatitis C infection, medical condition (cancer or a record or history of cancer and genetic characteristics), marital status, sexual orientation, sexual preference, pregnancy (including childbirth and related medical conditions), disability, veteran status, political ideology, social class (including caste/caste identity), taking or requesting statutorily protected leave, status as a victim of domestic violence, sexual assault or stalking, or any other basis prohibited by applicable law. To perform this job successfully, you must be able to perform each job responsibility satisfactorily. The job description listed above is representative of the knowledge, skills, and/or abilities required for this position. Reasonable accommodations may be made to enable individuals with disabilities to perform the functions described above.

Responsibilities

The Principal Research Associate will support a variety of test methods for cell therapy products, collaborating with cross-functional teams on method development and qualification. This role includes providing onsite training and technical support at CDMOs and overseeing contract test labs.