Technician, Quality Control, 3rd Shift

More than one million people in the United States today are fighting blood cancer. While a traditional allogeneic stem cell transplant has been the best hope for many, the transplant itself can prove fatal or lead to serious conditions, such as graft vs. host disease. Orca Bio is a late-stage biotechnology company redefining the transplant process by developing next-generation cell therapies with the goal of providing significantly better survival rates with dramatically fewer risks. With our purified, high-precision investigational cell therapies we hope to not only replace patients' blood and immune systems with healthy ones, but also restore their lives.

We have built a state-of-the-art, 100,000-square-foot manufacturing facility in Sacramento, CA (7910 Metro Air Pkwy) to ensure the consistent and reliable delivery of our high-precision cell therapy products. This site is essential to advancing our clinical pipeline and supporting future commercial availability of our life-saving therapies.

Summary of Role: The Technician, Quality Control (Analytical) conducts routine and non-routine testing to ensure the highest quality standards in our cell therapy manufacturing facility. Your work will play a crucial role in maintaining the integrity and safety of our cell therapy products.

This is a 3rd shift-based position, working on-site Monday through Thursday, from 10:00pm–8:30am, on a 4x10 schedule.

• Perform a range of basic to moderately complex analytical tests following cGMP guidelines
• Test routine and non-routine samples; document results with accuracy and compliance
• Maintain, calibrate, and troubleshoot lab equipment to ensure functionality
• Prepare reagents and aliquot samples, including aseptic techniques when needed
• Monitor and maintain inventory of lab supplies
• Support assay transfers, validations, and equipment qualifications
• Aliquot samples as required, including aseptic aliquoting
• Actively participate in group and project teamwork; project and process improvements
• Work cross-functionally with Manufacturing, QC, and QA to resolve issues and implement corrective actions
• Follow all cGMP documentation and procedural standards
• Perform additional duties as assigned to support the Quality team

• A.S. or B.S. in a relevant scientific discipline (biology, microbiology, etc.) required
• High attention to detail and a commitment to data integrity
• Strong organizational, communication, and problem-solving skills
• Ability to work both independently and collaboratively in a fast-paced, regulated setting
• Flexible and responsive to changing priorities and team needs
• Preferred: Experience with analytical assays (e.g., flow cytometry, ELISA, PCR)
• Preferred: Familiarity with aseptic technique in a GMP or biotech setting

The anticipated annual salary range for this job is based on prior experience in the role/industry, education, location, internal equity, and other job-related factors as permitted by law. For remote-based positions, this range may vary based on your local market. You will also be eligible to receive pre-IPO equity, in addition to competitive medical, dental, and vision benefits, flexible PTO, 401(k) plan, life and accidental death and disability coverage, and parental leave benefits. Other perks include free daily lunches and snacks at our on-site locations.

Who we are

We are driven by a passion for science and compassion for patients. We act with urgency to ensure our treatments are one day accessible to all who need them.

We live by our core values of passion, courage, and integrity. Excellence in our work means the chance to unlock a better quality of life for our patients, and with that comes tremendous responsibility.

We innovate on a path that hasn’t been paved. We embrace an entrepreneurial spirit and take calculated risks to achieve our mission. We aren’t afraid to ask “why not” and challenge the status quo.

We maintain a start-up culture of camaraderie and leadership by example, regardless of title.

We’re proud to be an equal opportunity employer, and recognize that celebrating our differences creates stronger, lasting solutions that better serve our team, our patients and their healthcare providers.

Notice to staffing firms

Orca Bio does not accept resumes from staffing agencies with which we do not have a written agreement and specific engagement for a particular opening. Our employment activities, inquiries and offers are managed through our HR/Talent team, and all candidates are presented through this channel only. We do not accept unsolicited resumes, and we rarely outsource recruitment.