Technician, Quality Control - Night Shift

Technician, Quality Control – Night 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 versus 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. 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. Night Shift Hours Worked 6:00 pm to 6:30 am 6:30 pm to 7:00 am Work Week Schedule Sunday, Monday, Tuesday + every other Wednesday Thursday, Friday, Saturday + every other Wednesday Physical Demands Must have visual acuity of 20/20 (corrected or uncorrected) and normal color vision to safely perform critical tasks such as visual inspection of materials and labeling in a GMP environment. Must be able to meet cleanroom gowning requirements, including wearing full gowning (face coverings, gloves, hoods, goggles) for extended periods, as needed. Use of cosmetics, painted nails, jewelry, or facial piercings is not permitted in the cleanroom, and any skin conditions that cause shedding must be disclosed. Work Conditions Must be able to work at either Orca Bio Sacramento location (3400 Business Dr. or 7910 Metro Air Pkwy) based on operational needs. Must be comfortable regularly participating in video‑based meetings. May be required to work scheduled overtime, weekends, or holidays based on business needs. Job Duties & Key Responsibilities 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. Minimum Qualifications 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 position 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. Full‑time employment positions will also be eligible to receive pre‑IPO equity and annual bonus, in addition to competitive medical, dental, and vision benefits, paid time off, 401(k) plan, life and accidental death and disability coverage, and parental leave benefits. Other perks include subsidized daily lunches and snacks at our on‑site locations. #J-18808-Ljbffr