Technician, Quality Control - Day Shift
Orca Bio · Sacramento, CA
Apply on employer's site →- Category
- Quality Control
- Location
- California, US
- Posted
- May 28, 2026
- Salary
- $59,514–$64,474 / year (as published by the employer)
- Employer type
- Biotech
- Last checked
- Oct 17, 2026
The Technician, Quality Control - Day Shift 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. Day Shift Hours Worked: • 6:00am to 6:30pm or • 6:30am to 7:00pm Work Week Schedule: • Sunday, Monday, Tuesday + every other Wednesday or • Thursday, Friday, Saturday + every other Wednesday
Physical Demands
- Production Associates: 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, equipment, and labeling, including distinguishing color-coded components in a GMP environment.
- Must meet cleanroom gowning requirements, including wearing full gowning (face coverings, gloves, hoods, goggles) for up to 3 consecutive hours at a time, minimal movement in the cleanroom, and working with or around human blood, blood-derived materials, cells, other biological materials, and alcohol-based sprays. Use of cosmetics (makeup, painted nails), jewelry, or facial piercings is not permitted in the cleanroom, and any skin conditions that cause shedding must be disclosed.
- Must be comfortable regularly participating in video-based meetings.
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
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