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Supervisor, Quality Control

Job in Sacramento, Sacramento County, California, 95828, USA
Listing for: Orca Bio
Full Time position
Listed on 2026-03-11
Job specializations:
  • Quality Assurance - QA/QC
  • Healthcare
Salary/Wage Range or Industry Benchmark: 70000 - 110000 USD Yearly USD 70000.00 110000.00 YEAR
Job Description & How to Apply Below

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.

The Supervisor, Quality Control (QC) is responsible for overseeing daily operations within the QC laboratory to ensure compliance with regulatory standards, internal procedures, and quality expectations. This position plays a critical role in maintaining data integrity through audit trail reviews, leading investigations of out‑of‑specification (OOS) results and deviations, and ensuring the lab remains in a consistent state of inspection readiness.

We are multiple positions across the following schedules:

Day

Shift:
  • 6am to 7pm
  • 6:30am to 7:30pm
Night

Shift:
  • 6:00pm to 6:30am
  • 6:30pm to 7:00am
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 colour vision to safely perform critical tasks such as visual inspection of materials, equipment, and labeling, including distinguishing colour‑coded components 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 (makeup, painted nails), jewellery, 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.
Essential Duties &

Key Responsibilities:
  • Lab work and supervisor roles:
    Lead routine quality control testing on raw materials, process intermediates, and final cell therapy products. Supervise the QC team, supporting data verification, leading investigations, prioritising tasks, and collaborating with other teams. Perform tests, ensure compliance, maintain the lab, prepare reagents, aliquot samples, assist with assay transfer/validation, train staff, and manage supplies.
  • Data Integrity and Audit Trail Review:
    Ensure GMP compliance by conducting audit trail reviews, identifying data integrity issues, and ensuring proper documentation. Lead and document QC testing results, and assist with preparing and reviewing batch records, SOPs, and related documentation to ensure adherence to cGMP regulations.
  • Investigations and CAPA:
    Oversee Quality System investigations into OOS results, atypical findings, and lab deviations. Ensure root cause analysis, documentation, and implementation of CAPAs, collaborating with cross‑functional teams to resolve quality issues.
  • Lab Inspection Readiness:
    Monitor lab conditions to ensure compliance with cGMP and FDA/EMA regulations, maintaining documentation, equipment logs, and records for inspection readiness. Lead preparation activities for internal and external audits, including document reviews and mock audits.
  • Team Leadership and Oversight:
    Manage and support a team of QC analysts, overseeing scheduling, training, and performance evaluations. Provide technical guidance and mentorship to ensure…
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