Director, Commercial Manufacturing
Sacramento, CA
Manufacturing - Production / Regular, Full-Time Employee / On-site
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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 Director, Commercial Manufacturing is responsible for leadership of cell therapy manufacturing operations and production support functions to ensure reliable, compliant, and timely delivery of patient-specific therapies. This role drives consistent batch execution, operational discipline, and cross-functional alignment to meet on-time patient delivery while maintaining the highest standards of quality and safety.
The Director will build and sustain robust production systems, embed lean manufacturing principles, and lead continuous improvement initiatives to scale operations in a dynamic, GMP-regulated environment.
Physical Demands
Production Associate Roles: 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.
Most roles 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), jewelry, or facial piercings is not permitted in the cleanroom, and any skin conditions that cause shedding must be disclosed.
Work Conditions
Many roles must be able to work at either Orca Bio Sacramento location (3400 Business Dr. or 7910 Metro Air Pkwy) based on operational needs, as well as regularly participate in video-based meetings. Also, may be required to work scheduled overtime, weekends, or holidays based on business needs.
Essential Duties & Key Responsibilities:
Commercial Manufacturing Oversight
Provide strategic and day-to-day leadership for GMP manufacturing operations
Ensure consistent execution of manufacturing batches in alignment with production schedules and patient needs
Drive right-first-time execution and minimize deviations, batch failures, and delays
Ensure rapid resolution of manufacturing issues with minimal impact to patients
Patient-Centric Delivery Execution
Own manufacturing performance metrics tied to patient delivery:
On-time batch release and shipment
Cycle time adherence
Schedule attainment
Partner cross-functionally with Quality, Supply Chain, and Patient Operations to ensure seamless delivery of autologous therapies
Quality and Compliance
Ensure full compliance with cGMP, regulatory requirements, and internal quality systems
Partner closely with Quality Assurance to:
Drive deviation reduction and investigation closure
Maintain inspection readiness
Support audits and regulatory inspections
Promote a strong quality culture and accountability at all levels
Safety Leadership
Champion a culture of safety across manufacturing operations
Ensure compliance with EHS requirements and proactively mitigate risks
Lead investigations and corrective actions for safety incidents
Lean Manufacturing and Continuous Improvement
Establish and sustain lean manufacturing systems, including:
Visual management
Standard work
Tiered accountability
Daily performance management
Lead continuous improvement initiatives to enhance:
Throughput
Capacity utilization
Cost efficiency
Process robustness
Utilize data-driven decision-making and performance dashboards
People Leadership and Development
Build, lead, and develop high-performing teams across manufacturing and support functions
Establish clear goals, performance expectations, and accountability structures
Foster a culture of engagement, ownership, and continuous learning
Minimum Qualifications:
Bachelor's degree in Life Sciences, Engineering, or related field (required)
10+ years of experience in biopharmaceutical manufacturing, with a strong preference for cell or gene therapy
5+ years in senior leadership roles managing GMP manufacturing teams
Proven experience in autologous or patient-specific manufacturing environments
Demonstrated success in scaling manufacturing operations and improving execution performance
Deep knowledge of cGMP regulations and regulatory expectations
Strong background in lean manufacturing and operational excellence methodologies
Preferred Qualifications:
Advanced degree (MS, MBA, or PhD) preferred
$175,000 - $210,000 a year
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. 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, PTO, 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.
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.
We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.
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