Job description

About Ossium Ossium’s mission is to improve the health, vitality, and longevity of human beings through bioengineering. We develop, manufacture, and bank cell therapy products that apply the power of stem cell science to revolutionize treatment for patients with blood, immune, and orthopedic diseases. At Ossium, we empower our employees, maintain the highest standards of operational excellence, and are a force for good. About the Job The Operations Manager, HPC leads the hematopoietic progenitor cell (HPC) production team that turns organ donor vertebral bodies into bone marrow and other cell therapy products. You will own the HPC value stream at our Indianapolis facility, from donor intake and allocation to cell processing and cryopreservation, and the supervisors and operators who run it across shifts. You will also lead the cross-functional Core Team that ensures reliable production of HPC, Marrow and work closely with Tissue Production, MSAT, Engineering, Quality, and Supply Chain. This is a hands-on leadership role in a cleanroom environment: you will spend real time on the floor, and you will also own the metrics, the investigations, and the plan for scaling the team. Required Qualifications BS/BA in a technical field or equivalent experience 5+ years of manufacturing or related experience 3+ years in a formal people-leadership role Working knowledge of aseptic technique, cleanroom operations, and cGTP/cGMP requirements Experience owning deviations, investigations, and CAPAs, including root cause analysis Excellent written and oral communication skills, with the ability to present results to cross-functional stakeholders High level of attention to detail and the ability to operate with organization and urgency in a dynamic environment Preferred Qualifications Advanced degree in a relevant scientific discipline Direct experience managing teams in an aseptic manufacturing environment Trained in statistical process control and continuous improvement tools and methodologies Experience supporting FDA or other regulatory and accreditation inspections Experience with process validation and technology transfer from development into routine production Familiarity with lean or tiered daily management practices Key Responsibilities Own daily HPC production output from donor intake through cryopreservation and initial inventory, ensuring every gift is used for its authorized purpose Manage HPC Production Supervisors across shifts, ensuring processes are scheduled with appropriately trained and qualified personnel Serve as operator, verifier, or trainer during clinical production as needed Develop and report production metrics such as throughput, yield, right-first-time documentation, deviation rate, and cycle time, and drive action where targets are missed Perform technical review of production batch records and ensure traceability of donor products through final disposition Write and oversee event reports, investigations, risk assessments, and CAPAs, including effectiveness checks Lead operational changes through project management, document creation, batch record revision, and risk assessment Serve as hiring manager for HPC production roles and oversee onboarding, qualification, and ongoing training for the team Serve as Core Team Leader for HPC, Marrow: own the Core Team charter, lead the daily meeting, set the agenda for weekly meetings, and drive cross-functional alignment across Production, Quality, Engineering, and MSAT Accountable for the Core Team balanced scorecard covering safety, quality, process control and capability, variability reduction, throughput, supply chain planning, productivity, training, and equipment reliability Keep the HPC process in control, capable, and compliant, prioritizing effectiveness before efficiency, and lead periodic formal process reviews and Annual Product Review feedback Establish the Core Team floor presence schedule and ensure development plans are in place for frontline supervisors and staff Partner with Tissue Production, MSAT, Engineering, Quality, Supply Chain, and Facilities on shared suites, materials, equipment, and process improvements Physical Requirements Must be able to work in a moderately noisy environment Must be able to work around biohazardous materials and chemicals Required to work the majority of the shift aseptically in a controlled environment with limited breaks. This environment requires special gowning (ie. over the head, face, hands, feet and body). Must be able to lift, push, pull and/or carry up to 50 lbs Must have sufficient manual dexterity, hand/finger coordination, wrist mobility, wrist stability, and grip strength to handle, feel, grasp, manipulate, and operate objects, manual and power tools, equipment, and controls safely and accurately. Regularly required to sit, stand, walk, squat, balance, climb, stoop, kneel, crouch and reach with arms. We offer a full slate of employee benefits including: Competitive salaries Stock options 401(k) matching Medical, dental and vision coverage Four weeks of PTO accrued (vacation & sick time) annually + 11 company holidays Employer paid life insurance and long term disability Gym membership/recreational sports reimbursements Ossium Health provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, sex, national origin, age, disability, protected veteran status, sexual orientation, gender identity, gender expression, or any other protected characteristic. Our Equal Employment Opportunity Policy Statement and the Know Your Rights: Workplace Discrimination is Illegal Poster reaffirm this commitment. Pursuant to the San Francisco Fair Chance Ordinance, we will consider for employment qualified applicants with arrest and conviction records. If reasonable accommodation is needed, please contact our People Team at careers@ossiumhealth.com or 650-285-0603. Ossium Health complies with federal and state disability laws and makes reasonable accommodations for applicants and candidates with disabilities. Principals / direct applicants only please. Recruiters, please do not contact this job poster. Equal Opportunity Employer/Veterans/Disabled

Requirements

Must-haves

BS/BA in a technical field or equivalent experience
5+ years of manufacturing or related experience
3+ years in a formal people-leadership role
Working knowledge of aseptic technique, cleanroom operations, and cGTP/cGMP requirements
Experience owning deviations, investigations, and CAPAs, including root cause analysis
Excellent written and oral communication skills, with the ability to present results to cross-functional stakeholders
High level of attention to detail and the ability to operate with organization and urgency in a dynamic environment
Own daily HPC production output from donor intake through cryopreservation and initial inventory, ensuring every gift is used for its authorized purpose
Manage HPC Production Supervisors across shifts, ensuring processes are scheduled with appropriately trained and qualified personnel
Serve as operator, verifier, or trainer during clinical production as needed
Develop and report production metrics such as throughput, yield, right-first-time documentation, deviation rate, and cycle time, and drive action where targets are missed
Perform technical review of production batch records and ensure traceability of donor products through final disposition
Write and oversee event reports, investigations, risk assessments, and CAPAs, including effectiveness checks
Lead operational changes through project management, document creation, batch record revision, and risk assessment
Serve as hiring manager for HPC production roles and oversee onboarding, qualification, and ongoing training for the team
Serve as Core Team Leader for HPC, Marrow: own the Core Team charter, lead the daily meeting, set the agenda for weekly meetings, and drive cross-functional alignment across Production, Quality, Engineering, and MSAT
Accountable for the Core Team balanced scorecard covering safety, quality, process control and capability, variability reduction, throughput, supply chain planning, productivity, training, and equipment reliability
Keep the HPC process in control, capable, and compliant, prioritizing effectiveness before efficiency, and lead periodic formal process reviews and Annual Product Review feedback

Nice-to-haves

Advanced degree in a relevant scientific discipline
Direct experience managing teams in an aseptic manufacturing environment
Trained in statistical process control and continuous improvement tools and methodologies
Experience supporting FDA or other regulatory and accreditation inspections
Experience with process validation and technology transfer from development into routine production
Familiarity with lean or tiered daily management practices

Application prep

Use the role’s language and application details while tailoring your materials.

Platform: greenhouse
Effort: quick

Benefits

Benefits detected in the listing.

Dental

Vision

401(K)

Pto