Orca Bio

You'll partner with front-line and mid-level managers to **build leadership capabilities** and operationalize People Team initiatives at manufacturing sites. Your core impact will be driving **effective people management practices** and fostering a positive, inclusive culture. This role stands out for its focus on **biotech/pharma manufacturing** and hourly workforce support.

You'll serve as the primary liaison between Orca Bio and hospital Authorized Treatment Centers, building key relationships and supporting site readiness. You'll **drive onboarding activities** for groundbreaking cell therapies and **streamline activation timelines**. This field-based role offers high impact in bringing **novel therapies to patients**.

You'll perform analytical testing to ensure the highest quality standards in a **cell therapy manufacturing facility**. Your work will directly impact the **safety and integrity** of life-saving products. This role offers the opportunity to work with **advanced biotechnology** in a GMP-regulated environment.

You'll oversee **facility operations** and **GMP compliance** for a biotech site. You'll manage utility systems, service providers, and preventive maintenance programs to ensure seamless production support. This role offers the chance to **lead critical infrastructure** in a cell therapy environment.

You'll supervise a team producing **cell therapy products** in a **cGMP-compliant cleanroom**, ensuring quality and regulatory compliance. Your leadership directly impacts **Oncology drug manufacturing**.

You'll oversee daily operations for material supply, cryogenic storage, and cold chain shipping of cell therapy drug products at a late-stage biotech company. You'll lead a team of material handlers and specialists to ensure GMP-compliant handling and timely delivery of patient-specific therapies. This role offers the chance to **impact cutting-edge cell therapies** in a **GMP-regulated environment**.

You'll monitor clinical studies for Orca Bio, ensuring trials comply with protocols and regulations. Your work directly impacts patients fighting blood cancer by improving transplant outcomes. This role offers **remote flexibility** with travel for **site visits**.

You'll operate **advanced manufacturing equipment** to produce **cutting-edge cell therapy products** in a GMP cleanroom environment. You'll ensure adherence to strict quality standards and aseptic techniques while collaborating with cross-functional teams.

You'll lead **cross-functional strategic initiatives** for the CEO and President at a **biotech company approaching commercialization**. Your work will directly shape the company's growth by improving organizational effectiveness and execution. You'll transition between long-term strategy and daily operations, ensuring alignment across the executive team.

You'll serve as medical lead for Orca-Q, a next-generation cell therapy program targeting non-malignant diseases and autoimmune indications. You'll design and execute Phase 1 studies, analyze data, and collaborate with investigators nationwide to drive the program toward registration. This role offers the chance to shape early clinical strategy at a late-stage biotech company.

You'll lead **analytical development for cell therapy programs**, overseeing **flow cytometry and method validation**. Your work will directly impact **regulatory submissions and commercialization**. The role offers a chance to shape strategy and mentor a scientific team.

You'll lead **GMP testing operations** for **cell therapy products** and oversee QC workflows, investigations, and regulatory inspections. Your impact ensures product quality and compliance with cGMP standards.

You'll lead **clinical trial data management** for a late-stage biotech developing **next-generation cell therapies**. You'll ensure data accuracy and CDISC compliance from study start-up to database lock, directly impacting safer transplant options for blood cancer patients.

You'll lead **talent acquisition strategies** for Orca Bio's manufacturing operations in Sacramento, acting as program lead and mentor for a team of contract recruiters. You'll directly own full-lifecycle recruitment for hard-to-fill technical and leadership roles, driving employer branding and optimizing ATS workflows.

You'll lead the **promotional launch of Orca-T** for Orca Bio, a late-stage biotech redefining blood cancer transplant. Your work will drive **HCP engagement strategies** and **omnichannel tactics** to maximize market penetration.

You'll oversee a team producing **cell therapy products** for a late-stage biotech company. Your leadership ensures compliant, on-schedule manufacturing that supports **life-saving treatments for blood cancer patients**.

You'll play a critical role in producing **life-saving cell therapy products** for a **late-stage biotechnology company**. You'll operate advanced manufacturing equipment and adhere to strict quality standards in a cleanroom environment. Orca Bio offers the opportunity to redefine transplant processes.

You'll support **cryopreservation and shipment** of **cell therapy products** for a late-stage biotech company. You'll ensure chain-of-identity and chain-of-custody for patient materials. This role offers **night shift schedule** in a **GMP-regulated environment**.

You'll introduce yourself to our Recruiting Team for potential future roles at Orca Bio, a late-stage biotechnology company redefining **cell therapy** with high-precision investigational treatments. This application helps us match your skills to upcoming opportunities in our Bay Area and Sacramento sites.

You'll oversee night shift operations for **material supply**, **cold chain management**, and **cGMP-compliant shipping** of cell therapy drug products at a late-stage biotech company. You'll lead a team ensuring **chain-of-identity and chain-of-custody controls** for patient-specific materials. This role directly impacts patients receiving life-saving cell therapies.

You'll improve the **efficiency and safety** of **cell therapy manufacturing processes** for a late-stage biotech. You'll manage product life cycles, process monitoring, and troubleshooting to support clinical and commercial delivery.

You'll oversee daily QC lab operations at a **late-stage biotech company** redefining stem cell transplants. You'll manage a team, ensure **cGMP compliance**, and lead investigations to support life-saving cell therapies.

You'll design KOL engagement strategies and shape brand tactics for a late-stage biotech launching next-gen cell therapies. Your insights will directly influence positioning and messaging to improve survival rates for blood cancer patients. This role offers the chance to lead market development in a high-impact therapeutic area with extensive cross-functional collaboration.

You'll oversee daily GMP manufacturing operations for cell therapies at Orca Bio's state-of-the-art facility in Sacramento, CA. You'll ensure consistent delivery of patient batches with high safety and quality standards while leading a team of Supervisors. This role directly impacts patients with blood cancer by advancing precision cell therapies.

**You'll** provide **real-time QA oversight** in a **cGMP manufacturing facility** producing life-saving cell therapies. Your work ensures compliance and product quality for patients fighting blood cancer. This night-shift role at a late-stage biotech offers direct impact on clinical and commercial products.

You'll lead a team of MSAT process engineers within a commercial cell therapy manufacturing facility. Your work will ensure product quality, efficiency, and compliance for life-saving therapies. **Lead process improvements** and **support tech transfers** in a state-of-the-art facility.

You'll handle materials and inventory for cell therapy products in a GMP cleanroom environment. You'll ensure efficient storage, distribution, and kitting of pharmaceutical materials. This role impacts **life-saving therapies** for **blood cancer patients**.

You'll oversee day-to-day operations and maintenance at a **biotechnology company** developing next-generation cell therapies. Your core impact is ensuring a **GMP-compliant facility** with reliable systems and regulatory adherence. This role offers the chance to work in a **cutting-edge cell therapy environment**.

You'll join Orca Bio's **night shift team** ensuring the **highest quality standards** in cell therapy manufacturing. You'll perform critical analytical tests that directly impact patient safety and product integrity, working in a regulated environment with cutting-edge biotech.

You'll perform routine and non-routine analytical tests to ensure **high quality standards** in a **cell therapy manufacturing facility**. Your work will play a crucial role in maintaining the integrity and safety of **life-saving cell therapy products**.

You'll manage **quality systems** for a late-stage biotech company developing next-generation cell therapies. You'll ensure batch disposition and compliance with **FDA regulations** in a state-of-the-art manufacturing facility. This role directly impacts the lives of patients fighting blood cancer.

You'll manage quality systems including deviations, change controls, and batch disposition for **cell therapy products** at a **late-stage biotechnology company**. You'll ensure compliance with regulatory standards and support the rapid release of therapies for patients in clinical trials.

You'll develop and deliver training programs for GMP manufacturing operations at a late-stage biotech company. You'll directly impact the **quality and safety** of cell therapies for blood cancer patients. This role offers the chance to work in a **state-of-the-art facility** on **life-saving therapies**.

You'll oversee **cell therapy production** at a **clinical manufacturing facility** in Sacramento, ensuring adherence to **cGMP standards**. Your leadership ensures timely, compliant manufacturing for patients in clinical trials.

You'll **lead key elements** of a **pre-commercial compliance program** for a late-stage biotech company developing next-generation cell therapies. Your work will directly impact the safe and ethical delivery of life-saving treatments to patients fighting blood cancer.

You'll lead cost accounting for a **late-stage biotech company** developing next-generation cell therapies. You'll **oversee manufacturing cost structures** as the company scales from clinical-stage to commercialization. This role offers **direct impact on saving lives** through precision cell therapies.

You'll lead **cost accounting** activities for manufacturing and operational functions at a late-stage biotechnology company redefining cell therapies. Your core impact will be overseeing product costing, inventory valuation, and COGS reporting, while **supporting business scaling** from clinical-stage through commercialization. This role requires **deep expertise in manufacturing cost structures** and cross-functional leadership.

You'll perform routine and non-routine analysis of cell therapy products at a **late-stage biotechnology company** redefining the transplant process. Your work ensures the consistent delivery of **life-saving therapies** to patients fighting blood cancer. You'll collaborate with cross-functional teams in a **cGMP-regulated environment**.

You'll improve the efficiency and safety of **drug product manufacturing** for a late-stage biotech company developing **next-generation cell therapies**. Your work will help deliver life-saving therapies to patients with blood cancer.

You'll lead **cell therapy manufacturing processes** at a late-stage biotech company. Your core impact is improving efficiency and safety in drug product manufacturing. You'll oversee **process monitoring and troubleshooting** for clinical and commercial products.