Quality Assurance Technician - Night Shift

Join Orca Bio, a pioneering late-stage biotechnology company, dedicated to transforming the lives of individuals battling blood cancer. Our mission is to redefine the transplant process through innovative next-generation cell therapies, significantly improving survival rates while minimizing risks associated with traditional methods, such as allogeneic stem cell transplants. We aim to restore not just patients' blood and immune systems but their lives. Our state-of-the-art manufacturing facility, spanning 100,000 square feet in Sacramento, CA, is crucial to advancing our clinical pipeline and ensuring the reliable delivery of our high-precision cell therapy products. As a key player in our Quality Assurance team, the Quality Assurance Technician will be instrumental in supporting the production of our life-saving therapies by ensuring compliance with stringent quality standards and cGMP regulations. This role involves direct oversight on the production floor, conducting real-time documentation reviews, and collaborating closely with manufacturing and technical teams to swiftly identify and resolve any issues. You will work alongside Manufacturing, Quality Control (QC), and other Quality functions to maintain seamless operations within a highly regulated environment.

Orca Bio is a pioneering biotechnology company dedicated to transforming the lives of individuals battling blood cancer. With over a million Americans currently affected, we are revolutionizing the allogeneic stem cell transplant process through our innovative cell therapies, which aim to significantly improve survival rates while minimizing risks associated with traditional methods. Our high-precision investigational cell therapies are designed to replace patients' blood and immune systems with healthier alternatives, ultimately restoring their quality of life.The Quality Control Technician - Night Shift plays a vital role in our cell therapy manufacturing facility by conducting both routine and non-routine testing to uphold the highest quality standards. Your contributions will be essential in ensuring the integrity and safety of our cell therapy products, directly impacting patient outcomes.

Role Overview Orca Biosystems is hiring a Quality Control Technician for the 1st shift in Sacramento, CA. This role focuses on upholding strict quality standards across products and materials. What You Will Do Perform tests and inspections on materials and finished products Analyze test data to verify compliance with quality requirements Document results and maintain accurate records Support adherence to industry regulations and internal protocols

Join the fight against blood cancer at Orca Bio, a pioneering late-stage biotechnology firm dedicated to transforming the transplant landscape. Our innovative next-generation cell therapies aim to significantly improve survival rates while minimizing risks associated with traditional allogeneic stem cell transplants. With our advanced and meticulously purified investigational cell therapies, we strive to not only replace patients' compromised blood and immune systems but also restore their quality of life.As a Quality Control Technician for Environmental Monitoring on Night Shift, your vital contributions will ensure the quality and sterility of our cell therapy manufacturing processes. You will be responsible for executing routine environmental sampling and microbiological testing to adhere to cGMP standards, thereby supporting the release of life-saving therapies. This is a hands-on position within a fast-paced, mission-driven team committed to precision, quality, and continuous improvement in a regulated manufacturing setting.

About Orca Bio Orca Bio is a late-stage biotechnology company focused on transforming the transplant process for patients with blood cancer. Our clinical manufacturing facility in Sacramento, CA, produces next-generation cell therapies designed to improve survival rates and reduce risks for patients in our trials. Role Overview The Quality Control Environmental Monitoring Technician helps ensure the safety and quality of our cell therapy products. This technician monitors environmental conditions in the manufacturing facility, supporting compliance with strict quality standards and regulatory requirements. Main Responsibilities Conduct routine and non-routine environmental monitoring and testing within the manufacturing facility. Follow established operating procedures for all testing and monitoring activities. Perform air and surface monitoring to maintain compliance with regulatory guidelines. Collect samples from critical areas throughout the facility. Maintain and calibrate environmental monitoring equipment to ensure accurate readings. Keep thorough records of all monitoring activities, including sampling plans, results, and any corrective actions taken. Carry out environmental analyses such as microbial and particulate matter testing. Perform basic laboratory functions, including reagent preparation. Location This position is based onsite at our clinical manufacturing facility in Sacramento, CA.

Join Essel Environmental as a Quality Control Inspection Technician specializing in video review. We seek detail-oriented individuals who are passionate about accuracy in video assessments, data entry, and mapping tasks.As part of our team, you will utilize your technical proficiency with CAD software, PDF editing tools, and video analysis software to ensure top-notch quality in inspections. Clear and professional communication with internal teams and clients is essential, as is effective time management to handle multiple projects.Preferred candidates will possess a background in Unearth, utility inspections, mapping, or CAD-related roles.

About Nivagen Pharmaceuticals:Nivagen Pharmaceuticals is a leading global company dedicated to enhancing health outcomes through the development of high-quality, affordable generic prescription medications and over-the-counter products tailored for the North American market. With over a decade of unwavering commitment to our core principles of excellence, integrity, and respect, our dedicated team collaborates effectively to promote advancements in manufacturing, distribution, and quality assurance, employing a comprehensive strategy to healthcare. We leverage vertical integration within the pharmaceutical supply chain, utilizing cutting-edge technology and maintaining a steadfast focus on excellence to continually improve access to and affordability of medications.We prioritize our employees' well-being through competitive compensation, comprehensive benefits packages, and robust training and development initiatives. By investing in our workforce and fostering a culture of growth and support, we empower our team to drive innovation and positively impact healthcare. At Nivagen, our mission is clear: to enhance lives by delivering high-quality, affordable medications while adhering to the highest standards of integrity and excellence.As a pioneer in pharmaceutical manufacturing, Nivagen is focused on producing sterile products that meet the stringent requirements of the healthcare industry. Our expertise lies in the production of vials, pre-filled syringes (PFS), and IV bags, and we strive to make a significant difference in patient care. Join us in pushing the boundaries of sterile manufacturing, achieving unparalleled standards in safety, quality, and operational efficiency.

Job Description:Join our dedicated team at Essel Environmental as a Quality Control and Assurance Specialist, where you will play a vital role in ensuring the highest standards of quality across multiple projects. Your responsibilities will include supervising and mentoring quality staff, leading quality training initiatives, and collaborating with senior management to uphold our corporate quality control program.Key Responsibilities: Oversee quality management across various projects to ensure compliance with industry standards. Supervise and develop the quality team, providing training on best practices and divisional requirements. Assist the Division Quality Manager in implementing and overseeing quality initiatives. Lead project teams through quality engagement processes, ensuring effective communication and collaboration. Gain in-depth knowledge of our corporate quality control programs, standards, procedures, and applicable building codes. Collaborate with project teams to develop and implement the Water+Min5 plan. Review and approve trade partner-specific Quality Control Plans in conjunction with the Division Quality Manager. Perform inspections and witness tests to assess work acceptability. Maintain accurate records of inspections, work performance, and related documentation. Work closely with Project Managers and Site Superintendents to manage site quality programs and address non-compliance issues. Assist in the preparation and implementation of quality control programs, including procedures and inspection instructions. Participate in internal and external quality audits to ensure adherence to quality standards. Assist in reviewing purchase orders and submittal documents for quality compliance. Help resolve project non-conformance issues effectively. Monitor subcontractor activities to ensure compliance with company standards and codes. Implement corrective measures in a timely manner. Document and assist in commissioning processes. Carry out any additional responsibilities as assigned.

Join Orca Bio, a pioneering biotechnology company dedicated to transforming the transplant process for blood cancer patients. Our mission is to develop next-generation cell therapies that significantly enhance survival rates while minimizing risks associated with traditional allogeneic stem cell transplants. By utilizing our high-precision investigational cell therapies, we aim to restore not just the blood and immune systems of our patients, but also their quality of life.The Material Handler - Night Shift plays a crucial role in the efficient management of pharmaceutical materials and products for our advanced cell therapy solutions. This position is responsible for ensuring compliance with stringent quality standards and regulatory requirements while executing processes related to warehouse inventory, kitting materials for production, and overseeing the intake, movement, and shipping of drug products and samples.Night Shift Hours:• 6:00 PM to 6:30 AM or• 6:30 PM to 7:00 AMSchedule:• Sunday, Monday, Tuesday + every other Wednesday or• Thursday, Friday, Saturday + every other Wednesday

At Orca Bio, we are on the forefront of redefining the allogeneic stem cell transplant process, aiming to enhance survival rates while minimizing associated risks. Our innovative approach focuses on next-generation cell therapies that not only aim to replace but also restore patients' blood and immune systems, ultimately improving their quality of life. We have established a cutting-edge 100,000-square-foot manufacturing facility in Sacramento, CA, dedicated to the reliable production of our high-precision cell therapy products, critical for advancing our clinical pipeline and ensuring the future availability of life-saving therapies. The Supervisor of Quality Control (QC) is vital to our mission, responsible for managing daily QC laboratory operations to ensure compliance with regulatory standards, internal protocols, and high-quality expectations. This role is essential in maintaining data integrity through meticulous audit trail reviews, leading investigations into out-of-specification (OOS) results, and ensuring the laboratory is always prepared for inspections.

Orca BioSystems seeks a Training Specialist to join the night shift team in Sacramento, CA. This role centers on developing and presenting training programs aimed at building staff skills and knowledge. Role overview The Training Specialist will design and deliver learning sessions that help employees perform at their best. By supporting staff development, this position plays a key part in upholding strong service standards and consistent operational quality across the organization. What you will do Create and implement training materials tailored to staff needs Lead training sessions during the night shift Support efforts to maintain high-quality operations and service Location and schedule This is an on-site role based in Sacramento, CA, working during night shift hours.

Join Orca Bio, a pioneering late-stage biotechnology company committed to transforming the lives of patients fighting blood cancer. Through our innovative and next-generation cell therapies, we aim to enhance survival rates and minimize risks associated with transplants. Our mission is to provide patients with healthier blood and immune systems, ultimately restoring their quality of life.The Night Shift Supervisor of Materials and Cold Chain Operations will oversee the daily activities linked with material supply, handling, cryogenic storage, and the packaging and shipping of our cell therapy drug products. This critical role will ensure that all operations comply with Good Manufacturing Practices (GMP), guaranteeing the safe, accurate handling, storage, and distribution of materials and drug products in alignment with regulatory guidelines and internal protocols.As a supervisor, you will lead a dedicated team of material handlers and cryogenic processing specialists, ensuring operational efficiency, maintaining inventory control, and facilitating the timely shipment of vital materials and patient-specific drug products.

Role overview Cornerstone Building Brands seeks a Quality Assurance Manager for its Sacramento manufacturing facility. This position leads quality assurance activities and ensures that products meet established quality and compliance standards at all times. Key responsibilities Lead quality assurance initiatives throughout manufacturing operations Collaborate with cross-functional teams to design and implement quality control processes Carry out audits to confirm adherence to compliance and product requirements Encourage ongoing improvement in quality procedures and practices Work location This position is onsite at the Sacramento facility.

Orca Bio develops precision cell therapies for blood cancer, with a focus on improving allogeneic stem cell transplants. The Sacramento, CA site plays a critical role in manufacturing these therapies and supporting clinical trials. Role overview The Quality Assurance Specialist (Day Shift) helps maintain high standards for product safety and compliance. This position manages key quality systems and ensures that each batch meets required specifications before release. What you will do Oversee quality systems, including deviation management, change controls, CAPA (corrective and preventive actions), and document management Review and manage production records Make timely batch disposition decisions to uphold quality standards before product release Support efficient processing timelines for cell therapy products Impact This role directly supports the delivery of safe, high-quality cell therapy products to patients in clinical trials, helping Orca Bio advance its mission and meet critical timelines.

About Orca Bio Orca Bio is a late-stage biotechnology company focused on transforming stem cell transplants for blood cancer patients. The team develops next-generation cell therapies designed to improve survival rates and reduce risks like graft versus host disease. With a 100,000-square-foot manufacturing facility in Sacramento, CA, Orca Bio supports both clinical trials and future commercial distribution of its therapies. Role Overview: Quality Assurance Specialist (Weekend Shift) This Quality Assurance Specialist role covers the weekend shift: Friday through Monday. The position plays a key part in maintaining Orca Bio’s quality policy and ensuring that cell therapy products meet rigorous standards before release. What You Will Do Manage and maintain quality systems, including production records and deviation management Oversee processes for deviations, change control, and corrective and preventive actions (CAPA) Handle document management to ensure accurate and compliant record-keeping Make timely batch disposition decisions to support rapid product processing and release Help uphold compliance with internal quality standards and regulatory requirements Location and Shift Details Location: Sacramento, CA Schedule: Friday through Monday (weekend shift) Impact This role directly supports the delivery of innovative cell therapies, contributing to better outcomes for patients facing blood cancers. Learn More For more on allogeneic stem cell transplants, see the Mayo Clinic overview.

Xometry (NASDAQ: XMTR) is revolutionizing manufacturing by connecting innovative thinkers with capable manufacturers who can turn their visions into reality. Our digital marketplace provides manufacturers with essential resources for growth while simplifying access for Fortune 1000 companies to global manufacturing capabilities.As a Supplier Quality Engineer, you will thrive in a fast-paced environment where your expertise in problem-solving and continuous improvement will be pivotal in enhancing quality metrics. This prominent role involves leading Supplier Quality initiatives while collaborating with internal departments and our supplier network to ensure the delivery of top-quality products.Your daily responsibilities will encompass a wide range of quality-focused activities with partners, guiding products from initial concept through to full-scale production within Quality Assurance. You will interact with various internal teams, including DFM Engineering, Quality, Case Management, and Partner Management, alongside a diverse array of partners specializing in CNC machining, sheet metal fabrication, additive manufacturing, and injection molding.If you excel in navigating ambiguity and are committed to establishing standardized processes, we encourage you to apply for this opportunity!

As the Director of Statewide Quality for California Medicaid, you will be at the forefront of enhancing healthcare quality across the state. You will lead initiatives aimed at improving patient outcomes and ensuring compliance with Medicaid standards. Your role will involve collaborating with healthcare providers, managing quality improvement programs, and utilizing data analytics to drive decision-making.

Join our team at AWP Safety as a Traffic Control Flagger, where you will play a vital role in ensuring the safety and efficiency of traffic flow in construction zones. As a part-time employee, you will be responsible for directing vehicles and pedestrians, setting up traffic control devices, and communicating effectively with team members and the public.

About Nivagen Pharmaceuticals: Nivagen Pharmaceuticals is a pioneering global organization focused on improving lives through the development and supply of affordable generic prescription medications and over-the-counter products tailored for the North American market. For over a decade, we have upheld our core values of excellence, integrity, and respect for individuals. Our dedicated team works collaboratively to drive advancements in manufacturing, distribution, and quality control, ensuring a comprehensive approach to healthcare. By leveraging vertical integration of the pharmaceutical supply chain, cutting-edge technology, and a steadfast commitment to quality, we aim to redefine medication accessibility and affordability. We prioritize the well-being of our employees by offering competitive compensation, comprehensive benefits, and extensive training and development opportunities. At Nivagen, we are committed to making a lasting impact in healthcare by delivering high-quality, affordable medications while maintaining the highest standards of integrity. Job Overview: We are looking for a skilled and dedicated Technician to join our Engineering and Maintenance team at Nivagen Pharmaceuticals. In this essential role, you will operate and maintain our HVAC, Building Management System (BMS), and Energy Management System (EMS), ensuring their safe, efficient, and reliable operation. Your contributions are vital in minimizing downtime and enhancing the overall productivity of our manufacturing operations. Key Responsibilities: Operate and maintain HVAC, BMS, EMS, and associated systems while adhering to all safety protocols and regulations. Monitor HVAC systems to identify malfunctions and schedule necessary maintenance. Conduct routine inspections and maintenance on HVAC systems to ensure optimal performance. Document and maintain daily records regarding HVAC operations, maintenance, and safety activities. Coordinate with the maintenance team to facilitate repairs and improvements. Comply with all environmental policies and regulations to ensure legal compliance. Possess knowledge related to clean room classification, Air Handling Unit (AHU) zoning, pressure balancing, and related systems.

About Nivagen Pharmaceuticals LLC Nivagen Pharmaceuticals LLC develops and distributes affordable generic prescription and over-the-counter medications for the North American market. For over a decade, the company has focused on excellence, integrity, and respect. Teams at Nivagen collaborate across manufacturing, quality control, and distribution, with a commitment to improving access to essential medicines. Vertical integration and advanced technology support the company's mission to deliver high-quality products. Nivagen values its employees, offering competitive pay, comprehensive benefits, and training for professional growth. Location Sacramento, CA 95834 Role Overview: Visual Inspection and Packing Operator The Visual Inspection and Packing Operator plays a key part in maintaining product quality at Nivagen. This position involves hands-on inspection of products, operating leak testing machines, and running packing equipment to prepare shipments. The operator may participate in sterile manufacturing processes and must consistently follow company policies, standard operating procedures, regulatory guidelines, and current Good Manufacturing Practices (cGMP). Attention to detail and a strong commitment to safety and quality are essential in this role.