Supervisor, QC Salary at Ecc Ltd BETA

About the Company Join a newly-established in-house QC team at a growing biologics company in Redwood City, CA. Collaborate with teammates to continue developing and building out the new in-house QC testing lab. As a senior team member, in addition to conducting QC analysis benchwork, contribute via QC protocol development, overseeing outsourced QC testing, review of method transfer/ method qualification, leading QC-related QMS activities, and more. Responsibilities Serve as a team proficiency expert for ddPCR (droplet digital PCR) and other molecular based and cell based QC assays for batch release, stability testing, and product characterization purposes. Review internal GMP analytical testing and method qualification. Collaborate with Analytical Development on assay development and troubleshooting. Provide oversight for external QC testing at third party labs / CMO. Develop QC protocols and SOPs as needed. Lead Lab deviation investigations, CAPAs, change controls and other QMS activ

Triple Ring Technologies, Inc. offers a unique environment for talented individuals interested in undertaking varied technical challenges, primarily in medical device and life science industries. Headquartered in Newark, CA, we are an innovative research and development company that partners with clients to deliver complex technical solutions. Our highly interdisciplinary team includes senior professionals from industry, finance, and academia, with extensive experience in medical device, life science, clean tech, security, and industrial technologies. We rely upon each other for technical excellence, real-world engineering and commercial wisdom. Learn more at www.tripleringtech.com. Job Summary The Manager of Quality Assurance will maintain and lead the implementation of Triple Ring's Quality Management System (QMS) for client projects. He/she will work collaboratively with project leadership and other team members to develop, coordinate, and own the QMS elements of a project. These wi

Overview Currently offering a unique opportunity for a QC Professional to join a team with key responsibilities in QC microbiology. Initial duties will include supporting environmental monitoring incubation, reading and reporting of data. Future roles may also incorporate performing environmental monitoring sampling in our CGMP cleanrooms. Other duties include laboratory upkeep, media growth promotion, gram staining and data entry. The qualified candidate will collaborate closely with manufacturing team members and will require working in cGMP cleanrooms and QC labs. Responsibilities • Media growth promotion • Processing of environmental monitoring sampling that include sampling, incubation and reading of media plates • Aseptic gowning qualification • Bioburden • Gram staining • Subculture and coordination of the shipment of isolates for microbial identification • Gas testing • Raw materials sampling and testing • Equipment cleaning and maintenance • Laboratory upkeep and inventory man

QC Inspector (In Process, Final, Source) Job purpose Perform inspection activities in the following areas; Incoming Inspection electrical and mechanical, In-process and Final areas of product. Inspect, audit, and report the quality level of incoming and outgoing products, ensuring that all customer quality requirements are being met such as: appearance, fit, form, function; including on time delivery of shipments. Reject and isolate defective part/s and accurately complete all associated paperwork and data entry with non-conforming reports. Perform duties according to IPC 600, IPC 610 and or J-Std-001 and J-Std-001 Space addendum (latest revisions) and our Quality System work instructions. Properly interpret customer documentation, drawings/blue prints, Bills of Material (BOM), datasheets and specifications and other documents necessary to perform inspection duties. Must be available to work over-time. Cross-train in other areas or perform other duties as required, by the Quality Super

Work Schedule Standard (Mon-Fri) Environmental Conditions Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Cleanroom: no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair etc... allowed, Laboratory Setting, No contact lens allowed; prescriptive glasses will be provided, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.), Will work with hazardous/toxic materials Job Description As part of the Thermo Fisher Scientific team, you'll discover meaningful work that positively impacts a global scale. Join our colleagues in bringing our Mission to life daily to enable our customers to make the world healthier, cleaner, and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world's toughest challenges, like protecting the environment, ensuring ou

Who We Are Arcellx isa public, clinical-stage biotechnology company reimagining cell therapy by engineering innovative immunotherapies for patients with cancer and other incurable diseases. We believe that cell therapies are one of the forward pillars of medicine and our mission is to destroy cancer and advance humanity by developing cell therapies that are safer, more effective, and more broadly accessible. Our team members are made up of talented innovators and dreamers working from our offices in Rockville, Maryland, and Redwood City, California. At Arcellx, we hire exceptional people and create a fun, diverse, supportive, and informal environment that allows everyone to do their best work. What Matters to Us Living our core values is essential to maintaining a work environment that is high-performing, inclusive, and collaborative. We look for candidates who demonstrate strong values alignment and bring different backgrounds, viewpoints, and abilities to the team. Arcellx Core Value

Position Summary We are seeking an innovative and highly motivated Manager for Manufacturing to join our team who will be responsible for ramp-up and oversight of the cGMP operations within a state-of-the-art multi-product cell therapy manufacturing facility that will be utilized to manufacture autologous and allogeneic cell therapy products. This individual will partner with other functions to produce cell therapy products through safe and compliant manufacturing operations according to cGMP requirements. As such, the role will require proven leadership to drive effective communication, coordination, and collaboration across relevant cross functional groups to ensure robust production, testing, and release of product to patients. This is a multidisciplinary role & this individual will need the ability to interface with all levels of the organization, including Commercial, Quality, MSAT, QC, Process/Analytical Development, Supply Chain, Warehouse, Training, Engineering/Facilities, EH&S

**General** **Description:** This role will support the GPS Safety Operations to enable process efficiency, quality and compliance. This role is responsible for supporting the oversight of ICSR data quality and compliance with global PV legislation. This role is additionally responsible for supporting analysis of processes across GPS Safety Operations, deriving actionable insights, and supporting the implementation of improvement plans. Further, this role collaborates with GPS ICSR Management and GPS Quality Operations teams in order to ensure appropriate documentation is completed in the context of ICSR data quality, ICSR submissions compliance and ad hoc identification of potential automations or other systems enhancements to increase bandwidth and relieve cognitive load from associated teams. **Essential Functions of the** **Job:** **Process Excellence** **Support** + Support identification and monitoring of GPS Key Performance Metrics & Key Compliance Metrics + Support collaboratio