Qc Salary at Picscout Inc BETA

QC Specialist I How You'll Make An Impact: Contribute to timely product release to meet the business goals to deliver product to customers on time by completing assigned tasks on time. Communicating technical issues and concerns promptly to escalate/establish root cause to move the process forward. Cross-training on our vast portfolio of processes to learn new lab skills while supporting equitable workload distribution and efficient product release. Identify areas for improvement in QC processes/procedures and execute projects to implement changes. Work on exciting new product implementation projects to train on and transfer robust processes for future QC testing of products. What the Candidate Brings: Bachelor’s degree in Molecular Biology, Biochemistry, Biotechnology, or related life science field. 1–2 years of relevant lab experience, preferably in a diagnostics, PCR testing, or regulated medical device/IVD environment. Understands and can apply GLP (Good Laboratory Practices) and G

Job ID: 25-07654 Job Title: Analyst, QC Critical Reagents Duration: 12 months, 40 hrs / week Location: Novato, CA SUMMARY The QC Critical Reagents Analyst is responsible for maintaining the *** Critical Reagents program for commercial products in the global network, including but not limited to reagent preparation, maintaining material inventory, generating technical documentation, and supplying materials to the global testing network. Materials in the Critical Reagents program include qualified reagents, reference standards, custom reagents, analytical cell banks and other important materials that require dedicated oversight. The individual prepares trend graphs and analyses for Critical Reagents to support routine requalification activities, regulatory responses, and investigational activities. RESPONSIBILITIES Responsible for critical reagent acquisition, preparation, and aliquoting. Coordinates qualification testing with laboratory personnel Coordinates and executes critical reagen

Job Description Job Description PCR QC Specialist I needed for a contract opportunity with Yoh Scientific’s client located in Hercules, CA. This position is for a molecular diagnostics manufacturer and the team is looking for candidates with a bachelor’s degree in life science, with 0-2 years of experience in a general lab environment performing analyses in the areas of chemistry, biochemistry, etc. Schedule: Monday – Friday, 8 am to 4:30 pm. Responsibilities A typical day will involve completion of testing on assigned batches and completing paperwork/data entry into SAP to document results for review/product release. This role requires communication and coordination between team members, the supervisor and the planners to ensure that we are keeping on top of priorities to avoid backorder. Besides routine testing, a day will include attending the daily Tier 1 meetings to report on safety, quality, delivery and inventory updates. Support Quality Control activities towards PCR reagents a

Job Title: Analyst, QC Critical Reagents Duration: 12 months, 40 hrs / week Location: Novato, CA SUMMARY The QC Critical Reagents Analyst is responsible for maintaining the *** Critical Reagents program for commercial products in the global network, including but not limited to reagent preparation, maintaining material inventory, generating technical documentation, and supplying materials to the global testing network. Materials in the Critical Reagents program include qualified reagents, reference standards, custom reagents, analytical cell banks and other important materials that require dedicated oversight. The individual prepares trend graphs and analyses for Critical Reagents to support routine requalification activities, regulatory responses, and investigational activities. RESPONSIBILITIES Responsible for critical reagent acquisition, preparation, and aliquoting. Coordinates qualification testing with laboratory personnel Coordinates and executes critical reagent distributions f

Job Description Job Description Job Title: QC Inspector – AOI/ AXI Job Function: Quality Control Job Overview: The Quality Control (QC) Inspector performs in-process to ensure adherence of the product to compliance requirements and procedures, operates AOI/ AXI machines and provides AOI AXI support. Reports to Production Supervisor and is in Newark, CA Primary Job Responsibilities 1.Operate the AOI/ AXI Responsible for the entire AOI/ AXI operation/line support activities Review AOI inspection for accurate, consistent detection of component placement and solder joint defects Support and maintain test handlers, troubleshooting AOI/ AXI machine whenever necessary to support production Assist superior to carry out various studies for quality improvement, program, and cycle time optimization for AOI / AXI operation. Work in close collaboration with the processing and engineering teams to improve visual defect yields and resolve processing issues 2. Perform inspections Perform visual qualit

Crusoe is building the World's Favorite AI-first Cloud infrastructure company. We're pioneering vertically integrated, purpose-built AI infrastructure solutions trusted by Fortune 500 companies to power their most advanced AI applications. Crusoe is redefining AI cloud infrastructure, with a mission to align the future of computing with the future of the climate. Our AI platform is recognized as the "gold standard" for reliability and performance. Our data centers are optimized for AI workloads and are powered by clean, renewable energy. Be part of the AI revolution with sustainable technology at Crusoe. Here, you'll drive meaningful innovation, make a tangible impact, and join a team that's setting the pace for responsible, transformative cloud infrastructure. About This Role: Crusoe is at the forefront of expanding hyperscale AI data center infrastructure and is actively doing so in Abilene, Texas and beyond. We have an opportunity for motivated construction professionals to be at th

Summary Join a leading company in delivering therapeutics for patients with serious and life-threatening rare genetic diseases. We focus on advancing therapies that are the first or best of their kind, targeting diseases that lack effective therapies and affect small numbers of patients, many of whom are children. Our Technical Operations group is responsible for creating drugs for clinical trials and scaling production for the commercial market. This team ensures regulatory standards are met and coordinates the worldwide distribution of our drugs to patients. Make a meaningful impact on patients' lives by joining our team. Responsibilities Responsible for critical reagent acquisition, preparation, and aliquoting. Coordinate qualification testing with laboratory personnel. Execute critical reagent distributions for the global testing network. Utilize LIMS to document acquisition and preparation of critical reagents, monitor testing status, and extract data for trend analyses. Generate

WHO WE ARE Arsenal Biosciences Inc. is a clinical-stage programmable cell therapy company engineering advanced CAR T-cell therapies for solid tumors. We seek a talented and experienced Sr. Manager, Quality Engineering & Validation (QA for QC) to work onsite based in our Hayward office. ArsenalBio's mission and purpose are very clear: defeat cancer. With our programmable and computationally driven approach, our team is engineering medicines to attack cancer's inherent multifaceted nature and overcome the challenges of addressing solid tumors with cell therapy. Driven by a collective of diverse experts across multi-scientific disciplines and clinical and manufacturing expertise, we are united in our purpose to develop the optimal medicines for improving patients' lives. This means you'll have the opportunity to work with the best talent in the field of cell therapy and be part of ONE TEAM, which advances therapies for patients who need it most. We are seeking a talented and motivated Sen