Chemical Operator Salary at Yahoo BETA

IDR is seeking a Quality Assurance Specialist IV to join one of our top clients in Newark, CA. This role is perfect for individuals with a strong background in biology, biochemistry, or a related pharmaceutical-biotechnology discipline, and a minimum of 3 years of experience in a GMP environment. If you are looking for an opportunity to join a large organization and work within a team-oriented culture, please apply today! Position Overview/Responsibilities for the Quality Assurance Specialist IV: Provide compliance support or oversight for operational functions Conduct investigations for Laboratory Investigation Reports (LIR) and deviations via effective root cause analysis Author and revise controlled documents such as procedures, methods, work instructions, protocols, and reports Perform risk analysis as needed to determine severity, likelihood of recurrence when triaging events and/or conducting investigations Manage and author change controls related to qualification, modification,

Job Description Job Description Essential Functions: · Performs visual, dimensional and functional inspection and testing according to documented policies and procedures. · Records inspection and test data as prescribed by written instructions and procedures. · Operates all associated test and measurement equipment as instructed and as documented in procedures. · Recommends changes to policies and procedures. · May prepare and submit change requests. · Documents non-conformances in Non-Conforming Material Review system. · Participates in GR&R studies as directed by engineers or technicians. Collects data for First Article inspections. · Performs testing and inspection in accordance with special test requests. · May train other Inspectors. Assists in gathering, analysing, and trending of data Other. · Duties: Performs work of a miscellaneous nature as required. Support all Divisional initiatives as identified by divisional management and in support of Quality Management Systems (QMS), E

The Quality Control Analyst is responsible for providing hands on support of quality control testing activities POSITION DUTIES & RESPONSIBILITIES: 1. Provide a hands on capacity for the performance of routine QC FVIII ELISA , Electrophoresis, qPCR Laboratory logistical and testing activities 2. Perform FVIII HTRF testing to support the release of commercial drug product 3. Perform all laboratory activities in a manner consistent with cGMP requirements 4. Keeps accurate documentation and follow relevant SOPs 5. Operate automated analytical instrumentation (includes preventive maintenances and troubleshooting) 6. Perform routine lab bench work in a team environment 7. Evaluate data, write technical report and participate in lab investigations Preferences: * Experience with automated equipment and analytical test methods * Strong computer and communication skills required * Ability to work in a team environment * Experience with ELISA/HTRF/plate based assays/gels preferred * Experience d

Job Summary This position is responsible for a combination of functions within the quality business unit, including device history record review and release, document control, training, receiving, incoming inspection, and final release testing. Job Details/Responsibilities Documentation: Prepare documentation in accordance with Quality Management System requirements. This includes, but is not limited to, document change orders, lab notebooks, testing results, etc. Maintain all Incoming quality assurance records, quality assurance release logs, equipment files, and databases, e.g., inspection records, and nonconformances, etc. Device History Records (DHR) / Product Release: Review and release device history records and product release documentation to ensure compliance with quality system requirements and within electronic database software (e.g., SAP). Notify management regarding discrepancies or irregularities. Maintain hard copy files. Monitor and report trending data monthly within

Job Description: Job Title: Quality Control Analyst Location: Berkeley CA 94710, Onsite Duration: 12-month contract (Extendable). Hourly Pay: $28/hr to $32/hr on W2 without benefits on W2 Schedule: Mon - Fri, Business hours Job Description: Responsible for biological and chemical evaluation of final products, intermediate products, raw materials, and production facilities. • Duties include performing QC assays, writing and establishing specifications, assisting in the validation of QC assays, and writing Standard Operating Procedures. • Has knowledge of commonly used concepts, practices, and procedures within a particular field. • Relies on instructions and pre-established guidelines to perform the functions of the job. Works under immediate supervision. • Typically reports to a supervisor or manager. 4-6 Years of Experience INTAKE QUESTIONS: • What is a day like in this role? From a candidate’s perspective, what’s exciting about this role and team? What does this role accomplish for t

Chemical Operator Shift: Monday - Friday 7am - 3:30 pm Pay Rate: $26.68. NOTE: Interviews are held virtually Monday - Thursday only. The individual will be responsible for supporting and leading the technical demands of the site gas or chemical equipment. They will ensure compliance with operation and maintenance procedures, and emergency preparedness, and drive flawless execution. A subject matter expert for gas, chemical, and slurry equipment, providing technical support and problem resolution. The individuals will be a part of the onsite Project and equipment team and will support the gas and chemical operations in 11 buildings throughout Santa Clara and Sunnyvale. The Technician will support and lead the technical challenges for over 2000 pieces of distribution equipment of various types and vendors. You will ensure compliance when writing, editing, and executing operating and maintenance procedures and drive a ZERO safety or quality incident culture. A subject matter expert for ga

We are seeking a Quality Assurance Specialist to join a client in Hayward. The role is with a health and nutrition services client. This is a temp-to-hire position. This is a 100% onsite position. Hours are Monday - Friday 8:00 am - 4:30 pm with a starting pay of $25-$28 an hour. Job Duties: Coordinate with client lab to ensure that specifications are accurate before being sent for testing. Verify invoices match test prices. Manage and track QC tests after they are received and sending to the lab. Obtain PO's from accounting for tests. Coordinate tests. Be the internal point of contact to relay test results. File reports on QC. Communicate with vendors on tests and maintenance. Follow lab safety practices. Organize samples. Requirements: Bachelor's Degree preferred or Associate's Degree Chemistry background a plus. Strong MS Office and computer skills. Ability to lift up to 25 lbs. All qualified applicants will receive consideration for employment without regard to race, color, nationa

VIA Technologies, Inc. a rising leader in utilizing advanced AI, IoT, and computer vision technologies for the transportation safety applications. Headquartered in Taipei, Taiwan, VIA’s global network links the high-tech centers of the US, Asia, and Europe, and spans a customer base that includes many of the world’s leading hi-tech, industrial, and transportation companies. ESSENTIAL DUTIES AND RESPONSIBILITIES: • Production Management (high mix low volume for US team customer trial): Oversee the production process, ensuring that manufacturing operations meet production targets, quality standards, and delivery deadlines. Coordinate with production teams to optimize workflow, minimize downtime, and address any issues that arise during production. • Inventory Control: Manage inventory levels for both raw materials/components and finished goods in the warehouse. Implement inventory control procedures to optimize stock levels, minimize carrying costs, and prevent stockouts or overstock sit