quality control inspector salaries in los angeles, california

Ready to proactively identify problems with products and goods? In manufacturing and industrial environments, that’s what quality control inspectors do best. If you have what it takes to report and verify defects, troubleshoot on the fly and always operate with a safety mindset, your next career opportunity is waiting. Read on to learn more about the requirements for the role and how to apply. We’ll be sure to get back to you promptly.salary: $35,360 - $41,600 per yearshift: Firstwork hours: 6 AM - 2:30 PMeducation: No Degree RequiredResponsibilitiesInspecting output samples using industry-appropriate methods, such as comparing to standards, measuring dimensions and examining functionality Checking that the assembly or production line adheres to standards and procedures and complying with legal requirements Reviewing blueprints and specifications to compare to produced goods Recording inspection results by completing reports, summarizing re-works and wastes and inputting data into quality database Training the production team on quality control measures to improve product excellence Proposing improvements to the production process Monitoring the use of equipment to ensure it is safe and discard any that do not meet requirements Keeping measurement equipment operating accurately by following calibration requirements and calling for repairsSkillsQuality ControlProduct InspectionProduction ControlQuality AssuranceInspectionBlueprintsQualificationsYears of experience: 1 yearExperience level: Entry LevelRandstad is a world leader in matching great people with great companies. Our experienced agents will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. Whether you're looking for temporary, temporary-to-permanent or permanent opportunities, no one works harder for you than Randstad. Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.EOEDisclaime For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.

job summary: As the world's largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. Our partner recognizes the need for innovative care and utilizes Research & Development to further knowledge in Oncology, Neuroscience, Rare Diseases, and Gastroenterology. As a company that brings in over $30 billion in annual revenue, they have established themselves as a biopharmaceutical powerhouse that is changing the world. If you're looking for a position where your work will benefit millions of people, we are waiting for you! This role requires employees to be fully vaccinated against COVID-19 as a condition of employment, subject to a valid medical or religious accommodation.   location: Los Angeles, California job type: Contract salary: $25.84 - 30.39 per hour work hours: 9 to 5 education: No Degree Required   responsibilities: The primary responsibility of this role is to manage lab investigations and CAPA records in Trackwise.Role requires performing administrative duties such as collecting lab data, completing investigation records, filing timely extensions and progressing records through the action and effectiveness phases.Must be able to manage multiple records at once.Must be comfortable communicating with different departments to get updates on action items.Able to follow general writing template and receive feedback.Opportunity to develop and/or implement sustainable tracking system to manage records.Other responsibilities may include trending, data compilation, and other similar tasks as assigned.  qualifications: Must have strong organizational skillsMust have solid writing skillsMust have strong attention to detailTrackwise experience preferredPharmaceutical with laboratory background preferred***There is a lot of data gathering and must be efficient on the computer.***  skills: CAPA Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.Qualified applicants in San Francisco with criminal histories will be considered for employment in accordance with the San Francisco Fair Chance Ordinance. We will consider for employment all qualified Applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles' Fair Chance Initiative for Hiring Ordinance. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.

job summary: The Associate Scientist, Cell Manufacturing and Process Development will perform a broad range of tasks associated with the manufacture of cells for use in clinical and developmental studies. This resource will work as part of the team to execute Process Development Activities, plan and execute laboratory studies in order to support process development, characterization or process improvements   location: Pasadena, California job type: Contract salary: $35 - 40 per hour work hours: 9 to 5 education: Bachelors   responsibilities: Adheres to laboratory quality systems, batch records, SOPs, and cGMP regulations. Accurately completes documentation associated with development activities and sample analysis and records experiments in electronic lab notebook.Develops and executes protocols related to cell culture, processing and other activities as neededAssist with Technical Transfer of methods and procedures to the Cell Manufacturing departmentPerform analytical assays (ddPCR, CFU assay, Flow cytometry) to assist with Process developmentDrafts and reviews Standard Operating Procedures (SOPs), Batch Records, technical reports, and other documents for processes, equipment and test assays.Assists with testing and evaluation of new Equipment and commissioning.Assists with routine maintenance of scientific instrumentation, and equipment as required.Maintains current training status for all applicable activities.Provides feedback to Lead Scientist and ManagerPresents experimental data at departmental or project meetingsWorks well in a team environment, collaborates well with various colleagues in other groups such as Bioanalytics, QA and OperationsEnsures high safety standards are adhered to as governed by local, state and federal regulations, laws and policies   qualifications: BS/MA in life sciences (Cellular Biology, Immunology, or Biomedical)Familiarity with GMP Manufacturing processes and working within a controlled environment2+ years' experience in cell /gene therapy processing, familiarity with HSC is a plusExperience with analytical methods to characterize in process and final cell product samples (gene marking, CFU assay, flow cytometry)At least three years laboratory experience in biomedical research or a clinical laboratory with an emphasis on GMP practices, validation and execution of Laboratory SOPs and QC/QA practices. Experience in cellular biology, Immunology, Hematology and/or Hematopoietic Stem and Progenitor Cell Biology (HSPC) preferred.Experience in cell enrichment, culture, and cryopreservation of human HSPCs  skills: Cell Biology, Cell Cultures, GMP (Good Manufacturing Practice) Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.Qualified applicants in San Francisco with criminal histories will be considered for employment in accordance with the San Francisco Fair Chance Ordinance. We will consider for employment all qualified Applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles' Fair Chance Initiative for Hiring Ordinance. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.