Laboratory Technician Jobs in Azusa, CA

Create a healthier, brighter future for pets, pet parents and people! If you want to make a real difference, create an exciting career path, feel welcome to be your whole self and nurture your wellbeing, Petco is the place for you. Our core values capture that spirit as we work to improve lives by doing what's right for pets, people and our planet. We love all pets like our own We're the future of the pet industry We're here to improve lives We drive outstanding results together We're welcome as we are Petco is a category-defining health and wellness company focused on improving the lives of pets, pet parents and Petco partners. We are 29,000 strong and operate 1,500+ pet care centers in the U.S., Mexico and Puerto Rico, including 250+ Vetco Total Care hospitals, hundreds of preventive care clinics and eight distribution centers. We're focused on purpose-driven work, and strongly believe what's good for pets, people and our planet is good for Petco. We Invite You Unleash your career. We're a health and wellness company. Our mission is to improve the lives of pets, pet parents and each other. Vetco Total Care Hospital Medical Leaders ensure the highest level of patient care and client experience, drive continuous improvement in clinical skills and cultivate a supportive, respectful, and collaborative work culture where all people feel welcome. Hospital Medical Leaders review hospital P&L and partner with medical and operations field leaders to drive hospital performance, efficiency and exceptional care quality. Vetco Total Care hospitals are fully equipped with the latest technology including cloud-based practice management and records software, digital and dental x-ray, Idexx, Butterfly iQ+ handheld ultrasound, Vetology Radiograph Interpretation AI, VMED Vet-Dop2 Doppler Blood Pressure System and VETSCAN IMAGYST enabling you and your team to deliver the highest standards of care. This includes routine, diagnostic and complex procedures including (but not limited to) radiographs and ultrasounds, dental extractions and prophylaxis, spays/neuters, abdominal exploratory, and mass removals. You will grow as a practitioner and a leader with paid continued education and leadership training. With the freedom to practice true autonomous medicine, you will utilize all your experience and skills and continue to learn. You will build relationships with pet parents and model respect and empathy. You will enjoy the support of local medical directors and a team of licensed and trained veterinary technicians and assistants. Plus, flexible schedules, open time off, zero noncompetes and no on-call shifts ensure you enjoy your life outside of work. We Support You Financial Wellbeing Competitive salary 401(K) and company match Production and quarterly bonuses Sign-on and relocation bonuses for many roles Generous discounts in store, grooming, training, hospital services - plus travel, entertainment, insurance, and fitness perks Opportunity to invest in stock options and receive stock shares/LTI Work-Life Sustainability Open- and paid- time off with no negative accruals Flexible schedule options No on-call, no late nights or overnights Health & Wellness Support Comprehensive medical, dental, vision and mental health insurance and resources for you and your loved ones Fertility and family-planning assistance Paid parental leave Pet bereavement Career Growth No noncompetes for veterinarians we hire No sales quotas on wellness plans $3500 paid CE for full-time veterinarians 100% DEA reimbursement Subject Matter Expert training in dentistry, dermatology, and nutrition Mentorship available Medical leadership and business training Career advancement opportunities Petco Animal Supplies, Inc. is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, age, protected veteran status, or any other protected classification. The pay ranges outlined below are presented in accordance with state-specific regulations. These ranges may differ in other areas and could be subject to variation based on regulatory minimum wage requirements. Actual pay rates will depend on factors such as position, location, level of experience, and applicable state or local minimum wage laws. If the regulatory minimum wage exceeds the minimum indicated in the pay range below, the regulatory minimum wage will be the minimum rate applied. $126,880.00 - $202,800.00 / year For a more detailed overview of Petco Total Rewards, including health and financial benefits, 401K, incentives, and PTO -see ******************************************** To translate this webpage to Spanish or other languages on your internet browser click the translate button to the right of your browser address bar. Additional instruction can be found here: ************************************************************************************ Para traducir esta página web al español u otros idiomas en su navegador de Internet, haga clic en el botón de traducción a la derecha de la barra de direcciones de su navegador. Puede encontrar instrucciones adicionales aquí: ************************************************************************************

Our client is a major refinery in the Los Angeles area serving the fuel transportation and aviation fuel needs of the western United States. Operates an integrated network of strategic assets that creates and sells refined petroleum products, from feedstock acquisition to wholesale, commercial and retail sales outlets. They have an immediate need of Laboratory Technician/Chemist to work in their Lab. Under the general direction of the Laboratory Superintendent, responsibilities include, but may not be limited to: Adherence to safe work practices Performing chemicals analyses and quality control testing in the Chemical Laboratory using accepted, published procedures Performing calibrations and standardization to maintain quality in test results Understanding and utilizing SQC tools Reviewing / updating procedures Assisting in or performing maintenance on instrumentation Interacting with Area Supervisors, Unit Engineers or Unit Operators to help troubleshoot process problems Methodologies/instrumentation employed include: wet chemistry, gravimetric determinations, UV/Vis Spectrophotometer, GC, ICP, X-Ray Analyzer, Auto-Titrator and SFC. This position is subject to rotating shift work, including nights, weekends and holidays. Off-shift pager responsibilities are also required. Required Skills/Experience Bachelor's Degree in Chemistry or related science field Demonstrated proficiency in laboratory environment Good oral and written communication skills Proficient in Microsoft Office Preferred Skills/Experience Two years of Refinery Laboratory experience - Required Knowledge and experience in using laboratory database systems and/or instrument operating software Good problem solving and analytical skills Familiarization with Laboratory LIMS System Understanding of refinery process flow Must have asphalt experience Job Requirements/Training Will be required to take Refinery site safety training and Drug and alcohol testing Apply now for immediate and confidential consideration or email your resume to *****************************! Benefits PTS Staffing offers a comprehensive benefits package for qualified employees which includes Medical (with employer contribution), Dental, Vision, 401k program, direct deposit PTS Advance is an Equal Opportunity Employer Pay: $30 - $31hr depending on experience

Perform environmental monitoring of cleanrooms including surface, viable air, non-viable air, and personnel monitoring (including gowning in clean rooms grade A, B,C and D, or ISO 5, ISO 7, ISO 8.). Collect water samples to ensure all sample collected per schedule and tested on time Perform and review microbiological assays such as Gram Stain, Endotoxin, Sterility, Microbial Identification, Growth Promotion, Bioburden and Plate Reading Data entry and data trend as needed. Assist in investigations regarding out of specifications (OOS) results, address and manage deviations related to micro procedures. Routine maintenance of lab equipment and lab spaces Review and approve final product release test results Coordinates waste management, LEAN and 5S efforts as required. Additional duties as assigned. These duties can be delegated to designated deputies of a satisfactory qualification level as needed.

Role: Senior Aerospace Laboratory Technician Salary: $70,000 - $100,000 Clearance: MUST be Secret cleared or higher A leading Military Aircraft Group is seeking a Senior Aerospace Laboratory Technician in Torrance, CA. This onsite role reports to the Site Engineering Lab Manager and requires an active DoD Secret Clearance. Key Qualifications: Background in mechanical, hydraulic, or electromechanical testing Experience testing to RTCA DO-160 or MIL-STD-810 (preferred) Proficiency with hand tools, test instruments, and lab equipment Familiarity with LabView, DIAdem, dSPACE, Dewesoft, or MATLAB (preferred) Responsibilities: Conduct environmental and functional tests for product development & qualification Maintain safety standards in a hazardous lab environment Set up, inspect, and operate test equipment per procedures Analyze test data, troubleshoot anomalies, and support engineers Prepare detailed test logs, reports, and documentation Provide training and collaborate across teams Benefits: Annual Profit sharing Employer matched 401k Employee stock purchase plan Health and spending saving account Comprehensive medical, dental, vision, life, disability plan Tuition assistance Growth, to achieve internal promotions This is an exciting opportunity for a highly skilled lab technician to play a key role in aerospace innovation. Apply today!

MUST HAVE EXPIERENCE WITH FARO/ROAMER ARM INPSECTION FOR CONSIDERATION Quality Inspectors oversee all inspection activities including incoming, in-process and final inspections to ensure final product meets all Company and Customer requirements. Essential Duties and Responsibilities include the following. Other duties may be assigned. Perform inspection(s) of products to determine conformance to all specifications. Utilize various measuring tools, including calipers, micrometers, gages and other hand held measuring devices for open set ups. Use an Optical Comparator for measurement of parts and characteristics. Use of portable coordinate measuring machine (CMM) Use video measurement equipment to measure part dimensions. Write programs for video measurement equipment based on parts and specification drawings. Understand and perform to all current quality standards. Prepare and update Company and Customer inspection records as required. Communicate inspection results effectively with co-workers and supervisors. Understand and use concepts like absolute position, geometric tolerance and stack-up. Use basic statistical techniques for evaluation of measurement data and trending. Have a basic understanding of machining processes to support communications of findings to the production floor. Train others on inspection techniques and tools. Work closely with engineering to determine documentation and job requirements. Accurately completes all required paperwork. Keep inspection equipment and work area clean and organized at all times. General maintenance of inspection equipment as needed. Abide by and support all safety and quality system requirements. Provide good feedback and promote good communication. Promote and live company culture. Competencies To perform the job successfully, an individual should demonstrate the following competencies: Attendance/Punctuality - Is consistently at work and on time. Dependability - Follows instructions, responds to management direction. Quality - Demonstrates accuracy and thoroughness; monitors own work to ensure quality. Safety and Security - Observes safety and security procedures; reports potentially unsafe conditions; uses equipment and materials properly. Qualifications To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Education and/or Experience High School diploma or equivalent Requires great attention to detail and the ability to read drawings and specifications Previous experience machining or programming required

Lab Technician（US） Add：Suite 150, 10 Pasteur, Irvine, CA 92618 USA Responsibilities: Perform laboratory tasks related to Next-Generation Sequencing (NGS), including but not limited to: Sample extraction (DNA extraction) Library preparation Hybridization Sequencer operation Perform laboratory tasks related to genotyping workflows, including: Sample spotting and preparation PCR amplification and optimization Fluorescence-based detection and analysis Carry out routine laboratory activities such as setup and maintenance of equipment, preparation of testing solutions, and daily cleaning and housekeeping activities. Manage inventory, including: Monitoring reagent and consumable stock levels Timely restocking and procurement to avoid disruptions Accurate tracking of stock movements, including in-stock and out-stock documentation Next-Generation Sequencing (NGS): Perform DNA extraction from various sample types with high accuracy. Prepare libraries for sequencing, including quality control and quantification. Conduct hybridization and enrichment procedures as required. Operate sequencing platforms (e.g., Illumina, BGI) and ensure data quality control. Requirements: Bachelor's degree in Biology, Genetics, Molecular Biology, or a related field. Preferred hands-on experience with NGS workflows, including library preparation and sequencing. Preferred familiarity with genotyping techniques such as PCR and fluorescence detection. Strong communication skills to effectively collaborate and convey technical information. Excellent organizational skills with attention to detail, including inventory management. Ability to multitask and work in a fast-paced laboratory environment.

As a Cleaning Employee you are responsible for carrying out cleaning activities in the cleanrooms under strict quality requirements that the pharmaceutical industry must adhere to (GMP rules). Length of contract: 6 months High school diploma Cleaning experience in a cleanroom / cGMP environment is a plus Willing to work night shifts and weekends ...

Our client, a global leader in providing tech and tools for health, science, and environmental testing is hiring a Lab Engineer to join their team in Pasadena, California! *This is a 6 month W2 contract with benefits offered! * As a Lab Engineer, you will be responsible for installing, maintaining, validating, and repairing multi-vendor instrumentation at customer sites, ensuring top-quality service. Our client is looking for someone with strong troubleshooting skills, experience repairing and providing qualification services using LCMS systems, and a background in GxP environments. Responsibilities: Install, maintain, validate, and repair multivendor instrumentation at customer sites with best-in-class service Provide scheduled and unscheduled corrective maintenance for customers including warranty services within a prescribed time frame and established maintenance protocols Provide service that helps to drive the sale of new service agreements, service agreement upgrades, and instrument add-ons to existing service contracts Requirements: Bachelor's degree in applied science, Biology, Chemistry, Electronics, Mathematics, Engineering 4+ years of experience in the ability to troubleshoot, repair, and provide qualification services in a laboratory setting 2+ years of servicing LC, LCMS systems Motion Recruitment Partners is an Equal Opportunity Employer, including disability/vets. All applicants must be currently authorized to work on a full-time basis in the country for which they are applying, and no sponsorship is currently available. Employment is subject to the successful completion of a pre-employment screening. Accommodation will be provided in all parts of the hiring process as required under Motion Recruitment Employment Accommodation policy. Applicants need to make their needs known in advance.

The Food Safety Quality Assurance (FSQA) Technician ensures the quality and safety of food products by monitoring production, enforcing GMPs (Good Manufacturing Practices), conducting quality checks, and reporting deviations from specifications. This role involves performing inspections, calibrating equipment, documenting findings, and collaborating with management to address quality and food safety issues. **Must speak conversational Spanish and currently live in the area Essential Duties & Responsibilities: Enforce GMPs, Safe Quality Food (SQF) standards, and safety regulations (including PPE) across all production areas. Ensure all employees adhere to food safety, cleanliness, and quality standards. Conduct regular GMP inspections across the facility to ensure adherence to food safety, quality, and cleanliness standards. Monitor production runs and intercede immediately when deviations from standard operating procedures occur. Inspect raw materials, in-process ingredients, and finished products to confirm compliance with specifications and quality standards. Perform pre-operational inspections to verify proper line clearance before production begins. Report deviations from product specifications, safety standards, or GMPs to the Quality Management team immediately. Identify and report unsafe conditions or potential food safety threats to management in real time. Initiate corrective actions, including placing products on hold and documenting incidents with detailed reports. Create hold tags, including a physical count and full documentation of the issue, for affected products. Calibrate thermometers, scales, and other laboratory equipment to ensure accurate measurements. Ensure that all production equipment is operating within specified parameters for quality assurance. Verify that correct formulas are used during production and ensure they are followed precisely. Monitor and ensure that production records, formulas, and lot information are accurate and up-to-date. Maintain accurate and timely documentation of inspections, calibrations, deviations, corrective actions, and quality checks. Assist with transferring paper-based documents to electronic systems, ensuring they are organized and audit-ready. Adhere to and enforce all Food Safety and Quality Standard Operating Procedures (SOPs) at all times. Report any known or suspected food safety/quality issues to management or direct supervisor. Participate in Food Safety and Quality Assurance training sessions as required. Assist in training staff on food safety protocols, GMPs, and quality standards. Qualifications: MUST have experience working in Food Manufacturing 1-2 years of experience in Quality Control in a food manufacturing facility. High school diploma or equivalent; degree in Food Science, Microbiology, or Chemistry preferred. Proficiency in Microsoft Office (Word, Excel, Access, Email). Strong understanding of GMPs, Good Laboratory Practices (GLPs), and Good Documentation Practices (GDPs). Ability to perform basic mathematical calculations (addition, subtraction, multiplication, division, ratios, and percentages). Excellent written and verbal communication skills. Detail-oriented with strong organizational and time management skills. Ability to work independently or as part of a team in a fast-paced environment. HACCP certification is preferred but not required. Fluency in English is required; bilingual (Spanish) is preferred. Physical Demands & Work Environment: Prolonged standing/walking: 90% of the time. Physical Activity: Lifting (up to 50 lbs.), climbing, crawling, pushing, and pulling (5% of the time). Hand manipulation: Frequent use of hands for typing, documentation, and equipment calibration (5% of the time). Color distinction: Ability to distinguish colors for quality control purposes. Odor tolerance: Ability to tolerate strong odors from food products during processing. Work environment: Ability to work in both hot and cold environments for extended periods. Flexible hours: Ability to work varying hours, including weekends, as needed.

As a Cleaning Employee you are responsible for carrying out cleaning activities in the cleanrooms (a ""clean"" work environment where pharmaceutical treatments are applied). Your activities therefore take place under strict quality requirements that the pharmaceutical industry must adhere to (GMP, 'Good Manufacturing Practices' rules). The Company is a biopharmaceutical company engaged in the development of innovative cancer immunotherapies. The aim is to provide fast, sustainable long-term response and remove the burden of chronic care. The Company targets the cells of the immune system that detect diseases and viruses (chimeric antigen receptor (TCR) and T cell receptor (TCR)). The Company tries to recognize, kill and strengthen these cells. In Europe, The Company recruits talent to support the development of the European region. We are building a state-of-the-art factory in Hoofddorp. We are currently looking for motivated talent for different positions to support our innovative immunotherapy for cancer. Department As a Cleaning Employee you are part of a new team in which people work together and are respected. You contribute to saving lives every day by keeping the labs as clean as possible and thus complying with the GMP requirements. You report to the Manufacturing Team Leader. The Cleaning Employee follows all procedures. He / she ensures that aseptic (sterile) and hygienic conditions are maintained and that the accompanying documentation is accurately completed. You play an important role in guaranteeing the hygienic conditions of the cleanrooms. Responsibilities include, but are not limited to: • Perform sanitary cleaning operations in a sterile environment in accordance with strict procedures and as prescribed by the supervisor • Stocking sterile and non-sterile protective garments for multiple locker rooms in the correct order • Ensuring accurate and complete documentation and signing it • Taking training courses that are required in accordance with Company's procedures and policies • Ensuring an accurate and complete inventory of cleaning products, so that sufficient stock is available • Providing assistance to other departments, if necessary • Working in a safe and effective manner in accordance with company regulations • Performing other tasks when requested.

As a Cleaning Employee you are responsible for carrying out cleaning activities in the cleanrooms (a ""clean"" work environment where pharmaceutical treatments are applied). Your activities therefore take place under strict quality requirements that the pharmaceutical industry must adhere to (GMP, 'Good Manufacturing Practices' rules). Department As a Cleaning Employee you are part of a new team in which people work together and are respected. You contribute to saving lives every day by keeping the labs as clean as possible and thus complying with the GMP requirements. You report to the Manufacturing Team Leader. The Cleaning Employee follows all procedures. He / she ensures that aseptic (sterile) and hygienic conditions are maintained, and that the accompanying documentation is accurately completed. You play an important role in guaranteeing the hygienic conditions of the cleanrooms. Responsibilities include, but are not limited to: • Perform sanitary cleaning operations in a sterile environment in accordance with strict procedures and as prescribed by the supervisor • Stocking sterile and non-sterile protective garments for multiple locker rooms in the correct order • Ensuring accurate and complete documentation and signing it • Taking training courses that are required in accordance with Kite's procedures and policies • Ensuring an accurate and complete inventory of cleaning products, so that sufficient stock is available • Providing assistance to other departments, if necessary • Working in a safe and effective manner in accordance with company regulations • Performing other tasks when requested. Your profile • Education High school diploma • Knowledge / experience Required • Following the cleanroom protocols (working according to the strict rules, regulations and procedures of Kite) • Prepare to work in a sterile environment where biological and hazardous waste is processed and disposed of on a daily basis • Able to work in a team-oriented environment • Able to read documents (prepared in English), such as standard operating procedures, operating manuals, and company and safety policies • Prepare to work at night and work overtime if necessary • Possesses a strong work ethic, reliable and punctual • Good interpersonal, verbal and written communication skills • Comfortable in a fast-changing organization • Cleaning experience in a cleanroom / cGMP environment is a plus. Personal skills • Able to work with minimal control • Flexibility to adapt to changing circumstances • Customer-oriented, result-oriented and performance-oriented • Motivated Additional requirements • Physically able, and willing to wear protective clothing and equipment, such as goggles, face shield and protective gloves • Willing to work night shifts and weekends (from mid-2020) • Living in the vicinity of Hoofddorp or in possession of your own transport because working hours make it difficult to travel by public transport

Duration: 12 months contract Responsibilities: • Monitor critical laboratory instruments and equipment to ensure compliance with qualification, maintenance and calibration schedules, initiation of service requests and escorting vendors. • Assist with coordination of set up and qualification activities for new assets. • Assist with OOT investigations in the Asset Management System. • Assist with maintenance and monitoring of stability environmental chambers, including routine visual inspection, temperature monitoring trending and coordination of cleaning and maintenance. • Assist with stability inventory and initialization activities including receiving, storage, distributing and disposal of samples for stability studies. Skills: • Strong working knowledge of cGMP, FDA and EMA GMP regulation and ICH guidance documents. • Experienced in GMP regulated drug development environment. Education and experience: • Must possess a BS in Molecular Biology, Biochemistry, or related field with at least 3+ years of relevant experience. About US Tech Solutions: US Tech Solutions is a global staff augmentation firm providing a wide range of talent on-demand and total workforce solutions. To know more about US Tech Solutions, please visit ************************ US Tech Solutions is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, colour, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran. Recruiter Details: Name: Shivangi Email: ********************************* Internal Id: 25-33847

**This is a part-time position, estimated 20 hours per week. College students welcome to apply! **To be considered for this opportunity, please apply directly at the following link: ******************************************************************************************************************************** Polytek Development Corp. is a leading manufacturer of mold making and casting materials. Polytek is currently looking for a highly motivated, experienced, and extremely organized individual to join our rapidly expanding company. Essential Job Functions: Perform QC tests on incoming raw materials as described in QC SOP. Perform QC tests on production samples as described in QC SOP. Mixing and curing test samples. Run Titrations, Viscosity measurements, Hardness measurements. Work with analytical equipment (including FTIR, TGA, rheometer, DSC). Hazardous chemical handling, storage, and disposal. Physical property testing (including viscosity, specific gravity, tensile/tear strength). Perform any testing and inspection required for customer returns. Perform any testing and inspection required for customer complaints and product non-conformance. Perform additional testing as required for off-specification raw materials and batches. Perform additional testing, ie. Soak tests, physical properties, product application, etc as directed. Interact with production personnel on pilot batches and production problems. Generate weekly QC Reports. Keep laboratory work area neat and uncluttered. Organize and maintain QC retain product samples and cured samples. Understand hazards of Polytek products through company provided training and reading SDSs and labels. Wear proper personal protective equipment (e.g., gloves and safety glasses) and follow all safety rules. Report safety concerns immediately to your supervisor. Perform other duties as assigned. Physical Demands: The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Must be able to work in a laboratory environment. Must be able to climb a ladder, frequently lift up to 8 lb, and occasionally lift up to 40 lb. Must be able to bend, squat, walk, stand, use hands to finger, handle or feel, reach with hands and arms, and repeatedly ascend/descend short flights of stairs/ladders for a full shift. Must be able to talk, hear and see with vision abilities including close/near, distance, color and peripheral vision, depth perception and ability to adjust focus. Must wear required Personal Protective Equipment (PPE) when entering laboratory or manufacturing areas. Education and Experience: Must be able to understand, speak, write, and read English. Bachelor's Degree in Chemistry or related field required. 1 - 3 years experience in quality control function in a chemical manufacturing environment is a plus. Skilled in quality processes and statistical techniques. Must have ability to work a flexible schedule, including occasional overtime. Must be proficient in Microsoft Office Suite. Must have the ability to work independently in a fast-paced environment. Strong verbal and written communication, organizational, and time management skills. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran. Important Notice: Protect Yourself from Job Application Fraud When applying for a job at Polytek, it's important to be aware of potential fraud schemes. Polytek will only contact candidates through official channels: our job portal (Paylocity) , a direct phone call from a team member, or an email from a ********************* address. We ask that all candidates apply directly to our website. We never ask candidates to make any form of payment at any point during the application process, including for interviews, background checks, or travel expenses. If you're asked for money, this is a clear indication that you may be dealing with a scam. Additionally, Polytek will never request sensitive personal information such as your Social Security number, financial details, driver's license, passport information, or birth certificate via email or phone. Any unsolicited request for this type of information should be treated as suspicious. If you believe you've been targeted by a scam or have fallen victim to identity theft, it's important to contact your local police department immediately and report the incident. You should also report any fraudulent job listings to the platform where they were posted. By staying vigilant and following these guidelines, you can protect your personal information and ensure a safe job search experience.

Must Have Basic knowledge of low and high voltage safety. Electronic Test Equipment Heavy Lifting Knowledge of mechanical drawings and Electrical schematics. Nice To Have Design of sheet metal parts and fabrication Job Summary Test setup and execution Responsibilities: Identifying and setting up test equipment for various functional system tests. Lead, implement, setup and utilize standard test equipment such as oscilloscopes power analyzers, power supplies and digital multimeters. Troubleshoot, root cause and document electronic functional failures. Perform wire harness assembly crimp and pin, soldering / de-soldering, etc. Understand how to read electrical schematics, drawings and use manufacturers' product data sheets. Fabricate special test equipment supporting development and validation testing of electronic components. Ability to use MS Word, Excel. Able to move/lift heavy boxes and fixtures. Qualification: - Technical degree or certification in electronics or related field. 3+ years of electronics technician experience. Experience using power tools, mechanical tools, fabricating special test equipment such as fixtures, test boxes and test harnesses. Experience with soldering & re-work. Experience with electrical testing and equipment (Volt Meter, CAN diagnostics,) High level of interpersonal and communication skills. Ability to work in a fast-paced development environment. Willing to work flexible hours and passionate about getting jobs done. Hands-on approach: Proactively identifies and fills in gaps where needed. Able to navigate ambiguity.

Role: Microbiology Lab Technician Duration: 6 Months The role involves performing routine laboratory testing and supporting functions in a regulated environment, including microbiology testing, environmental monitoring, and maintaining lab equipment. Key Responsibilities: Perform routine testing (sterility, bioburden, environmental collection, etc.) per established protocols. Prepare media and maintain device history records. Collect environmental samples from cleanrooms and perform data entry. Assist with testing validation and revalidation activities. Support lab inventory management, equipment calibration, and general lab housekeeping. Ensure compliance with GMP, FDA, and ISO regulations. Skills: Strong written and verbal communication. Proficient in MS Office. Knowledge of laboratory processes, QSR, FDA, ISO regulations. Attention to detail and adherence to safety protocols. Education/Experience: High school diploma or GED required; Associate's degree preferred. 0-2 years of microbiology or laboratory experience, preferably in a medical device or pharmaceutical environment. LIMS knowledge a plus.

We are seeking an experienced Lab Technician with a background in packaging or cosmetics to join our team. This role is critical to developing and ensuring the quality of innovative packaging solutions tailored to the beauty industry. Responsibilities Conduct physical, chemical, and compatibility testing of packaging materials to ensure quality standards. Use Fishbowl ERP to manage inventory, track testing materials, and maintain accurate records. Support the development and validation of new packaging designs for cosmetic products. Collaborate with cross-functional teams to assess product compatibility with packaging solutions. Accurately document all testing procedures, findings, and results. Maintain and calibrate laboratory equipment to ensure accurate testing outcomes. Follow safety standards, protocols, and industry regulations. Qualifications Degree or certification in Chemistry, Material Science, or a related field. Experience in packaging or cosmetics is required. Strong attention to detail and organizational skills. Knowledge of quality control processes and regulatory compliance within the cosmetics or packaging industry. Excellent problem-solving and communication skills. Local applicants only. Pay Range: $20/hour to $27/hr Hours: Full Time Location: Corona, California

Are you ready to bring your expert clinical skills to a world-class facility recognized as top ten in the country for cardiology? Do you have a passion for the highest quality and patient happiness? Then please respond to this dynamic opportunity available with one of the best places to work in Southern California! We would be happy to hear from you. Cedars-Sinai Medical Center has been recognized as #1 in California and eight years in a row on the “Best Hospitals” Honor Roll by U.S. News & World Report, 2023-24. The Cardiovascular Intervention Center is a core element of the Smidt Heart Institute, performing more than 8,000 procedures a year. The department serves the populations of neonates to and including geriatrics. In this twelve-laboratory facility, we perform a wide range of diagnostic and therapeutic procedures for coronary artery disease, heart muscle function and heart valve dysfunction. As a Catheterization Lab Technician, you will use physiological monitoring/recording systems to create, manipulate, improve, and record analog and digital radiographic images used in diagnostic, electrophysiology and interventional cardio-vascular procedures and examinations. You will perform a range of technical and supportive patient care tasks in accordance with facility and regulatory requirements. Experienced CVTs that meet the qualifications of Tech I and also have three years' experience along with ACLS and RCIS may qualify for the CVT Tech II position. We are currently offering a $5,000 sign-on bonus to newly hired Techs! Summary of Essential Duties: Assists with CVIC procedures applying approved protocols per standards of practice for safety, speed, organization, precision, and accuracy based upon the department's accrediting agency and/or department guidelines for exam protocols, adhering to department safety and productivity standards. Scrubs, monitors, assists, and circulates safely and timely, supplying necessary equipment and performing vascular site management, while supporting FDA approved and clinical research procedures. Performs all diagnostic tests, including coronary and structural heart intervention using electronic physiologic monitoring equipment and accurately records ECG, electrograms, hemodynamics, echocardiographic and other vital tracing obtained throughout the procedure. Prepares and administers contrast and follows department procedures and guidelines in handling of contrast to maintain compliance with all safety requirements. Observes radiation and laser protection to regulatory safety requirements. Performs sterile processing within guidelines for sterile field and equipment preparation, including inspection, counting, cleaning, patient and equipment transport, room stock, and documentation, with notification to supervisor and action needed for resolution. Sign-on bonus is available to newly hired Techs only. Current employees are not eligible. Qualifications Education: High School Diploma or GED required Successful completion of an Accredited CVT program with at least 800 hours of clinicals as part of that training program required License/Certifications: Basic Life Support from the American Heart Association or American Red Cross required ACLS preferred. ACLS is required if put into a Tech II position RCIS preferred. RCIS is required if put into a Tech II position. Experience: Previous Cath Lab experience preferred; graduates of a CV Tech program with no experience can be considered at the Tech I level At least 3 years of Cath Lab experience required to qualify for Tech II position Congenital Heart experience preferred #JOBS Keywords: Cardiac, Cardiovascular, Cath, Catheterization, Lab, Laboratory, Heart, Procedure, Tech, Technologist, Technician, Healthcare, Hospital, Medical Center, Los Angeles, CA, California About UsCedars-Sinai is a leader in providing high-quality healthcare encompassing primary care, specialized medicine and research. Since 1902, Cedars-Sinai has evolved to meet the needs of one of the most diverse regions in the nation, setting standards in quality and innovative patient care, research, teaching and community service. Today, Cedars- Sinai is known for its national leadership in transforming healthcare for the benefit of patients. Cedars-Sinai impacts the future of healthcare by developing new approaches to treatment and educating tomorrow's health professionals. Additionally, Cedars-Sinai demonstrates a commitment to the community through programs that improve the health of its most vulnerable residents. About the TeamCedars-Sinai is one of the largest nonprofit academic medical centers in the U.S., with 886 licensed beds, 2,100 physicians, 2,800 nurses and thousands of other healthcare professionals and staff. Choose this if you want to work in a fast-paced environment that offers the highest level of care to people in the Los Angeles that need our care the most. Req ID : 7308 Working Title : Cardiac Cath Lab CV Tech I - 10-Hour Day Shift - $5,000 Hiring Incentive! Department : Cardiac Cath Lab Business Entity : Cedars-Sinai Medical Center Job Category : Imaging Job Specialty : Diagnostic Imaging Overtime Status : NONEXEMPT Primary Shift : Day Shift Duration : 10 hour Base Pay : $36.31 - $56.28

As a Cleaning Employee you are responsible for carrying out cleaning activities in the cleanrooms (a ""clean"" work environment where pharmaceutical treatments are applied). Your activities therefore take place under strict quality requirements that the pharmaceutical industry must adhere to (GMP, 'Good Manufacturing Practices' rules). Responsibilities include, but are not limited to: • Perform sanitary cleaning operations in a sterile environment in accordance with strict procedures and as prescribed by the supervisor • Stocking sterile and non-sterile protective garments for multiple locker rooms in the correct order • Ensuring accurate and complete documentation and signing it • Taking training courses that are required in accordance with procedures and policies • Ensuring an accurate and complete inventory of cleaning products, so that sufficient stock is available • Providing assistance to other departments, if necessary • Working in a safe and effective manner in accordance with company regulations • Performing other tasks when requested. Your profile • Education High school diploma • Knowledge / experience Required • Following the cleanroom protocols (working according to the strict rules, regulations and procedures) • Prepare to work in a sterile environment where biological and hazardous waste is processed and disposed of on a daily basis • Able to work in a team-oriented environment • Able to read documents (prepared in English), such as standard operating procedures, operating manuals, and company and safety policies • Prepare to work at night and work overtime if necessary • Possesses a strong work ethic, reliable and punctual • Good interpersonal, verbal and written communication skills • Comfortable in a fast-changing organization • Cleaning experience in a cleanroom / cGMP environment is a plus.

As a Cleaning Employee you are responsible for carrying out cleaning activities in the cleanrooms under strict quality requirements that the pharmaceutical industry must adhere to (GMP rules). Length of contract: 6 months High school diploma Cleaning experience in a cleanroom / cGMP environment is a plus Willing to work night shifts and weekends