Quality control analyst jobs in Vacaville, CA

Performs any combination of the essential duties and responsibilities of quality control at manufacturing facility in Dixon, CA. Successful candidates will be required to participate in a pre-employment drug screen and random drug screening per our Drug Free Workplace policy. Dependability for work schedule is crucial. ESSENTIAL DUTIES AND RESPONSIBILITIES: * Inspects cast floats, float assemblies, and metal fabrications, hardware components, and lumber; * Inspects the casting process per drawing requirements; * Performs concrete tests per ACI / PCI and customer specifications; * Scans production and inspection documents; * Conducts safety tasks and inspections as required by The BMI Safety Program; and * Documents and records QC activities. * Performs other duties as assigned. 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 required. Requires knowledge of or ability to learn the characteristics of concrete float fabrication with 12 months of experience working with concrete and/or prior inspection. Requires one year of experience in Quality Control. CERTIFICATES, LICENSES, REGISTRATIONS: ACI concrete field testing tech Grade 1 Certification. Possess or ability to obtain PCI Quality Control Technician Levels 1 and 2 within 12months of hire. Ability to read production drawings. COMPUTER SKILLS: To perform this job successfully, an individual should be proficient with MS Word, MS Excel, and MS Outlook. Must be able to use a document scanner.

Details: Stefanini Group is hiring! Stefanini is looking for Microbiology Quality Control Analyst in Hayward, CA (Onsite) For quick Apply, please reach out to Sangeeta Dasadhikary - call: ********** /email: ********************************** Work Hours: M-F (40 hours) Work Location: Hayward, CA (Onsite) Shift: 1st Shift - 8:00 AM - 4:30 PM (Flexible) Conduct environmental monitoring of ISO 5, 7, 8, and 9 cleanrooms at clients manufacturing facilities along with Water collection. Support Microbiology analysis such as raw materials, in-process and finished goods products samples at manufacturing facility. Conduct Microbiological analysis on raw materials, initial, in-process and final products, and samples collected from the environmental monitoring programs at manufacturing facility. Testing as required supporting Endotoxin testing, Bioburden analysis, growth promotion, Will be required to read microbial plates and interpret test results. QC Data entry in Sample manager- LIMS Complete all testing, including special project / protocol testing in a timely and appropriate manner. Perform equipment maintenance and calibrations as required. Maintain data integrity and ensure compliance with company SOPs and specifications, FDA, GLP, QSR and cGMP regulations. Perform/or support all NCRs, CAPAs, and LIRs and be the point of contact for other departments for updates. Participate in functions involving teams, which impact production, increase efficiency, solve problems, generate cost savings, and improve quality. Perform laboratory and manufacturing audits as required. Audit and update, as required, plant/lab SOPs. Ensure Environmental Monitoring area is always maintained in a GMP state while following all EHS and 6S guidelines. Flexibility in performing other duties, as assigned, or as business needs require. Works and communicates effectively and professionally with others inside and outside the company. Weekend work may be required as needed to meet production timeline schedules. Details: B.S. degree in Microbiology, Biology; minimum 1-2-year experience in Pharmaceutical/Medical Device industry preferred. Ability to handle multiple tasks concurrently and complete tasks in a timely manner. Effective organizational skills and ability to plan and suggest resolutions to technical problems. Demonstrates some knowledge of assays/equipment in functional area. Computers literate and competent with a general knowledge of word processing and spreadsheets (such as Microsoft Office). Proficient use of laboratory equipment and tools. Must be detail[1]oriented, conscientious, and responsible. Must have effective verbal and written communication skills. Some knowledge of applicable CTP/SOPs, EHS requirements, FDA Regulations application of CGMP/GDPs. Must be able to learn about new computer systems and programs in a timely manner. Must be able to learn new computer systems and programs in a timely manner. Listed salary ranges may vary based on experience, qualifications, and local market. Also, some positions may include bonuses or other incentives. Stefanini takes pride in hiring top talent and developing relationships with our future employees. Our talent acquisition teams will never make an offer of employment without having a phone conversation with you. Those face-to-face conversations will involve a description of the job for which you have applied. We also speak with you about the process including interviews and job offers. About Stefanini Group The Stefanini Group is a global provider of offshore, onshore, and near shore outsourcing, IT digital consulting, systems integration, application, and strategic staffing services to Fortune 1000 enterprises around the world. Our presence is in countries like the Americas, Europe, Africa, and Asia, and more than four hundred clients across a broad spectrum of markets, including financial services, manufacturing, telecommunications, chemical services, technology, public sector, and utilities. Stefanini is a CMM level 5, IT consulting company with a global presence. We are CMM Level 5 company. #LI-SD2 #LI-ONSITE

Full-time Description Summary: Harbinger Production, Inc is an innovative manufacturing company specializing in industrialized, stick-framed multi-family housing. We utilize advanced techniques to streamline construction processes, reduce costs, and prioritize sustainability. As an Equal Opportunity Employer, we value diversity and promote a collaborative work environment. We are seeking a detail-oriented and technically skilled QC Assistant to support Harbinger Production's quality control team by conducting inspections, recording findings, and assisting with defect detection and correction. This role also includes progress photography responsibilities to document key construction stages, supporting quality verification and continuous improvement. Responsibilities: Inspection & Quality Support Assist in daily inspections of modular units at all production stages, verifying compliance with the International Building Code (IBC), state/local regulations, and Harbinger's design specifications Perform basic functional tests on HVAC, electrical, and plumbing systems under supervision Record inspection findings, non-conformance reports, and rework logs using digital tools (Bluebeam Revu, Excel) Participate in root-cause analysis and support implementation of corrective actions Support material checks for proper storage, handling, and sequencing of construction components Documentation & Reporting Organize and maintain quality records, including inspection logs, non-conformance reports, and summary reports for senior QC staff Track recurring defects and contribute to lean manufacturing initiatives aimed at reducing waste and improving quality Provide logistical support during third-party inspections, audits, and client walkthroughs Progress Photography & Visual Documentation Capture high-resolution photographs of structural elements, MEP (mechanical, electrical, plumbing) systems, and waterproofing installations prior to enclosure or concealment Document daily production milestones and quality checkpoints to validate schedule adherence and task completion Work closely with QC team members to identify critical documentation points and provide photographic evidence for detected quality issues Maintain an organized digital photo library with systematic naming, metadata tagging, and secure backup Prepare concise visual reports to aid issue detection, dispute prevention, and stakeholder communication Team Collaboration & Communication Coordinate with production teams to schedule inspections and photography without disrupting workflow Attend quality meetings to share inspection findings and photographic documentation Communicate minor defects and verification of corrective actions clearly to production personnel Requirements Education & Experience Associate's degree in Construction Management, Photography, or related field preferred 2-5 years of experience in construction quality control or progress documentation Technical Skills Proficiency with digital photography (DSLR/mirrorless cameras), lighting, and photo-editing software (Lightroom, Photoshop) Familiarity with digital asset management systems and metadata tagging Experience using Bluebeam Revu, Excel, and Revit or similar software to interpret design specifications Construction Knowledge & Certifications Strong understanding of the International Building Code (IBC) and applicable state/local building standards OSHA 10-Hour Certification required; knowledge of construction site safety protocols and PPE Basic knowledge of MEP systems and building envelope components Personal Attributes Excellent attention to detail and organizational abilities Strong verbal and written communication skills Ability to multitask, prioritize, and work independently in a fast-paced manufacturing setting Physical capability for standing, walking, and occasional lifting within a manufacturing environment Working Conditions Standard business hours with flexibility for critical production milestones and occasional overtime Onsite work in a manufacturing facility with required PPE and strict adherence to safety protocols Harbinger Production, Inc is an Equal Opportunity Employer and Prohibits Discrimination and Harassment of Any Kind. All employment decisions at Harbinger Production, Inc are based on business needs, job requirements, and individual qualifications, without regard to race, color, religion, national origin, sex, age, physical or mental disability, HIV status, sexual orientation, gender identity and/or expression, marital, civil union, or domestic partnership status, past or present military service, family medical history or genetic information, family or parental status, or any other status protected by the laws or regulations in the locations where we operate. Harbinger Production, Inc will not tolerate discrimination or harassment based on any of these characteristics. Salary Description $60k-$70k, DOE

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 our website ********************************** are constantly on the lookout for professionals to fulfill the staffing needs of our clients, and we currently have a job opening that may interest you Title: Quality Control Analyst Duration: 12 Months Location: Berkeley, CA 94710 Job Description: Biological Development Assay Development, Quality Control (BD AD-QC) Position summary: The purpose of this position is to support analytical testing for a wide variety of methods to reach department timelines Position duties & responsibilities: The candidate will perform routine Clinical and Development testing activities with expertise in a wide variety of methods ranging from Chemistry to Biochemistry involving, but not limited to, HPLC, ELISA,qPCR, A280, Western Blot, PAGE, Protein Concentration, Osmolality, etc. Additionally, candidate will review data generated by other analysts on these, as well as other methods, with appropriate training. Must be able to follow Standard Operating Procedures (SOPs) in performance of laboratory testing to complete assigned tasks to meet release timelines and ensure quality. Must be able to document test results accurately and legibly to meet regulatory requirements and ensure completeness and accuracy per cGMPs and/or cGLPs. Must be able to compile and enter data into LIMS, Excel, or other application as needed, to be used for tracking and trending purposes. Experience using ChemStation, SoftMaxPro, and OpenLAB a plus. Qualifications Requirements/Preferences Education Requirement(s): BS/BA Ideal candidate will have 2+ years of experience in a cGMP laboratory environment with demonstrated ability to learn new skills to achieve proficiency. Thanks & Regards, Mayank Gupta, (M. Pharmacy) (Lead Pharma Technical Recruiter) 10 Exchange Place, Suite 1710, Jersey City, NJ 07302 Whats app: ************** Twitter: @mayankpharma Additional Information All your information will be kept confidential according to EEO guidelines.

Genefab is seeking an experienced analyst to join it's Quality Control Analytical group. In this role, you will support the GMP QC testing at GeneFab, with a focus on testing, method transfer, qualification, troubleshooting and investigations.Responsibilities Provide technical expertise (SME). Provide technical support to Analytical Development and QC Analytical Operations as needed. Develop, implement, and update all Quality Control SOPs, testing records and other documentation needed for cGMP compliance. Perform QC testing on in-process and final product samples to support release and stability testing. Lead and perform technical root-cause investigations for aberrant results and deviations relating to analytical methods. Lead and train junior employees to ensure testing procedures and practices comply with all applicable regulations and procedures. Plan, lead, and execute analytical method transfers, qualifications, and validations. Draft, Review, and Approve Method Transfer Protocols and Reports Generate and review procedures, protocols and reports. Proactively identify areas for continuous improvement in processes and procedures and lead these initiatives. Collaborate closely with Interdepartmental MSAT, ASAT, and Manufacturing groups to support, execute, and/or provide oversight in the execution of method optimization, characterization, troubleshooting, transfer, and qualification Perform additional duties as assigned Requirements B.S. degree in biology or related field with experience in cell therapy, immunology, cancer biology, or a closely related field. Minimum of 5+ years of GMP/QC Laboratory experience. Demonstrated ability to collaborate and work in cross-functional teams. Strong organizational skills and attention to detail Strong time management skills with a proven ability to meet deadlines Strong analytical and problem-solving skills Experience with relevant technologies such as: multicolor flow cytometry, cell culture (e.g., aseptic techniques, cell line expansion), multiplexed immunoassay, qPCR, and dPCR methods, Luminex, and ELISA. Experience in GMP. Experience with contract laboratories and or CDMO is a plus Knowledge related to laboratory information management systems (LIMS) and electronic lab notebook record keeping (ELN) is a plus Proficient in MS Word, Excel, Project, and PowerPoint Experience with cell therapy or gene therapy is a plus Availability to work extended hours such as evenings or weekends to meet deadlines when necessary Comfortable in a fast-paced environment with minimal direction and able to adjust workload based on changing priorities Self-motivated, detail-oriented, and willing to accept temporary responsibilities outside of the initial job description Able to lift up to 40 pounds $45 - $55 an hour About GeneFab GeneFab is a contract manufacturing and synthetic biology biofoundry focused on cell and gene therapies. GeneFab was formed in 2023 with a vision to combine industry leading expertise in synthetic biology with advanced cGMP capabilities in order to accelerate the development and commercialization of genetic medicines. GeneFab offers its customers an extensive technology platform and know-how that spans early stage product design, technical development, and cGMP compliant production. GeneFab's technology platform includes bioinformatic-guided discovery of cell type promoters, directed evolution of small molecule-regulated gene switches, and the engineering of highly sensitive kill switches for enhanced safety and control of cellular therapies. We are committed to an inclusive and diverse GeneFab. We believe that different perspectives lead to better ideas, and better ideas allow us to better understand the needs and interests of our diverse GeneFab team. We welcome people of different backgrounds, experiences, abilities, and perspectives and are an equal opportunity employer.We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.

Axolabs is a business unit of LGC, and a leading provider of CRO / CDMO capability to the therapeutic oligonucleotide discovery and development industry. Centred out of LGC's site in Kulmbach, Germany, Axolabs works closely with its customers to assist the identification and development of lead candidates with a broad suite of bioinformatics, biology, chemistry, manufacturing and analytical services that support discovery, pre-clinical and clinical trials and scale-up manufacture. With a track record in Nucleic Acid Therapeutics that traces back more than 20 years, Axolabs provides deep knowledge and expertise in the services it provides, working collaboratively and responsively with its clients to assist them in achieving their objectives. Axolabs facility in Petaluma is focused on manufacturing scale-up and production to cGMP of multigram to kilograms of API for pre-clinical and clinical development. Our site in California has been involved in oligonucleotide synthesis for three decades and established the therapeutics activity in 2019. With around 70 staff and two manufacturing trains, Axolabs offers a flexible manufacturing service out of Petaluma that draws where necessary on our industry and chemical and analytical expertise in Kulmbach. Job Description This is an Swing Shift: Monday-Thursday (4 x 10 hours, 1pm - 11:30pm). The QC Associate Scientist brings scientific experience to LGC and is open to both learning more and sharing knowledge with others. You will be part of an ambitious and collaborative team that strives for flawless execution in all tasks. Setting up instrument sequences, while monitoring analysis and data Performing instrument troubleshooting, maintenance, and reporting of results for timely delivery to internal and external collaborators Coordinating routine and stability analysis, while driving continuous improvement via analytical methodologies Maintaining appropriate quality control processes and procedures to determine accuracy and precision of analysis Demonstrating a familiarity with GMP guidelines 21 CFR Part 210/211 and ICHQ7 Qualifications Minimum Qualifications: Science degree in Chemistry, Biology or similar with 2 years lab experience in manufacturing Must have strong organic chemistry and/or analytical chemistry knowledge, and proficiency in associated analytical techniques; HPLC, LC-MSMS or GC-MS Proficient in cGMP Solid understanding of analytical manufacturing support Preferred Qualifications: Experience in size exclusion, ion exchange, and reverse phase chromatography, KF, FT-IR and NMR techniques preferred Additional Information What we offer (US based-employees): Competitive compensation with strong bonus program Comprehensive medical, dental, and vision benefits for employees and dependents FSA/HSA Pre-tax savings plans for health care, childcare, and elder care Deductible Buffer Insurance and Critical Illness Insurance 401(k) retirement plan with matching employer contribution Company-paid short- and long- term disability, life insurance, and employee assistance program Pet Insurance for our furry friends Enhanced Parental leave of 8 additional weeks PTO that begins immediately Town Hall monthly meeting onsite/virtual, Cheer program where employees are recognized for outstanding work, Company wide social events and much more! The typical pay range for this role is: Minimum: $ 28.12 /Hourly Maximum: $ 43.19 /Hourly This range represents the low and high end of the anticipated salary range for the California -based position. The actual base salary will depend on several factors such as: experience, skills, and location. ABOUT LGC: LGC is a leading, global life science tools company, providing mission-critical components and solutions into high-growth application areas across the human healthcare and applied market segments. Its high-quality product portfolio is comprised of mission-critical tools for genomic analysis and for quality assurance applications, which are typically embedded and recurring within our customers' products and workflows and are valued for their performance, quality, and range. OUR VALUES PASSION CURIOSITY INTEGRITY BRILLIANCE RESPECT EQUAL OPPORTUNITIES LGC strongly believes that every job applicant and employee should be valued for their individual talents regardless of age, disability, race, color, ethnic or national origin, sex, sexual orientation, gender reassignment, marital or civil partnership, pregnancy or maternity, religion, or belief. Short listing, interviewing and selection will always be carried out without regard to gender, sexual orientation, marital status, color, race, nationality, ethnic or national origins, religion or belief, age, or trade union membership. For more information about LGC, please visit our website **************** #scienceforasaferworld

QC/QA Technician - Job Description The QC/QA Technician is responsible for ensuring that products meet company quality standards and regulatory requirements throughout all stages of production. This role performs routine inspections, testing, documentation, and verification activities to support consistent product safety, quality, and compliance. Key Responsibilities Conduct quality checks on raw materials, in-process products, and finished goods to ensure they meet established specifications. Perform routine line inspections-including temperature monitoring, labeling verification, seal integrity, weight checks, and coding accuracy. Collect, record, and maintain accurate quality data in accordance with company, customer, and regulatory guidelines. Monitor GMPs (Good Manufacturing Practices) across production areas and report deviations or non-conformances promptly. Assist with root-cause investigations, corrective actions, and continuous improvement initiatives. Calibrate, operate, and maintain laboratory or quality testing equipment as required. Collaborate with production, sanitation, and management teams to support a safe and compliant manufacturing environment. Ensure adherence to food safety, quality policies, and regulatory standards such as FDA, USDA, HACCP, or SQF (as applicable). You should be proficient in: Food Safety and Quality Assurance (FSQA) Basic Computer Skills

This is where your work makes a difference. At Baxter, we believe every person-regardless of who they are or where they are from-deserves a chance to live a healthy life. It was our founding belief in 1931 and continues to be our guiding principle. We are redefining healthcare delivery to make a greater impact today, tomorrow, and beyond. Our Baxter colleagues are united by our Mission to Save and Sustain Lives. Together, our community is driven by a culture of courage, trust, and collaboration. Every individual is empowered to take ownership and make a meaningful impact. We strive for efficient and effective operations, and we hold each other accountable for delivering exceptional results. Here, you will find more than just a job-you will find purpose and pride. Your Role at Baxter The Manufacturing Technician IV is responsible for assisting the supervisor in organizing, scheduling and directing other team members as well as execute all processes in production while strictly adhering to cGMP, environmental health and safety guidelines and any other related regulations which could apply. Manufacturing Technician IV may be the main interface with other functional departments to resolve issues. Represent the department in cross- functional team as necessary. Your team: Baxter is focused on saving and sustaining lives by manufacturing high-quality products. We strive to create quality products for our customers each day. Delivering life-saving products is about getting them right, and attention to detail is how we make sure we meet that challenge. We are a team that supports each other throughout each shift. Working together in a supportive and open culture makes our processes evolve for the better and engages our workforce. What You'll Be Doing In-depth process knowledge of related manufacturing techniques and specialties. Perform and lead local manufacturing operations. Set up and operate general production equipment. Perform complex equipment troubleshooting and respond to process alarms as necessary. Support supervisor in reviewing relevant paperwork following GDP/GMP guidelines. Initiation and lead Continuous Improvement Teams. Receive and distribute supplies into the production area as necessary. Create and revise pertinent documentation as appropriate. Lead stretching exercises. Prepare and package product for shipment, where applicable. Train and mentor other team members and monitor training for newer team members. Collaborate with all other functional groups to ensure preventative maintenance is scheduled and completed. Print out and reconcile proper process documentation. Complete and closed GME and Maximo work orders Perform and lead cycle count and variance investigations. May perform other duties as assigned. What You'll Bring Requires High School diploma or GED equivalent with a minimum of 5-6 years of manufacturing related experience or AA degree with 3-4 years of manufacturing related experience required or Bachelor's degree with a minimum of 1 year of manufacturing related experience Must be proficient in written and verbal communication skills and understanding of cGMP regulations. Incumbent must be proficient in a variety of mathematical disciplines and be able to work with both the metric and USA standards of measurement. Must be able to read and follow detailed written instructions. Good interpersonal skills and be able to work effectively and efficiently in a team environment. This position requires shift, weekend and holiday work. Overtime may be required at times. The incumbent must work in a clean room/classified environment wearing special garments. Additionally, personal protective equipment and hand sanitizer must be worn due to safety requirements. Advanced knowledge of Microsoft Office/Word/Excel applications. We understand compensation is an important factor as you consider the next step in your career. At Baxter, we are committed to equitable pay for all employees, and we strive to be more transparent with our pay practices. The estimated base salary for this position is $60,000 - $82,500 annually. The estimated range is meant to reflect an anticipated salary range for the position. We may pay more or less than of the anticipated range based upon market data and other factors, all of which are subject to change. Individual pay is based on upon location, skills and expertise, experience, and other relevant factors. This position may also be eligible for discretionary bonuses. For questions about this, our pay philosophy, and available benefits, please speak to the recruiter if you decide to apply and are selected for an interview. US Benefits at Baxter (except for Puerto Rico) This is where your well-being matters. Baxter offers comprehensive compensation and benefits packages for eligible roles. Our health and well-being benefits include medical and dental coverage that start on day one, as well as insurance coverage for basic life, accident, short-term and long-term disability, and business travel accident insurance. Financial and retirement benefits include the Employee Stock Purchase Plan (ESPP), with the ability to purchase company stock at a discount, and the 401(k) Retirement Savings Plan (RSP), with options for employee contributions and company matching. We also offer Flexible Spending Accounts, educational assistance programs, and time-off benefits such as paid holidays, paid time off ranging from 20 to 35 days based on length of service, family and medical leaves of absence, and paid parental leave. Additional benefits include commuting benefits, the Employee Discount Program, the Employee Assistance Program (EAP), and childcare benefits. Join us and enjoy the competitive compensation and benefits we offer to our employees. For additional information regarding Baxter US Benefits, please speak with your recruiter or visit our Benefits site: Benefits | Baxter Equal Employment Opportunity Baxter is an equal opportunity employer. Baxter evaluates qualified applicants without regard to race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, protected veteran status, disability/handicap status or any other legally protected characteristic. Know Your Rights: Workplace Discrimination is Illegal Reasonable Accommodations Baxter is committed to working with and providing reasonable accommodations to individuals with disabilities globally. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please click on the link here and let us know the nature of your request along with your contact information. Recruitment Fraud Notice Baxter has discovered incidents of employment scams, where fraudulent parties pose as Baxter employees, recruiters, or other agents, and engage with online job seekers in an attempt to steal personal and/or financial information. To learn how you can protect yourself, review our Recruitment Fraud Notice.

**Job Title: Machine Operator** We are seeking a skilled Machine Operator to join our dynamic team. You will be responsible for the setup, sanitation, operation, and routine maintenance of capsulation machines, ensuring the production meets quality and safety standards. **Responsibilities** + Perform setup, sanitation, operation, and maintenance of capsulation machines. + Clean machines, equipment, and work areas using appropriate cleaning aids. + Ensure capsulation machines and areas are sanitary and report any issues to a supervisor. + Read work orders and Master Manufacturing Record to determine production specifications. + Pour, scoop, or dump specified mixtures into machines as per production requirements. + Adjust machine components to regulate speeds, pressures, temperatures, and material flow. + Perform test runs and examine sample capsules to ensure conformance to specifications. + Clean, oil, and make minor adjustments or repairs to machinery as needed. + Record production data including meter readings, quantities, and capsule specifications. + Transfer completed capsules to drying or storage areas, ensuring they are covered at all times. + Conduct ongoing assessment of quality control and operational procedures. + Meet or exceed production goals and guidelines. **Essential Skills** + High school diploma or equivalent with one to two years of related experience. + Strong organizational, problem-solving, and analytical skills. + Knowledge of production processes and quality control techniques. + Understanding of machine and tool designs, uses, repair, and maintenance. + Strong mechanical aptitude. + Good judgment with the ability to make timely and sound decisions. + Ability to follow written and verbal instructions and safety requirements. **Additional Skills & Qualifications** + Versatility and flexibility in adapting to changing priorities. + Ability to perform physical labor, including walking, kneeling, bending, standing, and lifting up to 50 pounds. + Ability to operate hand trucks, forklifts, and pallet jacks if required. **Why Work Here?** Join a team that values excellence and high standards. We offer a supportive work culture where your contributions are recognized. Our dynamic environment encourages growth and development, providing opportunities to enhance your skills and advance your career. **Work Environment** Work in a warehouse environment where temperatures can be cool to hot, and noise levels may vary from moderate to high. You will be required to wear protective gear such as gloves, face masks, and uniforms. The role involves exposure to small particles and odors. **Job Type & Location** This is a Contract position based out of Livermore, CA. **Pay and Benefits** The pay range for this position is $20.00 - $27.00/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: - Medical, dental & vision - Critical Illness, Accident, and Hospital - 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available - Life Insurance (Voluntary Life & AD&D for the employee and dependents) - Short and long-term disability - Health Spending Account (HSA) - Transportation benefits - Employee Assistance Program - Time Off/Leave (PTO, Vacation or Sick Leave) **Workplace Type** This is a fully onsite position in Livermore,CA. **Application Deadline** This position is anticipated to close on Dec 3, 2025. **About Aerotek:** We know that finding work is hard, and finding meaningful work is harder. Aerotek connects 180,000+ light industrial and skilled trades workers with 14,000+ employers each year, helping our workers navigate an evolving labor market and find jobs that meets their goals, skills and interests. Since 1983, we have provided a variety of career opportunities across North American industry - from short-term assignments at Fortune 500 companies where you can build your skills, to long-term opportunities where you can play a vital role solving for companies' construction, manufacturing and maintenance challenges. Our 1,500+ experienced recruiters across 250+ offices work relentlessly to put our workforce in a position to thrive. Let us rise to meet your challenges and put our people-are everything spirit to the test as your career continues to grow. Aerotek offers weekly pay, employee benefits including medical, dental & vision, life insurance, health advocacy and employee assistance programs, a 401(k) plan, and employee discounts. The company is an equal opportunity employer and will consider all applications without regards to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

* Ability to manage Quality on multiple projects * Supervise Quality staff * Train Quality activities and requirements at a divisional level * Assist Division Quality Manager as directed * Lead project team through engagement and processes * Ability to work with and report to senior management * Develop understanding/working knowledge of corporate quality control program, company standards, procedures, and building codes, required to perform assigned work * Develop Water+Min5 plan with project team * Review, comment, and work through Division Quality Manager for approval of trade partner project specific Quality Control Plans * Perform inspections and witness tests applicable to discipline to determine acceptability of work * Maintain work performance records, inspection records and other related items; assure correctness of all documents * Work with Project Manager and Site Superintendent to manage site quality program and assist in providing solutions to non-compliant items * Assist in preparation/implementation of quality control program, including but not limited to; procedures, inspection instructions, the control of measurement and testing equipment * Participate in internal/external quality control audits * Assist in reviewing purchase and submittal documents to ensure compliance with quality control requirements * Assist in resolution of reported project non-conformance issues * Monitor subcontractor work to ensure compliance with company standards, procedures and codes, when applicable * Ensure timely and successful implementation of corrective measures * Assist in and document commissioning processes * Complete other responsibilities as assigned Physical Demands and Environmental Conditions: * Occasional exposure to dust and fumes * Requires frequent stooping/bending/crouching, reaching, handling, finger dexterity, sitting, standing, walking, and lifting 20 or more lbs * Constant finger dexterity and ability to hear, and talk, and possess depth perception * Occasional climbing and carrying * The noise intensity level is moderate SUMMARY OF BENEFITS: This role is eligible for the following benefits: medical, dental, vision, 401(k) with company matching, Employee Stock Ownership Program (ESOP), individual stock ownership, paid vacation, paid sick leave, paid holidays, bereavement leave, employee assistance program, pre-tax flexible spending accounts, basic term life insurance and AD&D, business travel accident insurance, short and long term disability, financial wellness coaching, educational assistance, Care.com membership, ClassPass fitness membership, and DashPass delivery membership. Voluntary benefits include additional term life insurance, long term care insurance, critical illness and accidental injury insurance, pet insurance, legal plan, identity theft protection, and other voluntary benefit options. If you like wild growth and working with happy, enthusiastic over-achievers, you'll enjoy your career with us!

We are SGS - the world's leading testing, inspection and certification company. We are recognized as the global benchmark for sustainability, quality and integrity. Our 99,600 employees operate a network of 2,600 offices and laboratories, working together to enable a better, safer and more interconnected world. Our Hayward, CA laboratory is looking for an experienced laboratory analyst to join their team! The Lab Analyst will prepare and analyze samples with accuracy and precision in accordance to SGS' analytical SOPs. The Lab Analyst works independently and as part of a team to meet daily production targets and ensure turnaround times are met. The Lab Analyst understands and applies basic science principles. The Lab Analyst always follows safe laboratory practices and maintains a safe working environment. Job Functions After appropriate training independently prepares and analyzes samples according to SGS' analytical SOPs using instrumentation specific to the department and analytical methodologies Performs routine operation, maintenance, calibration of laboratory instruments/equipment Preparation and analysis of bulk and solid materials for asbestos content using PLM (Polarized Light Microscopy). Determination of visual percentage and optical properties of asbestos and non-asbestos material. Preparation and analysis of air, wipe, and bulk samples for metals analaysis. Entering sample data, analysis data and preparing reports on LIMS system Inputs and maintains technical information as needed to support the laboratory functions/operations. Adheres to internal standards, policies and procedures. Performs other duties as assigned. Work Schedule Monday - Friday 8 - 5 Occasional Overtime Qualifications Associate Degree in a Chemistry or similar scientific discipline and 3-5 years of years' relevant experience in Analytical Chemistry Laboratories (Required) Bachelor's Degree in a Chemistry or similar scientific discipline and 5+ years of years' relevant experience in Analytical Chemistry Laboratories (Preferred) Advanced English language skills (Required) Strong mathematical and reasoning skills (Required) Proficiency in Microsoft Office programs (Required) Ability to lift, carry, push, and/or pull upwards of 25 lbs on a frequent basis (Required) This position pays $26 - $28 per hour (dependent on experience) and is eligible for overtime pay. In addition, your compensation package includes the following benefits: Participation in the Company's benefit programs coincident or following the first of the month in which you are hired. Immediate eligibility to participate in the Company's 401K Retirement Plan Paid vacation Four (4) floating holidays annually Seven (7) company observed holidays paid Sick time accrual Additional Information SGS is an Equal Opportunity Employer, and as such we recruit, hire, train, and promote persons in all job classifications without regard to race, color, religion, sex, national origin, disability, age, marital status, sexual orientation, gender identity or expression, genetics, status as a protected veteran, or any other characteristics protected by law. To perform this job successfully, an individual must be able to perform each essential duty satisfactorily with or without reasonable accommodations. The requirements listed above are representative of the knowledge, skills, and/or abilities required. This job description should not be construed as an exhaustive statement of duties, responsibilities or requirements, but a general description of the job. Nothing contained herein restricts the company's rights to assign or reassign duties and responsibilities to this job at any time. If you are applying for a position within the United States and you have difficulty completing the on-line employment application because of a disability, please call ************ for assistance and leave a message. You will receive a call back. Please note, this phone number is not for general employment information, but is only for individuals who are experiencing difficulty applying for a position due to a disability.

Job DescriptionSalary: $23.00 - $25.00 per hour DOE Ideal Candidate Profile Do you fit this profile? Wants to start a CAREER / not just another "job" Wants to make a difference High Moral Standards & Values Positive Helpful Team Player Professional Wants to be the best of the best Is Ready Envirocheck is a growing company and has exciting opportunities for A players on our team. Job Summary Analysis of environmental samples for asbestos fibers, fungal spores, bacteria, and lead (Pb). Applicable equipment includes: A variety of microscopes, including Compound, Stereo, PLM (Polarized Light), and PCM (Phase Contrast). Flame Atomic Absorption Spectrometer IDEXX Colisure, Colilert, and Enterolert Microbiological media Requirements Bachelor's Degree in Biology, Microbiology, Geology, or related science Preferred Experience (not required, will train) Asbestos Analysis by PLM Fiber Analysis by PCM ISO 17025 Microscopes Excel programming is a plus Knowledge of construction (building) materials is a plus Benefits Health Insurance 401K with matching Paid sick / Vacation & Personal Time Paid Company Holidays

The Quality Control Inspector is responsible for maintaining quality standards by inspecting and approving machined, in-process production, purchased and finished products; recording quality results. The QC Inspector will work under limited supervision and directly with other inspectors and machinists to deliver a high quality product. Essential Duties & Functions: Completes all duties and responsibilities in adherence with Tri Tool's core values. Perform manual inspection of parts on surface plate using mechanical hand tools such as height gages, micrometers, and calipers. Inspects first article, in-process and final products by confirming product meets applicable drawings and specifications; conducting visual and measurement tests; documenting and communicating rejections of unacceptable items. Inspection of products for outside processes such as: heat treat, machining, plating/painting, engraving etc. Receiving inspection of purchased products and outside processes. Operate Manual and DCC bridge CMMs running CMM Manager. Write programs, fixture, and report for machined metal parts. Record and document inspection data in logs and computer tracking tools. Keep inspection and measurement equipment operating by following operating instructions; and notifying management when repairs are deemed necessary. Perform in-house calibrations on equipment such as micrometers, plug gages, thread gages, etc. Maintains a safe and healthy work environment by following standards and procedures; complying with State, Federal, and Company safety regulations. Effectively communicates with coworkers and managers to support efficient production. Performs other work in related duties as assigned to ensure a highly maintained and safe department. Work as part of the team to ensure productivity and cross train to other departments as needed. Requirements Requirements & Qualifications: High School Diploma or equivalent. A.A. degree in Machining/Inspection desirable; 2+ years of experience in field machining or manufacturing or technical training related to manufacturing; 1-2 years of full time inspection experience with previous machining experience. May consider machining experience only with directly related technical training; Proficient with inspecting multiple production processes including; turning, milling, grinding, fabricating, etc.; Ability to demonstrate a high level in reading and interpreting blueprints, specifications, and related documents; Familiar with ansi y14.5; Knowledge of ISO practices. Calculate figures using basic shop math; Reading of calipers, micrometers, bore gages, dial indicators, height gages, etc.; Operate manual and DCC CMM; Working knowledge of Tri Tool's product line preferred; Basic computer skills; MS Office applications and/or Inspection Software; Must have and demonstrate good decision making skills. Salary Description $25-$28 per hour depending on experience

Working in collaborative group environment, we manufacture high quality custom oligonucleotides in a high efficiency, fast paced setting. These oligos manufactured are used in a variety of applications including helping perform genetic research, diagnose disease and help with food supply. What will you do? You work with a team to Manufacture Custom Oligonucleotides for use in the biotech industry by following established protocols and SOPs. The team uses semi-automated and automated basic lab equipment. Regularly evaluate non-routine test results and either fail the product or allow it to continue through the production cycle. Highly repetitive tasks for prolonged periods of time. Understand scientific principles in order to problem solve, troubleshoot test results, evaluate alternative choices and exercise independent judgment in selecting the best solution. Provide multiple decision options and corresponding logic/data behind the decisions. Proactively identifies production problems. Provides input and shares ideas and suggestions about improving lab techniques, protocols, processes, special handling of the product and equipment. Balance multiple tasks. Demonstrate knowledge in the use of basic lab techniques and basic computer knowledge. Demonstrate ability to meet standards as defined by the manufacturing process. Thoroughly and accurately complete documentation (completion of Batch Records, document data verifications, document problems, bring deviations to the attention of the Supervisor/Manager). Continuously strive to improve output goals. Demonstrate good time management resulting in efficiency. Support cost improvement initiatives by reducing failures, improving capacity and using supplies wisely. Reduce work in process, queues and cycle times. Advise appropriate people about problems/questions; be prepared to discuss problems/questions clearly. May be required to perform other related duties as required and/or assigned. Position occupies a significant role in mainstream oligonucleotide production. The role requires the ability to exercise judgment within generally defined practices and policies in selecting methods and techniques for obtaining solutions. Skills Chemistry, Formulation, Gmp Top Skills Details Chemistry,Formulation,Gmp Additional Skills & Qualifications * Degree in the bench sciences (Biology, Chemistry, etc) is preferred but a HS diploma can be considered. * Strong digital literacy including familiarity with relevant software (Excel and Word) are required. * 1 year of lab experience preferred (1 year maybe acquired through work or school). * Proven track record of working well with others in a collaborative team environment. Knowledge, Skills, Abilities: * Operate in a fast-paced environment and while working as a team. * Efficient worker whom can multitask across multiple areas within the manufacturing environment. * Required to be able lift up to 20 lbs * Ability to stand while performing duties. * Capable of working safely with chemicals and hazardous materials. * Capacity to work outside of regular work hours when business demands call for it. Experience Level Intermediate Leve Job Type & Location This is a Contract position based out of Pleasanton, CA. Pay and Benefits The pay range for this position is $25.45 - $25.45/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: * Medical, dental & vision * Critical Illness, Accident, and Hospital * 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available * Life Insurance (Voluntary Life & AD&D for the employee and dependents) * Short and long-term disability * Health Spending Account (HSA) * Transportation benefits * Employee Assistance Program * Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in Pleasanton,CA. Application Deadline This position is anticipated to close on Dec 8, 2025. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Work Schedule Third Shift (Nights) Environmental Conditions Able to lift 40 lbs. without assistance, Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Cleanroom: no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair etc... allowed, Loud Noises (Equipment/Machinery), Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.), Standing for full shift, Will work with hazardous/toxic materials Job Description Formulation Technician II 1st Shift: 6a-2:30pm PST Starting around $24/hr.! As part of the Thermo Fisher Scientific team, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day 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, making sure our food is safe or helping find cures for cancer. Location/Division Specific Information: The position is available at our Pleasanton site in California supporting the Genetic Sciences Division. How Will You Make an Impact?: The Pleasanton site is seeking a Formulation Technician II with interest in life sciences and biotechnology. The candidate will part of a manufacturing team for oligonucleotides and related products such as assays, arrays, and kits. A Day in the Life: Manufacture products as delegated by the Production Team Supervisor or Team Leader: Complete lab operations e.g. with automated systems like DNA/RNA synthesizers, liquid handlers, and with analytical instrumentation like HPLC and LCMS. Report metrics to the team leader during daily Tier Meetings and address and report any problems in and propose effective countermeasures. Education: High school diploma or equivalent required. Experience: Required: Minimum of 1 year of work experience in a manufacturing, operations, production, lab setting or related field Preferred: Experience in a cGMP environment Knowledge, Skills, Abilities: Follow written SOPs and batch records and revise as needed. Perform manufacturing/ production tasks as scheduled. Handle and work with biological and chemical reagents. Maintains quality service by established organization standards. Ability to coordinate and prioritize work to ensure timely delivery. Communicate effectively with other production staff. Achieve high efficiency by reliable and punctual attendance. Physical Requirements / Work Environment Specific gowning is required including gloves, safety glasses with no makeup / jewelry, and hair, beard net and face cover for some operations. Ability to infrequently lift and manipulate up to 40 pounds unassisted. Ability to stand and move about including reaching, bending, stooping, grasping. Ability to use hand tools and equipment including forceful gripping, grasping, pushing, pulling and repetitive motion. Ability to use PPE (Personal Protective Equipment) and understand chemical hygiene including labels and SDS (Safety Data Sheets), common chemicals are disinfectant, solvents and IPA (Isopropyl Alcohol 70% and 99%). What We Offer Compensation Competitive Hourly Pay Rate Additional shift differential for 2nd shift and 3rd shift positions Annual performance-based bonus Annual merit performance-based increase Excellent Benefits Benefits & Total Rewards | Thermo Fisher Scientific Medical, Dental, & Vision benefits-effective Day 1 Paid Time Off & Designated Paid Holidays 401K Tuition Reimbursement Employee Referral Bonus Career Advancement Opportunities Compensation and Benefits The hourly pay range estimated for this position based in California is $21.42-$35.70. This position may also be eligible to receive a variable annual bonus based on company, team, and/or individual performance results in accordance with company policy. We offer a comprehensive Total Rewards package that our U.S. colleagues and their families can count on, which includes: A choice of national medical and dental plans, and a national vision plan, including health incentive programs Employee assistance and family support programs, including commuter benefits and tuition reimbursement At least 120 hours paid time off (PTO), 10 paid holidays annually, paid parental leave (3 weeks for bonding and 8 weeks for caregiver leave), accident and life insurance, and short- and long-term disability in accordance with company policy Retirement and savings programs, such as our competitive 401(k) U.S. retirement savings plan Employees' Stock Purchase Plan (ESPP) offers eligible colleagues the opportunity to purchase company stock at a discount For more information on our benefits, please visit: *****************************************************

Shift: Monday-Friday: 7: 00AM-3: 30PM Duration: 12 Months Pay range: $25.45 Hourly - $25.45 Hourly Onsite Job How will you make an impact? Working in collaborative group environment, we manufacture high quality custom oligonucleotides in a high efficiency, fast paced setting. These oligos manufactured are used in a variety of applications including helping perform genetic research, diagnose disease and help with food supply. What will you do? You work with a team to Manufacture Custom Oligonucleotides for use in the biotech industry by following established protocols and SOPs. The team uses semi-automated and automated basic lab equipment. Regularly evaluate non-routine test results and either fail the product or allow it to continue through the production cycle. •Highly repetitive tasks for prolonged periods of time. •Understand scientific principles in order to problem solve, troubleshoot test results, evaluate alternative choices and exercise independent judgment in selecting the best solution. Provide multiple decision options and corresponding logic/data behind the decisions. Proactively identifies production problems. •Provides input and shares ideas and suggestions about improving lab techniques, protocols, processes, special handling of the product and equipment. •Balance multiple tasks. Demonstrate knowledge in the use of basic lab techniques and basic computer knowledge. Demonstrate ability to meet standards as defined by the manufacturing process. •Thoroughly and accurately complete documentation (completion of Batch Records, document data verifications, document problems, bring deviations to the attention of the Supervisor/Manager). •Continuously strive to improve output goals. Demonstrate good time management resulting in efficiency. Support cost improvement initiatives by reducing failures, improving capacity and using supplies wisely. Reduce work in process, queues and cycle times. •Advise appropriate people about problems/questions;be prepared to discuss problems/questions clearly. Work in a safe manner. Work with team members to overcome obstacles. Collaborate, support and consult with other team members as necessary. Give and receive feedback about individual and group performance •May be required to perform other related duties as required and/or assigned. Position occupies a significant role in mainstream oligonucleotide production. The role requires the ability to exercise judgment within generally defined practices and policies in selecting methods and techniques for obtaining solutions. How will you get here? •Degree in the bench sciences (Biology, Chemistry, etc) is preferred but a HS diploma can be considered. •Strong digital literacy including familiarity with relevant software (Excel and Word) are required. Experience •1 year of lab experience preferred (1 year maybe acquired through work or school). •Proven track record of working well with others in a collaborative team environment. Knowledge, Skills, Abilities •Operate in a fast-paced environment and while working as a team. •Efficient worker whom can multitask across multiple areas within the manufacturing environment. •Required to be able lift up to 20 lbs. •Ability to stand while performing duties. •Capable of working safely with chemicals and hazardous materials. •Capacity to work outside of regular work hours when business demands call for it. •The above position will require you to work a flexible shift pattern. Employee Benefits: At LanceSoft, full time regular employees who work a minimum of 30 hours a week or more are entitled to the following benefits: Four options of medical Insurance Dental and Vision Insurance 401k Contributions Critical Illness Insurance Voluntary Permanent Life Insurance Accident Insurance Other Employee Perks About LanceSoft LanceSoft is rated as one of the largest staffing firms in the US by SIA. Our mission is to establish global cross-culture human connections that further the careers of our employees and strengthen the businesses of our clients. We are driven to use the power of our global network to connect businesses with the right people, and people with the right businesses without bias. We provide Global Workforce Solutions with a human touch.

KO Business Solutions is a family-owned consulting firm proud to work with a manufacturing company in Elk Grove Village, IL who is seeking a Quality Control Inspector to join their production team.The Blasting Operator is responsible for the accurate and efficient production of product requiring abrasive blast in accordance with applicable specifications and process controls. Schedule: 7am -3:30pm Location: Elk Grove Village, IL Job-Type: Direct Hire, Full-time Pay-Rate: $24-$26/hr Position Overview: The Quality Control Inspector (QCI) is responsible for verifying that the work performed by MIL follows all applicable specifications, customer requirements, and expectations. This hands-on position will prioritize and complete critical inspections to consistently meet turnaround and quality requirements. Primary Job Responsibilities: Perform incoming, in-process, and final inspections against accept / reject criteria on customer parts while working with critical tolerances. Utilize mathematical skills and methods of tolerance analysis to determine potential removal/buildup of substrate regarding dimensional change. Understand, assess, and perform test methods using instruments such as micrometers, eddy current thickness testers, bore gages, gloss meters, etc. Perform contract / flow down review as needed, ensuring adherence to externally supplied documents including purchase orders, engineering drawings, specifications, and customer work instructions. Complete pertinent data records including job log entry, job routing package, inspection logs, job techniques and customer specific requirements. Operate precision measuring equipment such as micrometers, calipers, bore and thread gages, fixtures, microscopes etc. Review, complete and/or ensure adherence to the company's internal documentation including work orders, processing techniques, inspection reports, frozen plans, and the company's general procedures. Provide cross-functional support to QCI and QA personnel and contribute toward peripheral projects and tasks as needed. Recommend improvements to production to ensure quality control. Perform additional duties as assigned or required to support organizational goals and objectives. Participate in applicable ongoing training sessions, continuous process improvement programs, periodic testing, and performance evaluations. Knowledge, Skills, Abilities: Advanced GD&T skills. Ability to take tight tolerance measurements (+/- .00005 - .0002) while maintaining accuracy and throughput. Ability to perform calibration/verification on measurement tools. A detail-oriented, organized, self-starting individual with excellent written and verbal communication and interpersonal skills. Prioritize and complete tasks with consistency and accuracy, often under pressure and/or short deadlines. Develop and maintain a comprehensive technical understanding of the company's processing capabilities and quality system as well as general procedures and applicable industry standard specifications. Knowledge of plating, anodize, etching, or Nadcap principles is desirable. Minimum Job Requirements: High school degree or equivalent required. College degree preferred. Must have a minimum of 4 years of dimensional inspection experience in an aerospace / defense, avionics, medical, or similar industry. Experience evaluating and interpreting engineering drawings. PC proficient with a comprehensive understanding of Microsoft Office applications. Understanding of QA sampling plans including visual and dimensional examinations and other ancillary test methods strongly preferred. Bilingual in English / Spanish a plus. Individual must be authorized to work in the U.S. This position requires access to ITAR-controlled information and materials. The successful candidate must meet all ITAR eligibility requirements, including being a U.S. person as defined by ITAR. Benefits: Annual performance and compensation review, with eligibility for annual bonuses 401(k) plan with employer matching and profit sharing Premium health insurance as well as supplemental vision and dental insurance plans Company paid and supplemental life insurance and AD&D Company paid holidays and personal paid time-off (accrual & enrollment package) Equal Opportunity Employer KO Business Solutions is an equal opportunity employer that is committed to diversity and inclusion in the workplace. We prohibit discrimination and harassment of any kind based on race, color, sex, religion, sexual orientation, national origin, disability, genetic information, pregnancy, or any other protected characteristic as outlined by federal, state, or local laws. Job type: Direct Hire Rate of Pay: $24-$26/hr #INDH

Job DescriptionPosition: Chemical Technician Reports To: Senior Process Engineer Coreshell's metallurgical Silicon anode technology delivers high capacity, fast-charging, and superior safety. Our low-cost liquid-phase nano-coating addresses critical electrode-surface degradation issues and enables batteries with a Silicon-dominant anode that have higher energy density, superior intrinsic thermal safety, and significantly lower cost/kWh compared to current LIBs. Our Si anode material is 50% the cost of graphite and 100% domestically sourced. We strive to transform the global automotive market by enabling low-cost and long-range EVs as a first step towards net-zero sustainability in the near future. Core Responsibilities: We are looking for a Chemical Technician to execute on synthesizing materials with material characterization and data record on a regular basis. The ideal candidate has a strong background in chemistry with significant laboratory experience and can act on his/her own initiative to troubleshoot problems. Familiarity with material analysis is also desired. Responsibilities include: Assist scientists/engineers by synthesizing and characterizing new battery materials and new thin-film coating materials. Characterize inorganic/organic materials by analytical instruments. Follow SOPs and keep data records weekly. Keep accurate and detailed records of all laboratory activities, including experimental procedures, observations, and results Requirements: B.S. degree or equivalent in Chemistry, Chemical Engineering, Materials Science OR experience in a similarly relevant field with 2+ years of industrial experience. Previous experience with laboratory work (wet chemistry preferred). Completed Chemistry-related courses with laboratory component. Some previous experience on material characterization is preferred but not essential. Able to safely handle chemicals and safely work in a laboratory setting. Able to safely move equipment up to 20 kg. Interested in a career in science & technology and passionate about the clean energy space. Location & Benefits: San Leandro, CA. Full-time. Hourly rate is $26.00 - $35.00 per hour with additional stock incentives dependent on experience. Dental, vision, healthcare and 401(k) benefits are included. Applications will be screened as received. Powered by JazzHR R6idj72k5s

Axolabs is a business unit of LGC, and a leading provider of CRO / CDMO capability to the therapeutic oligonucleotide discovery and development industry. Centred out of LGC's site in Kulmbach, Germany, Axolabs works closely with its customers to assist the identification and development of lead candidates with a broad suite of bioinformatics, biology, chemistry, manufacturing and analytical services that support discovery, pre-clinical and clinical trials and scale-up manufacture. With a track record in Nucleic Acid Therapeutics that traces back more than 20 years, Axolabs provides deep knowledge and expertise in the services it provides, working collaboratively and responsively with its clients to assist them in achieving their objectives. Axolabs facility in Petaluma is focused on manufacturing scale-up and production to cGMP of multigram to kilograms of API for pre-clinical and clinical development. Our site in California has been involved in oligonucleotide synthesis for three decades and established the therapeutics activity in 2019. With around 70 staff and two manufacturing trains, Axolabs offers a flexible manufacturing service out of Petaluma that draws where necessary on our industry and chemical and analytical expertise in Kulmbach. Job Description This is an Swing Shift: Monday-Thursday (4 x 10 hours, 1pm - 11:30pm). The QC Associate Scientist brings scientific experience to LGC and is open to both learning more and sharing knowledge with others. You will be part of an ambitious and collaborative team that strives for flawless execution in all tasks. Setting up instrument sequences, while monitoring analysis and data Performing instrument troubleshooting, maintenance, and reporting of results for timely delivery to internal and external collaborators Coordinating routine and stability analysis, while driving continuous improvement via analytical methodologies Maintaining appropriate quality control processes and procedures to determine accuracy and precision of analysis Demonstrating a familiarity with GMP guidelines 21 CFR Part 210/211 and ICHQ7 Qualifications Minimum Qualifications: Science degree in Chemistry, Biology or similar with 2 years lab experience in manufacturing Must have strong organic chemistry and/or analytical chemistry knowledge, and proficiency in associated analytical techniques; HPLC, LC-MSMS or GC-MS Proficient in cGMP Solid understanding of analytical manufacturing support Preferred Qualifications: Experience in size exclusion, ion exchange, and reverse phase chromatography, KF, FT-IR and NMR techniques preferred Additional Information What we offer (US based-employees): Competitive compensation with strong bonus program Comprehensive medical, dental, and vision benefits for employees and dependents FSA/HSA Pre-tax savings plans for health care, childcare, and elder care Deductible Buffer Insurance and Critical Illness Insurance 401(k) retirement plan with matching employer contribution Company-paid short- and long- term disability, life insurance, and employee assistance program Pet Insurance for our furry friends Enhanced Parental leave of 8 additional weeks PTO that begins immediately Town Hall monthly meeting onsite/virtual, Cheer program where employees are recognized for outstanding work, Company wide social events and much more! The typical pay range for this role is: Minimum: $ 28.12 /Hourly Maximum: $ 43.19 /Hourly This range represents the low and high end of the anticipated salary range for the California -based position. The actual base salary will depend on several factors such as: experience, skills, and location. ABOUT LGC: LGC is a leading, global life science tools company, providing mission-critical components and solutions into high-growth application areas across the human healthcare and applied market segments. Its high-quality product portfolio is comprised of mission-critical tools for genomic analysis and for quality assurance applications, which are typically embedded and recurring within our customers' products and workflows and are valued for their performance, quality, and range. OUR VALUES PASSION CURIOSITY INTEGRITY BRILLIANCE RESPECT EQUAL OPPORTUNITIES LGC strongly believes that every job applicant and employee should be valued for their individual talents regardless of age, disability, race, color, ethnic or national origin, sex, sexual orientation, gender reassignment, marital or civil partnership, pregnancy or maternity, religion, or belief. Short listing, interviewing and selection will always be carried out without regard to gender, sexual orientation, marital status, color, race, nationality, ethnic or national origins, religion or belief, age, or trade union membership. For more information about LGC, please visit our website **************** #scienceforasaferworld