Quality control analyst jobs in North Las Vegas, NV

Formulation Technician I Duration: 12 Months Job Type: Temporary Assignment Work Type: Onsite Shift: Monday to Friday from 02:00 PM to 10:30 PM Pay Range: $20.00 to $25.00/hr. Overview TekWissen is a global workforce management provider headquartered in Ann Arbor, Michigan that offers strategic talent solutions to our clients world-wide. The job opportunity below is for one of our clients specializing in biotechnology product development services. Our client is dedicated to supplying laboratory equipment, chemicals, supplies, and services essential in healthcare, scientific research, safety, and education. As the global leader in serving the field of science, our client boasts an annual revenue of around $40 billion with a mission to empower customers to make the world healthier, cleaner, and safer. Our client's global team is committed to delivering an unparalleled blend of cutting-edge technologies, convenient procurement options, and pharmaceutical services under their industry-leading brands. Summary: Work in a team-based manufacturing lab environment within the Chromatography and Mass Spectrometry Division (CMD) in Sunnyvale, CA. Responsible for synthesizing and testing ion exchange media used in chromatography consumables. Responsibilities: Test resin products on specialized instruments to meet customer demand. Record and report test results accurately and maintain proper documentation. Complete production work orders according to established procedures. Follow corporate quality policies to ensure high-quality standards. Follow safety requirements and actively participate in safety improvement activities. Maintain a clean and organized laboratory environment. Required Skills: High school diploma or equivalent. Previous work experience in manufacturing, operations, production, or a lab setting or related field. Knowledge of Good Laboratory and Manufacturing Practices and standards. Good mathematical, problem-solving, and organizational abilities. Excellent verbal and written communication skills. Ability to read and understand written procedures (SOPs) and follow verbal instructions. Familiarity with commonly used hand tools (wrenches, torque drivers, tweezers, etc.). Proficiency with spreadsheet and database software. Ability to lift and/or move up to 40 pounds. Ability to sit, stand, walk, and use hands/fingers to handle and feel small components. Visual ability to detect small components and particles. TekWissen Group is an equal opportunity employer supporting workforce diversity

* Perform routine inspections on samples and equipment to ensure accuracy and compliance * Document findings, track results, and report any issues or deviations * Follow established lab protocols to maintain safety and quality standards * Support the team by helping troubleshoot errors and improving processes Determining compensation for this role (and others) at Vaco/Highspring depends upon a wide array of factors including but not limited to the individual's skill sets, experience and training, licensure and certifications, office location and other geographic considerations, as well as other business and organizational needs. With that said, as required by local law in geographies that require salary range disclosure, Vaco/Highspring notes the salary range for the role is noted in this job posting. The individual may also be eligible for discretionary bonuses, and can participate in medical, dental, and vision benefits as well as the company's 401(k) retirement plan.

CHROME HEARTS , the Fine Jewelry, Accessories, Shoes, Fragrance & Home Goods company renowned for its sophisticated life-inspired designs, was conceived in 1988 by Richard Stark in Los Angeles. Honoring a commitment to quality materials and timeless design, CHROME HEARTS now has thirty+ stores across North America, Europe, and Asia, and can be found in the most exclusive boutiques around the world. SUMMARY/OBJECTIVE We are looking for an experienced and detail-oriented Quality Control (QC) Specialist. The ideal candidate will be responsible for ensuring that all products meet the required quality standards throughout every stage of the production process - from raw material inspection to final product verification. ESSENTIAL FUNCTIONS Perform in-line and final quality checks to ensure compliance with technical and quality specifications. Collaborate with production, procurement, and development teams to identify and resolve quality-related issues. Prepare and maintain up-to-date quality control reports and documentation. Identify recurring issues and propose improvements to production processes. Ensure compliance with company standards, customer requirements, and industry regulations. Participate in quality audits and support supplier and subcontractor assessments. Train internal staff and production partners, when needed, on quality standards and control procedures. QUALIFICATIONS 1 year of experience in quality control within luxury manufacturing environments. Solid knowledge of inspection techniques, production processes, and common quality issues. Proven experience working with suppliers and manufacturing sites, both domestically and internationally. Strong attention to detail, analytical skills, and problem-solving abilities. Ability to work independently and manage multiple tasks in a dynamic environment. Proficiency in Microsoft Office (Excel, Word). Experience with AQL QC reporting is a plus. Willingness to travel regularly for inspections and visits to production sites. Good command of written and spoken English. BENEFITS 401(k) matching Dental insurance Health insurance Life insurance Paid time off Vision insurance The pay range for this role is: 22.00 - 24.00 USD per hour (Hollywood, CA )

With a legacy spanning over 35 years, Harris Spice has been a trusted partner and leading supplier of high-quality spices, herbs, and innovative seasoning blends. With international facilities and a global supply chain, we proudly serve multiple channels of trade-including industrial bulk, food service, and retail. Our commitment to excellence, quality and consistency has earned us the trust of some of the nation's largest and most recognized brands. As Harris Spice continues to grow, we are dedicated to cultivating a dynamic, inclusive workplace where innovation thrives. We're looking for diverse, talented individuals who are ready to grow with us and help strengthen a brand known for trust, quality, and bold flavor solutions. Position Overview/Job Summary: We are looking for a 1st shift (4:30am-1:00pm) Quality Control Technician to join our team. The Quality Control Technician is responsible to ensure food safety and quality of plant through enforcement of HACCP, and Good Manufacturing Practices (GMPs) are followed by all personnel and to confirm each product meets specifications and quality parameters. Essential Job Functions: Performing pre-operational inspections at beginning of shift or production line changeovers to achieve on-time start-up and first-time quality. Collect raw material samples upon receipt and report any discrepancies to Quality Manager. Verify correct raw materials and packaging are being picked, staged, and used in production. Determine the acceptability of products using visual inspections, sampling, and testing protocols (when necessary). Perform detail-oriented tasks to support production such as checking legible lot codes, “best by” dates, container seals, handling production line rejects, etc. Enforce good manufacturing practice Provide support to the production department to minimize downtime and run efficiently. Maintain orderly paperwork and verify accurate documentation among production, quality, sanitation, maintenance, warehouse, and R&D departments. Organize production and quality records by following established protocol. Perform, log, and verify metal detector checks and provide training to production coworkers. Escalate issues of non-conforming products in a timely manner to management and segregate or place on hold. Interact and support cross-functional department personnel and adapt to change in a fast-paced environment. Ability to work with minimum supervision. Follow and enforce personal safety procedures and escalate to management. Other duties as assigned. This position has no direct reports but may assist in training coworkers and/or covering absences. This describes just some of the main duties, activities and responsibilities for the role which may change at any time with or without prior notice. Skills/Qualifications: 1-2 years of experience in a quality or lab role, preferably within a food manufacturing environment. Knowledge of sanitary food lab techniques and equipment. Able to read Standard Operating Procedures and follow instructions. Able to interpret product specifications. Good communication skills Understand and apply company and customer quality standards. Comfortable working with Microsoft Office and other production or lab information systems as needed. English fluency required, bilingual Spanish a plus. Physical Requirements: Ability to stand in a lab environment, ability to lift 55lbs, and handle food samples in a sanitary manner Sit, use hands & arms, twist, bend, push or pull Walking, standing, stooping, bending, kneeling, pulling, pushing, twisting, climb etc. The statements herein are intended to describe the general nature and levels of the work performed by employees, but are not a complete list of responsibilities, duties, and skills required of personnel so classified. Furthermore, the job description does not constitute a written or implied contract for employment. Harris Spice reserves the right to revise or change job duties and responsibilities as the need arises. Equal Employment Opportunity Statement Harris Spice is a certified Minority-owned business. Our business is an equal opportunity employer committed to a diverse and inclusive workforce. Applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy), age, sexual orientation, national origin, marital status, parental status, ancestry, disability, gender identity, veteran status, genetic information, other distinguishing characteristics of diversity and inclusion, or any other protected status.

The QC-C Inspector monitors shop production for fit-up and welding of structural steel members and parts under the direct supervision of QC-B and -A inspectors. They are responsible for the implementation of the SME Industries Quality Control program and all Company standards. Inspectors need a good understanding of the codes and standards of the industry and SME's manufacturing system. The Inspector must be familiar with the inspection and welding processes as used in the industrial and commercial industry. ABOUT US: Southwest Steel is a steel fabrication and erection company that specializes in miscellaneous metal, steel stairs, railings, structural steel, and creatively unique custom steel pieces to complete projects from standard building needs to anything imaginable. Visit ********************** to learn more. Southwest Steel is a division of SME Industries, Inc. Why Join Us? Health and Wellness Benefits including Medical, Dental, Vision, Short Term Disability and Life Insurance. Financial Benefits including competitive compensation and 401(k) plan. Additional Benefits including Paid Holidays and Paid Time Off, Employee Assistance Program, and more. ESSENTIAL DUTIES AND RESPONSIBILITIES: Perform assigned duties within the requirements of the Project specifications, codes and standards as defined in contract documents and Company Quality Management system. Learn to review drawings for accuracy and provide interpretation for production personnel where needed through the fabrication process. Assist in monitoring welding and inspection equipment for compliance, ensure personnel are qualified and certified to operate the equipment. Assist in the performance of 100% visual welding inspection for weld quality, size and location. Provide dimensional verifications of fabricated members, as time allows, for compliance with industry standards. Learn the appropriate documentation for these inspections, testing and qualifications. Assist in completing Non-conformance reports and follow up on corrective actions. Assist in the performance of non-destructive testing of welds and materials. Study and keep current with new editions of the codes and standards. Perform duties in a timely manner to ensure contract scheduling issues. Maintaining inspection and test equipment in proper order, ensure equipment is properly calibrated for the work performed. Keep work area orderly and clean. Comply with the code of ethics for Inspectors as provided by the American Welding Society. Perform additional assignments as directed by the QA Supervisor. QUALIFICATIONS: Must be able to perform each essential duty daily. High School diploma, GED or equivalent, and 2 years of previous welding or Quality Control experience or similar trade school. Must be dependable, reliable, and mature enough to handle equipment in a safe and sensible manner. Ability to do simple math and/or algebraic formulas as deemed necessary by work type. The ability to understand the working mechanism of tools and machinery under their responsibility. Ability to communicate equipment problems, production quality numbers, and quality issues with proper individuals. Attend to detail; ability to communicate verbally and in writing, if necessary, with subordinates, co-workers, maintenance, supervisors and inspectors. Inspector in training or one holding a single in-hour certification. PHYSICAL DEMANDS: Must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions on a case-by-case basis in conjunction with the official Company doctor and clinic. Ability to lift and carry up to 50 pounds regularly and up to 65 pounds occasionally. Must be able to stand, kneel, bend, twist, and reach for extended periods and work from scaffolding and/or ladders as required. Physically fit to work in an industrial environment and tolerate exposure to varying physical conditions. Must be able to work extended hours when necessary. Manual dexterity and hand-eye coordination to operate tools, equipment, and safety devices. Tolerance to loud noises, vibrations, dust, heat, and fumes within a fabrication shop environment. Ability to wear required PPE (Personal Protective Equipment) includes safety glasses, gloves, steel-toed boots, high visibility clothing, and hearing protection. WORK ENVIRONMENT: Industrial warehouse and manufacturing environment with heavy machinery, and overhead cranes. Strict adherence to safety procedures and use of PPE is always mandatory. Frequent interaction with production staff, supervisors, safety personnel, and quality control teams. Exposure to hot and cold temperatures, depending on seasonal conditions. Position Responsibilities:This job posting reflects the current assignment of essential functions and is not meant to be all-inclusive. Duties and responsibilities may be assigned or reassigned to this position at any time. Equal Employment Opportunity: SME Industries, Inc. and its divisions (SME Steel Contractors, Southwest Steel, CoreBrace, DuraFuse, and SME Logistics) is an Equal Opportunity (EEO) Employer. All qualified applicants will receive consideration without regard to race, color, national origin, sex, sexual orientation, gender identity, religion, age, status as a protected veteran, status as an individual with disability, or any other protected group status or non-job-related characteristic as directed by law. Employment Authorization: Applicants must be legally authorized to work in the United States without the need for employer-sponsored work authorization now or in the future. Proof of eligibility will be required upon hire.

Stock Room Clerk - Santa Ana, CA 5:00 AM - 1:30 PM | Monday-Friday | Temp-to-Hire $20 per hour Seeking a reliable Stock Room Clerk to handle inventory, organize materials, and support production needs. Must be computer literate and dependable. Must be able to work overtime when needed. Desired Skills and Experience Stock Room Clerk - 1st Shift Santa Ana, CA | 5:00 AM - 1:30 PM | Monday-Friday | Temp-to-Hire $20 per hour Seeking a reliable Stock Room Clerk to handle inventory, organize materials, and support production needs. Must be computer literate and dependable. All qualified applicants will receive consideration for employment without regard to race, color, national origin, age, ancestry, religion, sex, sexual orientation, gender identity, gender expression, marital status, disability, medical condition, genetic information, pregnancy, or military or veteran status. We consider all qualified applicants, including those with criminal histories, in a manner consistent with state and local laws, including the California Fair Chance Act, City of Los Angeles' Fair Chance Initiative for Hiring Ordinance, and Los Angeles County Fair Chance Ordinance. For unincorporated Los Angeles county, to the extent our customers require a background check for certain positions, the Company faces a significant risk to its business operations and business reputation unless a review of criminal history is conducted for those specific job positions.

We are seeking a QC Chemist to join our growing team. The QC Chemist performs routine and non-routine chemical analyses of raw materials, in-process samples, and finished products to ensure product quality and regulatory compliance. This role supports production troubleshooting, laboratory operations, and continuous improvement activities within the Quality Control function. Primary Responsibilities Perform qualitative and quantitative chemical analysis using techniques such as GC-MS, LC, FTIR, UV-Vis, Rheology, Particle Size Analysis, Spectrophotometry, titration, wet chemistry, and basic microbiological testing. Conduct method validations, verifications, and transfers as assigned. Execute testing of raw materials, intermediates, finished goods, and stability samples according to established methods, SOPs, and regulatory requirements. Review, interpret, and document analytical data clearly and accurately in laboratory notebooks and electronic data systems. Support investigations of OOS (Out-of-Specification) and OOT (Out-of-Trend) results, including root cause analysis and CAPA activities. Make material disposition decisions (Approve / Reject / Rework) based on analytical results. Calibrate and maintain laboratory equipment in alignment with internal procedures. Ensure testing activities adhere to cGMP, GLP, and applicable quality standards. Train and mentor junior laboratory staff as required. Assist in preparing for internal and external audits, providing data and documentation. Support preparation and revision of SOPs, test methods, and laboratory records. Maintain a safe, organized, and compliant laboratory environment. Perform additional related duties as needed. Minimum Requirements 4-5+ years of experience in a Quality Control or Analytical Laboratory environment (required). Bachelor's degree in Chemistry, Biochemistry, or related scientific field (required); Master's degree preferred. Experience in cGMP-regulated manufacturing environments (cosmetics, pharmaceuticals, chemicals, food science, or nutraceuticals). Solid understanding of cGMP, GLP, and regulatory documentation standards. Experience with LIMS or other electronic laboratory data systems (preferred). Knowledge, Skills, & Abilities Strong analytical, problem-solving, and troubleshooting skills. Excellent documentation accuracy and attention to detail. Clear written and verbal communication skills. Ability to prioritize and manage multiple tasks in a fast-paced environment. Collaborative work style with strong interpersonal skills. Proficiency in Microsoft Office (Excel, Word, Outlook, Teams) and general data analysis.

Job Title: QC/Internal Audit Analyst - Mortgage Servicing & Originations Job Type: Full Time Company: Village Capital & Investment LLC Introduction: Village Capital is a well-established mortgage company committed to delivering a quick, efficient, and quality mortgage loan process to our customers and business partners. We are a nationwide mortgage lender specializing in FHA, VA, USDA Loans. Our Headquarters are located in Henderson NV. We are a lender/servicer, who works with loan originators, brokers, and correspondents to offer our customers great rates and good terms. Key Responsibilities: Conduct independent quality control audits on mortgage originations and servicing to ensure compliance with regulatory, investor, and company guidelines. Identify and report operational, regulatory, or compliance risks, recommending corrective actions and supporting remediation efforts. Review loan files for adherence to federal, state, and investor requirements (e.g., RESPA, TILA, ECOA, CFPB, Fannie Mae, FHA, VA). Prepare audit reports, track findings, and provide data analysis and trending insights for management. Collaborate with internal teams and support external audits while staying informed on industry regulations and guideline updates. Basic Qualifications: Proven experience with problem-solving skills and attention to detail. Strong communication and interpersonal skills. Ability to work independently and as part of a team with minimal supervision and exercise sound judgement. Proficiency in Windows and Encompass (Encompass preferred). Strong problem-solving skills and attention to detail. Specific Qualifications: 1-3 years of mortgage industry experience with expertise in both loan originations and servicing. In-depth knowledge of federal and state mortgage regulations (e.g., RESPA, TILA, TRID, ECOA, HMDA, FDCPA, CFPB). Experience in quality control, compliance, internal audit, or risk management, with familiarity with agency, government, and private investor guidelines. Strong analytical, attention-to-detail, and communication skills, including effective report writing. Proficiency in mortgage systems like Encompass or MSP, with the ability to handle multiple audits and deadlines efficiently. Benefits: 401(k) matching Dental insurance Health insurance Health savings account Life insurance Paid time off Vision insurance In summary: If you are looking for an opportunity to contribute to a growing organization that values your skills and expertise, we want to hear from you. At Village Capital and Investment LLC, we believe in fostering a supportive and inclusive work environment that encourages professional growth. Apply today to take the next step in your career with us!

Artech is the 10th Largest IT Staffing Company in the US, according to Staffing Industry Analysts' 2012 annual report. Artech provides technical expertise to fill gaps in clients' immediate skill-sets availability, deliver emerging technology skill-sets, refresh existing skill base, allow for flexibility in project planning and execution phases, and provide budgeting/financial flexibility by offering contingent labor as a variable cost. Job Description • Vaccine Immunotherapeutics (VITx) seeks to Client Client vaccines (prophylactic and therapeutic) for the prevention and treatment of significant human using a variety of vaccine technology platforms combined with immunomodulatory agents. • A virus purification scientist is required to join Vaccine Immunotherapeutics in La Jolla, California, to develop and support vaccine platform production processes at the research scale. • The candidate will have solid training and knowledge in virus/protein purification. • The candidate will be able to independently and proactively apply this knowledge in the design and execution of experimental work, to enable progression of vaccine discovery projects. • Experience in most or all of the following areas are desirable- protein/virus purification using chromatographic techniques, experience with Unicorn based FPLC systems, tangential flow ultrafiltration, dead-end filtration and ultracentrifugation based purification. • Additional desirable skills would include virus/protein characterization techniques and experience in handling Cat.2 infectious viruses. • The candidate will be required to work semi-independently and, as a member of a team, be accountable for the critical appraisal of their results and present them for review, at specific project milestones. • The role is laboratory based, and a major emphasis is placed upon laboratory training to increase the scope of practical abilities, as well as the theory behind such practical work. Additional Skills: protein/virus purification using chromatographic techniques, experience with Unicorn based FPLC systems, tangential flow ultrafiltration, dead-end filtration and ultracentrifugation based purification. Additional desirable skills would include virus/protein characterization techniques and experience in handling Cat.2 infectious viruses. Expected qulaifications/experience BSs or MSc in biological sciences or biochemical/chemical engineering At least 1-5 years working in a laboratory in an academic or industrial setting Additional Information Best Regards, Anuj Mehta ************

Scientist, Protein Production and Characterization AlivaMab Biologics is a rapidly growing leader in the discovery of human antibody therapeutics, trusted by top-tier pharmaceutical and biotechnology companies to deliver panels of drug-quality human antibodies. We deliver on our partners' design goals, from simple to extraordinarily challenging, through collaborative access to our scientists' creativity and experience combined with proven technologies, including the AlivaMab Mouse suite of transgenic mice. Our organization is dedicated to creating a healthier world through partnerships that bring better medicines to patients faster, and we recognize our success starts with hiring people who share our passion for science. We are seeking a highly motivated and skilled Scientist to join our Protein Sciences team and contribute to both day-to-day operations and the advancement of Protein Science workflows. This position will focus on the design, optimization, and execution of transient transfection processes at various scales for antibody and protein production in mammalian expression systems. The successful candidate will leverage expertise in biophysical characterization and biochemical modification to evaluate key protein attributes. This position will report to the Associate Director of Protein Sciences and work closely with scientists in the Antibody Discovery, Antibody Engineering, Protein Sciences, and Project Management teams. The ideal candidate will drive innovation through process refinement, high-throughput automation, and growing proficiency of chemical conjugation techniques. This role offers the opportunity to work in a fast-paced, collaborative research environment, where creative solutions and a strong scientific approach are key to success. Responsibilities Responsibilities: Independently design, plan, and execute transient transfection workflows for antibody and protein production across various mammalian expression systems Develop, design, and optimize protein purification methods to enhance throughput, quality, and efficiency, as required Lead developability assessment studies by designing and conducting analytical experiments to evaluate protein stability, purity, and key biophysical characteristics Support production of complex construct design strategies (e.g VLPs, nanodiscs etc.), to enable immunization antibody discovery campaigns against challenging targets Drive implementation of automated high throughput processes to support protein production workflows using Bravo, and other robotic systems Maintain meticulous experimental records using electronic notebook (Benchling), and communicate results clearly through written reports and presentations to support project progression and scientific decision-making Contribute innovative ideas and collaborate effectively across teams to foster research excellence and ensure project success in a fast-paced environment Qualifications Qualifications: Ph.D. in Biochemistry, Chemistry, Molecular Biology, Protein Engineering, or a related field with a minimum of 2 years of industry experience or MS with minimum of 6 years of direct industry experience is required Proven hands-on experience with multiple mammalian expression platforms is required Proficiency with AKTA instrumentation, and a broad range of purification techniques, including affinity chromatography, ion exchange, HIC, and SEC, as well as standard protein QC methodologies is required Experience with therapeutic antibody developability assessment is highly desirable Strong analytical, troubleshooting, and communication skills with exceptional attention to detail Motivated self-starter with excellent organization, teamwork, and a passion for scientific innovation About AlivaMab Biologics AlivaMab Biologics sets its partners' antibody discovery programs on the fastest and most de-risked path through discovery and development. Trusted by top-tier pharmaceutical and biotechnology companies, AMB delivers drug-quality, fully human antibodies on exceptional timelines. AMB achieves its partners' design goals, from simple to extraordinarily challenging, through the generation and function-first screening of large, molecularly diverse panels of antibodies. AMB focuses on rapid and efficient delivery of antibodies, characterized for function, kinetics and developability, and engineering for alternative formats, including multi-specifics and CARs. The AMB team's experience and passion for antibody drug discovery and development combined with the use of trusted, proven technologies, including Ablexis' AlivaMab Mouse platforms, ensure the highest probability of success. The salary range for this position considers various factors, including skills, experience, training, certifications, and organizational needs. Note that this range does not reflect any geographic adjustments based on the location where the role will be based. At AlivaMab Biologics, it is uncommon for a new hire to start at or near the top of the salary range, as compensation is tailored to each individual's skills and breadth and depth of experience. The current estimated range is $98,500 - $140,000, plus a bonus target, benefits, and equity. AlivaMab Biologics provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to religion, race, creed, color, sex, sexual orientation, gender identification, alienage or citizenship status, national origin, age, marital status, pregnancy, disability, veteran or military status, predisposing genetic characteristics or any other characteristic protected by applicable federal, state or local law. #LI-DNI

Working in a team of media process technicians, media process technician I will manufacture dehydrated and liquid cell culture media. Formulation technician will be able to follow batch record instructions and will be expected to weigh microgram to kilograms quantities of individual raw materials, calibrate equipment, follow safety policies and procedures, operate milling equipment, perform sterile filtration and any other tasks required to complete cell culture media manufacturing. Standard product testing, such as osmolality, pH and turbidity, will also be performed in this job. This position works closely with R&D, procurement, quality, process technology, marketing as well as external and internal customers and vendors RESPONSIBILITIES: Responsible for the staging and compounding of raw materials within weight tolerances (e.G. Micrograms to kilograms), milling, blending, aseptic liquid filling, process control monitoring and documentation of such procedures for manufacturing dehydrated culture media and liquid media in accordance with production schedules following the appropriate GMP and department procedures Completes all required documentation neatly, accurately, and in accordance with GMP. Performs cleaning, inspection, calibration and assists in the maintenance of equipment. Maintains related logs and records. Performs equipment troubleshooting. Handles raw materials per GMP and Safety requirements. Uses equipment such as pipettors, balances, osmometer, turbidimeter and pH meters. Ensure that tasks are performed in a safe and responsible manner to create an injury free and incident free workplace Required to follow through on assigned responsibilities and able to function under supervision. Responsible for promoting positive team environment through good communications and team engagement. May be required to work overtime. Performs other duties as assigned in support of business goals QUALIFICATION REQUIREMENTS: Minimum of High School Diploma or equivalent. Minimum of 6 months experience in a high-paced laboratory environment or manufacturing facility. Equivalent combination of education, training, and relevant work experience maybe considered. Must be able to read, write, and follow testing and inspection procedures. Must be able to maintain neat, accurate and complete records and logs. Mechanical aptitude and ability to disassemble and reassemble various equipment. Good communication skills and ability to work both individually and as part of a team. Flexibility with departmental work schedules including overtime. Must be able to focus with continuous attention to detail. Basic experience in weighing multiple components is required. Basic proficiency with PCs (Personal Computers) and use of Windows applications such as MS Excel, MS Word and MS PPT is required. Statistical analysis using mathematical spreadsheets such as Excel or Minitab is highly desired. Must be able to lift or move approximately 40lbs 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.

Job Description Ignite Your Career at Unimacts: Powering Renewable Energy's Future! Ready to be a part of something monumental? Unimacts is on the cutting edge of contract manufacturing and supply chain management in the solar and wind sectors. With operations spanning the globe-from the U.S. and Mexico to Spain, India, and China-we're making waves in renewable energy markets. Thanks to the groundbreaking Inflation Reduction Act, we're poised for unparalleled growth in the solar industry. And guess what? Our parent company is backed by some of the most esteemed venture capital firms that have invested in globally recognized, VC-backed companies. It's an electrifying time to join us! Join the Unimacts team as a Quality Control Technician at our vibrant hub in Sloan, NV. Step into a role where “industrial business athletes” thrive, showing versatility and proactive involvement in shaping the development of our US plant and fortifying local supply chain capabilities. Be ready to both lead and immerse hands-on where needed, ensuring we meet all company and customer requisites. We are seeking a Quality Control Technician for 1st Shift (7AM-4PM). Responsibilities Quality Assurance: Leveraging analytical equipment and hand gauges to inspect, test, and measure products, components, and materials meticulously. Equipment Maintenance: Ensuring the optimal functioning of equipment used to validate adherence to customer specifications. Documentation and Reporting: Creating precise dimensional records and reviewing quality documentation for complete accuracy. Report findings promptly to the supervisor and initiate appropriate actions. Process Audits: Conducting process audits to ascertain process control and fostering continuous improvement initiatives in collaboration with the Maintenance/Production teams. Safety and Training: Embracing a culture of safety by attending meetings and training sessions and strictly following all safety guidelines. Material Inspection: Executing incoming inspection control for raw materials to secure the quality of the process. Requirements A high school diploma (associate degree is a substantial plus). At least 1 year as a Quality Technician in a manufacturing or industrial setting. A background in the Steel Rolling Industry is preferred. Familiarity with a range of gauges, Lean manufacturing, and continuous improvement approaches, with Six Sigma certification as a desirable attribute. Experience with ERP systems and manufacturing software is favored. Technical Proficiency: The ability to read and decipher drawings, specifications, and work instructions with a firm grasp on GD&T interpretation and measurement techniques. Communication Excellence: Masterful communication skills to report quality non-conformities, coupled with bilingual proficiency in English/Spanish, would be a significant asset. Documentation Skills: Expertise in documenting audit findings and quality checks clearly and concisely. Organizational Prowess: An innate talent for organization, adept at multitasking in a fast-paced environment, showcasing urgency and attention to detail.

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 98,000 employees operate a network of 2,650 offices and laboratories, working together to enable a better, safer and more interconnected world. Our Las Vegas, NV laboratory is looking for an entry-level Laboratory Analyst to join their team! The Laboratory Analyst prepares and analyzes samples with accuracy and precision in accordance to SGS' analytical SOPs. The Laboratory Analyst works independently and as part of a team to meet daily production targets and ensure hold times and turnaround times are met. The Laboratory Analyst understands and applies basic analytical chemistry principles. The Laboratory 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 May assist with validation and MDL studies. Assists with investigation, and preparation of responses to client inquiries and CARs. Inputs and maintains technical information as needed to support the laboratory functions/operations. Maintains Laboratory Notebook where applicable. Adheres to internal standards, policies and procedures. Performs other duties as assigned. Qualifications Associate Degree in a Chemistry or similar scientific discipline and 0-2 years of experience in Analytical Chemistry Laboratories OR 3 years of relevant experience (i.e. Sample Prep) (Required) Bachelor's Degree in a Chemistry or similar scientific discipline and 1-2 years of years' relevant experience in Analytical Chemistry Laboratories (Preferred) Basic mathematical and reasoning skills (Required) Experience with Microsoft Office (Excel, Outlook, Word) (Required) Experience with LIMS (Preferred) Ability to lift/carry/push and/or pull upwards of 25 lbs on a frequent basis (Required) 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.

THE ROLE: QA Lab Supervisor * Travel Requirement: N/A * FLSA Status: Hourly Non-Exempt * Employment Category: Full Time Regular * Pay Range: $20.25 - $22.75 Generous Brands is dedicated to inspiring people to thrive through the power of vibrant nutrition through its leading brands, Bolthouse Farms, Health-Ade, and Evolution Fresh. Generous Brands partners with SAMBAZON to manufacture, distribute and sell SAMBAZON branded beverages. Bolthouse Farms is a pre-eminent provider of chilled juice, smoothies, shakes, and protein drinks. Health-Ade is the fastest growing kombucha brand, dedicated to creating bubbly beverages that boost gut health. Evolution Fresh is a premier cold-pressed juice brand with national availability. And, SAMBAZON beverages bottle the superfruit power of acaí in juice and natural energy cans. The company operates its North American business from facilities in Southern California, and the Greater Chicago Area. To learn more, please visit *********************** WHAT YOU'LL BE RESPONSIBLE FOR IN THIS ROLE The Microbiology Lab Tech will execute the daily laboratory operation and ensure that the Laboratory Quality Management System is implemented and maintained in accordance with ISO 17025 standards. This position will handle data/report and resources (equipment, supplies) to ensure that required testing is completed. WHAT WE'RE LOOKING FOR * Maintain records and manages all aspects of testing activities * Prepare media and agar plates for testing and recording on media logs * Perform pour & petrifilm plating, count plates and record results * Report out of specification conditions and summarize test results * Perform sample preparation and testing of raw materials, finished products and others * Complete data/information recording, follow the status of testing, generating reports and communicating findings of those test results supporting the manufacture of quality products * Run membrane filtration (water testing method) and PCR method and record results * Maintain the safety, cleanliness and hygienic laboratory work environment including periodic/planned maintenance, cleaning and monitoring of equipment and the work areas * Follow lab safety protocols to maintain lab hygiene and eliminate cross contamination * Participate in proficiency program and test control samples * Assist or perform other duties/projects as assigned ADDITIONAL REQUIRED QUALIFICATIONS: * Ability to operate microbiology instruments and equipment including equipment preventive maintenance, calibration, checks and verification * Ability to perform microbiological swabbing and air monitoring (e.g. environment program for the micro lab) * Ability to work alone and as part of a team to ensure the department goals, accuracy, and timeliness and cost effectiveness are met * Show competency through successful completion of proficiency testing MINIMUM QUALIFICATIONS: * Associate degree is required or bachelor's degree in one of the following areas: Food Science, Microbiology, Chemistry, Biochemistry or related areas. Equivalent experience in a related field can be substituted for education * Math skills combined with the ability to perform and understand scientific based tests and results * Ability to communicate effectively in oral and written forms * Knowledge of computer applications such as Microsoft Office Excel, Word, etc. * Communicate and interact well with others in the laboratory and manufacturing environment * Ability to work with minimal supervision and apply Good Laboratory Practices * Valid Driver's License PREFERRED QUALIFICATIONS: * Some experience in Microbiology/Chemistry lab in the food-processing environment PHYSICAL DEMANDS & ENVIRONMENTAL HAZARDS: * The work environment for this position will be typical of the manufacturing facility. There are portions of the job that will require working in cold (< 40°F) environments, in warm environments (>90°F), and loud environments. * Must be able to work in a wet, cold, or hot environment * Must be able to lift up to 50lbs HOURS & WORKDAYS: * 2nd shift, workdays will vary, 2:00pm - 10:30pm & 4:00pm - 12:30am when business requires overtime and weekends will be mandatory. WHAT WE OFFER plus more! Our rich benefits packages are designed to support the health and well-being of both our eligible team members and families. * Medical, Dental & Vision * Group Life and AD&D * Voluntary Life and AD&D * Group Short & Long-Term Disability * 401(k) * Paid Time Off * Flexible Spending Accounts * Employee Assistance Program * Gym Membership Discounts EQUAL EMPLOYMENT OPPORTUNITY We are an equal opportunity employer committed to fostering a culturally diverse organization. We strive for inclusiveness and a workplace where mutual respect is paramount. We encourage applications from a diverse pool of candidates, and all qualified applicants will receive consideration for employment without regard to race, color, ethnicity, religion, sex, age, national origin, disability, sexual orientation, gender identity and expression, or veteran status. We will provide reasonable accommodation for qualified individuals with disabilities, as needed, to assist them in performing essential job functions. REASONABLE ACCOMMODATIONS Reasonable accommodations will be made to enable individuals with disabilities to perform the essential functions. If you are interested in applying for employment with Generous Brands and need special assistance to apply for a posted position, or if you believe you do not meet any of the required qualifications of a posted position due to a protected disability and would like to explore the possibility of an accommodation, please contact our Talent Acquisition team at *******************************. RECRUITMENT AGENCIES: Confidential does not accept unsolicited agency resumes. Generous Brands is not responsible for any fees related to unsolicited resumes. 2nd shift, workdays will vary, 2:00pm - 10:30pm & 4:00pm - 12:30am when business requires overtime and weekends will be mandatory.

Job Description THE ROLE: QA Lab Supervisor Travel Requirement: N/A FLSA Status: Hourly Non-Exempt Employment Category: Full Time Regular Pay Range: $20.25 - $22.75 Generous Brands is dedicated to inspiring people to thrive through the power of vibrant nutrition through its leading brands, Bolthouse Farms, Health-Ade, and Evolution Fresh. Generous Brands partners with SAMBAZON to manufacture, distribute and sell SAMBAZON branded beverages. Bolthouse Farms is a pre-eminent provider of chilled juice, smoothies, shakes, and protein drinks. Health-Ade is the fastest growing kombucha brand, dedicated to creating bubbly beverages that boost gut health. Evolution Fresh is a premier cold-pressed juice brand with national availability. And, SAMBAZON beverages bottle the superfruit power of acaí in juice and natural energy cans. The company operates its North American business from facilities in Southern California, and the Greater Chicago Area. To learn more, please visit *********************** WHAT YOU'LL BE RESPONSIBLE FOR IN THIS ROLE The Microbiology Lab Tech will execute the daily laboratory operation and ensure that the Laboratory Quality Management System is implemented and maintained in accordance with ISO 17025 standards. This position will handle data/report and resources (equipment, supplies) to ensure that required testing is completed. WHAT WE'RE LOOKING FOR Maintain records and manages all aspects of testing activities Prepare media and agar plates for testing and recording on media logs Perform pour & petrifilm plating, count plates and record results Report out of specification conditions and summarize test results Perform sample preparation and testing of raw materials, finished products and others Complete data/information recording, follow the status of testing, generating reports and communicating findings of those test results supporting the manufacture of quality products Run membrane filtration (water testing method) and PCR method and record results Maintain the safety, cleanliness and hygienic laboratory work environment including periodic/planned maintenance, cleaning and monitoring of equipment and the work areas Follow lab safety protocols to maintain lab hygiene and eliminate cross contamination Participate in proficiency program and test control samples Assist or perform other duties/projects as assigned ADDITIONAL REQUIRED QUALIFICATIONS: Ability to operate microbiology instruments and equipment including equipment preventive maintenance, calibration, checks and verification Ability to perform microbiological swabbing and air monitoring (e.g. environment program for the micro lab) Ability to work alone and as part of a team to ensure the department goals, accuracy, and timeliness and cost effectiveness are met Show competency through successful completion of proficiency testing MINIMUM QUALIFICATIONS: Associate degree is required or bachelor's degree in one of the following areas: Food Science, Microbiology, Chemistry, Biochemistry or related areas. Equivalent experience in a related field can be substituted for education Math skills combined with the ability to perform and understand scientific based tests and results Ability to communicate effectively in oral and written forms Knowledge of computer applications such as Microsoft Office Excel, Word, etc. Communicate and interact well with others in the laboratory and manufacturing environment Ability to work with minimal supervision and apply Good Laboratory Practices Valid Driver's License PREFERRED QUALIFICATIONS: Some experience in Microbiology/Chemistry lab in the food-processing environment PHYSICAL DEMANDS & ENVIRONMENTAL HAZARDS: The work environment for this position will be typical of the manufacturing facility. There are portions of the job that will require working in cold (< 40°ree;F) environments, in warm environments (>90°ree;F), and loud environments. Must be able to work in a wet, cold, or hot environment Must be able to lift up to 50lbs HOURS & WORKDAYS: 2nd shift, workdays will vary, 2:00pm - 10:30pm & 4:00pm - 12:30am when business requires overtime and weekends will be mandatory. WHAT WE OFFER plus more ! Our rich benefits packages are designed to support the health and well-being of both our eligible team members and families. Medical, Dental & Vision Group Life and AD&D Voluntary Life and AD&D Group Short & Long-Term Disability 401(k) Paid Time Off Flexible Spending Accounts Employee Assistance Program Gym Membership Discounts EQUAL EMPLOYMENT OPPORTUNITY We are an equal opportunity employer committed to fostering a culturally diverse organization. We strive for inclusiveness and a workplace where mutual respect is paramount. We encourage applications from a diverse pool of candidates, and all qualified applicants will receive consideration for employment without regard to race, color, ethnicity, religion, sex, age, national origin, disability, sexual orientation, gender identity and expression, or veteran status. We will provide reasonable accommodation for qualified individuals with disabilities, as needed, to assist them in performing essential job functions. REASONABLE ACCOMMODATIONS Reasonable accommodations will be made to enable individuals with disabilities to perform the essential functions. If you are interested in applying for employment with Generous Brands and need special assistance to apply for a posted position, or if you believe you do not meet any of the required qualifications of a posted position due to a protected disability and would like to explore the possibility of an accommodation, please contact our Talent Acquisition team at *******************************. RECRUITMENT AGENCIES: Confidential does not accept unsolicited agency resumes. Generous Brands is not responsible for any fees related to unsolicited resumes. 2nd shift, workdays will vary, 2:00pm - 10:30pm & 4:00pm - 12:30am when business requires overtime and weekends will be mandatory.

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.

We are hiring a Powder Formulation Technician. The Powder Formulation Technician will be responsible for formulation of powdered media. 3rd Shift: 9:00 pm- 5:30 am At FUJIFILM Irvine Scientific (dba FUJIFILM Biosciences), we turn curiosity into breakthroughs that advance the field of life sciences. By offering a comprehensive portfolio of products and services in cell culture media, discovery research reagents, recombinant growth factors and proteins, fine chemicals, and critical assay materials, we partner with the brightest minds in biotech and pharma to tackle the world's biggest health challenges. Imagine being part of a team that enables life-changing discoveries like new vaccines, therapies, and advancements in regenerative medicine. Our culture fosters curiosity, collaboration, and innovation, and we pride ourselves on delivering unparalleled quality and service to our partners. If you're ready to make an impact, your future belongs with us at FUJIFILM Irvine Scientific (dba FUJIFILM Biosciences). Our headquarters in Santa Ana, California, is surrounded by world-class schools, lush parks, and scenic beaches like Laguna and Huntington, making it an ideal place to live, work, and explore. With additional campuses across the US, Europe, China, and Japan, we offer opportunities to make a difference worldwide. Fujifilm is globally headquartered in Tokyo with over 70,000 employees across four key business segments of healthcare, electronics, business innovation, and imaging. We are guided and united by our Group Purpose of “giving our world more smiles.” Visit: *************************************************** Job Description Responsibilities: Formulates Powder media formulas per manufacturing protocols utilizing various weighing equipment such as scales and balance. Uses Mettler-Toledo IND780 terminal system in conjunction with the SAP ERP system to ensure correct raw materials assigned in the batch record are weighed at the specified quantity. Suggest changes in departmental procedures and processes (SOPs) as needed. Performs and documents line clearance at the start of each formulation event. Maintains all required logs and associated documentation. Assures that all chemicals are stored and labeled properly. Performs process scale checks on all required equipment including scales and balances. Keeps work area, utensils, tanks, mills, and equipment clean and organized. Ensures that supplies needed such as weigh boats, gloves, lab coats, etc. are well stocked in their designated areas. Orders supplies or informs Lead/Supervisor if supplies need to be ordered. Follows all safety procedures and works in a safe manner including wearing all required personal protective equipment. Understands and follows procedures to ensure that chemicals are handled properly. Good understanding of metric system and its conversions. Follows and actively participates in sustaining the 6S program in the area. Other duties as requested by Lead or Supervisor. Required Skills/Education: High School Diploma or equivalent. Background in medical devices, diagnostics, food/vitamin processing, or pharmaceuticals. 1-2 years of hands on experience General education about chemicals and proper handling (college level science preferred). Working knowledge of metric system. Good understanding of current Good Manufacturing Practices (cGMPs). Ability to speak, read, and write English. Good oral and written communication skills. Salary and Benefits: For California, the base salary range for this position is $19.65 - $25.51 per hour. Compensation for the successful candidate will depend on various factors (e.g., qualifications, education, prior experience, location, etc.). Medical, Dental, Vision Life Insurance 401k Paid Time Off *#LI-onsite EEO Information Fujifilm is committed to providing equal opportunities in hiring, promotion and advancement, compensation, benefits, and training regardless of nationality, age, gender, sexual orientation or gender identity, race, ethnicity, religion, political creed, ideology, national, or social origin, disability, veteran status, etc. ADA Information If you require reasonable accommodation in completing this application, interviewing, completing any pre-employment testing, or otherwise participating in the employee selection process, please direct your inquiries to our HR Department (*******************).

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: *****************************************************

Job Details Boulder City, NV Full TimeDescription Armorock is a market leader of precast polymer concrete structures for the wastewater industry. Our mission is to drive the future of sustainable infrastructure with high-quality, innovative solutions that create lasting value. We are dedicated to exceeding customer expectations and fostering a collaborative, rewarding work environment through our QUESST core values: Quality, Unified, Efficient, Safe, Sustainable, Transparent. Position Overview The Quality Inspector is responsible for ensuring that all inventory stored within, and products produced by Armorock meet acceptable quality standards. Day-to-day responsibilities will include, but are not limited to inbound shipment review, outbound product inspection, data entry, report compilation, process observation, inventory review, safety and internal communication. Essential Duties and Responsibilities Service Delivery (80%) Perform pre-pour, post-pour, process, and final inspection of products. Initiate non-conformance reports. Perform receiving inspection and analysis of materials upon receipt. Assist QA Techs in the collection of quality data for analysis. Observe and support standardized manufacturing processes. Enter quality data into the database. Perform other related duties as assigned. Continuous Process Improvement (10%) Maintain SLAs and build a culture of continuous improvement Drive improvement in clarity of process flows and measurement across the organization Collaboration and Research (10%) Collaborate with corporate functions across the board to ensure any required changes to policies, procedures, and processes are implemented Collaborate with data owners/stewards to align on process and data issues Respond to questions and follow up on pertinent escalations Other Duties and Responsibilities Determines how to operationalize processes and improve production quality in alignment with strategic vision Utilizes knowledge of manufacturing operations to drive quality and consistency in operations Uses organizational skills and attention to detail; performs detailed work with speed and accuracy Demonstrates a positive attitude, energy and professionalism Leadership Core Competencies Execution: Sets own goals and ensures others in his/her team achieve goals aligned with business strategy. Building Working Relationships: Develops and builds partnerships with others inside or outside of the company who can provide support. Driving for Results: Sets challenging goals and objectives with clear purpose, direction, and outcomes. Innovation & Creativity: Builds creative solutions to customer and business needs. Essential Leadership Attributes Grounded: Connected to the values of the business; understands service to others/not about own ego. Operating Acumen: Understands varying business models and levers and can use them effectively to build key relationships. Agility/Flexibility: Adapts and executes during changing business conditions, processes, work cultures and environments. Authentic: Places the interests of others and the team ahead of his/her own self interests. Respects and values people and is comfortable living in his/her own skin. Qualifications Position Requirements Education: Bachelor's or associate degree in construction precast manufacturing Experience: 1-3 years' experience in Quality field Certification and Licenses: Familiarity with ISO 9000, NPCA or other certification requirements, preferred Travel Requirements: No major travel requirements Other Key Skills Ability to read blueprints. Ability to use tape measure and other metrology equipment to collect quality data Familiarity and ability to comply with standard quality assurance documentation and operations procedures. Computer literate and detail oriented Ability to work in a fast-paced environment with occasional overtime and weekend work Experience in pre-cast concrete or other heavy industry preferred Familiarity with ISO 9000, NPCA or other certification requirements, preferred Familiarity with lean manufacturing techniques ADA Requirements Environment (office or other): Onsite at manufacturing plant Equipment Operated: Computer, phone, forklift Lifting: Must be able to bend and lift heavy boxes Sitting: Must be able to remain standing and moving 50-75% of the time Management reserves the right to assign or reassign duties and responsibilities on this job at any time. Equal Opportunity Employer - Drug Free Workplace - Background Checks Conducted Why You'll Love Working Here At Armorock, we know that when our employees thrive, our business thrives. That's why we offer top tier benefits that go beyond the basics - because you deserve to feel valued, supported, and empowered in every aspect of your life. Comprehensive medical, dental, and vision insurance with low employee contributions Competitive salary with performance-based bonuses 401(k) with company matching Generous PTO, plus additional sick days Paid parental leave (maternity & paternity) Our Mission and Values At Armorock, our goal is to drive the future of sustainable infrastructure with high-quality, innovative solutions that create lasting value. This mission is possible through our QUESST core values: Quality, Unified, Efficient, Safe, Sustainable, Transparent