Chemist jobs in Redwood City, CA - 182 jobs

AOSense, Inc. is the leading developer and manufacturer of innovative quantum technologies employing atom optics. Our products use frequency-stabilized lasers and atoms in a vacuum cell to measure accelerations, rotations, magnetic fields, and time with unparalleled accuracy and stability. Our staff includes physicists, engineers, and technicians with expertise covering a wide array of disciplines. Our teams are dynamic and fast paced since our hardware is cutting edge. POSITION SUMMARY: We are seeking an R&D technician who specializes in precision assembly and testing. As a hands-on R&D Technician at AOSense, you will work with physicists and engineers to build and test high-performance, fieldable accelerometers, gyroscopes, gravimeters, atomic clocks, frequency standards, and magnetometers, as well as component technologies that we sell commercially to the R&D community. RESPONSIBILITIES: Collaborate with physicists and engineers to assemble and test complex quantum sensor and atomic clock hardware Procure and track inventories of mechanical, optical, vacuum, and electrical components Coordinate component and subsystem fabrication, assembly, and test Assemble precision mechanical systems Align lasers through optical systems Procure and maintain laboratory equipment and supplies Collaborate with engineers to define and implement test plans Bake out and leak test vacuum systems Document and report results of validation testing Requirements Demonstrated success in precision mechanical assembly of prototypes and products Enthusiasm for developing expertise in new fabrication disciplines Proven organizational skills and attention to detail Hands-on experience with test equipment Excellent troubleshooting skills Applicants should thrive in a dynamic environment U.S. Government contracts require applicants to be U.S. citizens or permanent residents DESIRED EXPERIENCE: Expertise aligning and securing micro-optical components Hands-on experience with vacuum system assembly and testing Adept in glovebox assembly work Sensitivity to cleanliness requirements of vacuum and optical assemblies Skilled in mechanical prototyping, including basic machining and finishing operations Practical experience with advanced bonding methods, including soldering, brazing, and adhesives Proficiency with SolidWorks mechanical design software Familiarity with electronics prototyping, including reading schematics, PCB fabrication, assembly, soldering, and rework Experience testing low-noise analog, mixed-signal, and rf electronics Basic knowledge of data acquisition and analysis software such as LabVIEW, MATLAB, and Python EDUCATION AND EXPERIENCE: Associate degree in a relevant technical field or equivalent professional experience, with experience in an R&D environment Benefits Salary depends on qualifications and experience Medical and dental Retirement Stock plan AOSense is an equal opportunity employer (EOE) and considers qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, protected veteran or disability status, or any other federal, state or local protected class. AOSense is committed to providing equal employment opportunity to qualified individuals with disabilities. If you are disabled and require special assistance or a reasonable accommodation while seeking employment with AOSense, then please contact us via email at ******************* or call ************** x210

Join Camb.ai's Speech R&D team to lead innovative speech tech research, integrate findings, and set benchmarks in AI-driven dubbing and Join Camb.ai's pioneering AI team. Lead Speech R&D, integrate tech into products, publish research, and innovate in speech recognition and synthesis. About The Internet was made for English speakers. We are redesigning it for the world. At Camb.ai, we're pioneering the future of AI-driven dubbing, localization, speech synthesis and NMT. Powered by our state-of-the-art models in zero-shot performance transfer and colloquial translation, we're not just innovating; we're setting SOTA benchmarks. Backed by elite global VCs, partnering with enterprise giants and top influencers, guided by an AI leadership with five $100Mn ARR successes, we're seeking top‑tier talent to expand our AI research team comprising of individuals from Carnegie Mellon, Apple and more. Responsibilities Lead and drive innovative research in the field of speech recognition, synthesis, and related technologies. Collaborate closely with the R&D team to integrate research findings into Camb.ai's products. Keep abreast of latest advancements in speech technology and continuously push for innovations in the field. Publish research findings in leading conferences, journals, and workshops. Qualifications PhD or equivalent experience in speech technology, machine learning, or a related field. Proven track record of publishing in leading speech conferences such as Interspeech, ICASSP, etc. Hands‑on experience with popular speech toolkits and frameworks. Strong programming and algorithmic skills. To Apply Please send your resume to *************** with the subject line "Speech R&D Researcher - [Your Name]" in the subject line. Featured Thinking from CAMB.AI Handpicked stories on AI, localization, and reaching audiences worldwide. #J-18808-Ljbffr

A cutting-edge AI startup is seeking an experienced AI Researcher to drive innovative research in generative AI and build multimodal foundation models. Ideally located in San Francisco, the candidate will require a PhD and 5+ years in the field. Responsibilities include designing and implementing models, conducting independent research, and publishing findings. This role is central to advancing AI for earth observation and creating a positive impact. #J-18808-Ljbffr

Title: Lab Pack Chemist Starting Pay: Up to $38/hr depending on experience Contract to Hire - 6 month contract and then direct hire Qualifications: BS degree in science or related with a desire to work in the Environmental industry 2+ years of lab pack experience Great communication and be able to work directly with clients Willing to get their hands dirty and work hard Managers Notes: Will be working for one of their largest clients Will be working between 3 locations and will get paid mileage if they have to go between locations Benefits: Health, Dental and vision insurance 401/k with contribution Tuition Reimbursement Health & Wellness including on location gyms Training, Training, and more Training They have a training schedule/program that everyone does and take 3 years and 120/hrs to complete PTO and Holidays Mentorship and career planning Auto/home insurance discounts Our client, who is one of the largest environmental services firms in North America is looking for Environmental Specialist to join their renowned team of professionals. They provide leading institutions in the higher education, life sciences, healthcare, and industrial sectors with diverse services and advice to assist them with compliance management. As an Environmental Specialist you will support our clients by managing their hazardous waste programs & projects, utilizing state & federal regulations. This is a labor-intensive role that requires a high-level of technical aptitude and the ability to deliver high-level customer service Essential responsibilities and duties: Technical: Completion of on-boarding and Safety Training Development Program Safety equipment inspections Hazardous waste inspections Perform and document environmental health and safety (EHS) audits for clients Regularly preparing chemical and biological waste for shipment and disposal, including creation of all federal/state waste documents and managing the paperwork for the material Following any applicable state and federal regulations [Resource Conservation and Recovery Act (RCRA) & Department of Transportation (DOT) regulations] Develop understanding of OSHA regulations as well as Health and Safety practices Monthly on-call responsibilities as part of our Emergency Response team Hands-on: Material handling (e.g. transportation of materials within client sites as well as from client sites to transfer and/or end disposal facilities) Safe handling of hazardous waste containers on client sites, as well as loading/unloading of waste from vehicles Packaging and prepping of hazardous waste for shipment Spill response measures, including assessment of the spills and potentially leading the cleanup efforts Requires you to work 40+ hours per week and overtime is frequently required Customer service: Professional attitude, high energy, and high-level communication skills required when dealing directly with client representatives High level of expertise (e.g. state/federal regulations, EHS standards, waste management procedures, etc.) Train clients on proper chemical safety and hazardous waste management Attending client operations meetings Training of new team member(s) Qualifications: BS/BA in Environmental Science or Business-related degree or relative Military experience preferred Entry level - recent graduates accepted Valid driver's license Ability to work as a member of a team as well as an individual #LI-JB1

The Opportunity: The Palate of a Chef, the Mind of a Scientist TCHO is looking for a rare professional to serve as the tactical engine of our research and production. This individual will fill a high-impact role that bridges the gap between creative sensory exploration and technical production. This is a hands-on role at our factory, responsible for tending the entire lifecycle of our chocolate. This begins with the cacao beans being grown around the world by our farmer partners, to the final production of high-end chocolate and confections at our production facility in Berkeley. We are seeking a maker who can manage complex data and production schedules while maintaining a disciplined focus on creativity and flavor. This position is 100% onsite due to the hands-on nature of the role, including production, sensory evaluation, laboratory work, and small-batch confectionery manufacturing. 1. Sensory Mastery & Tasting Daily Analysis: Lead disciplined daily sensory panels of raw cacao liquors, experimental batches, finished chocolate, and confections to ensure every product meets TCHO standards. Raw Material Selection: Participate in the selection and sensory analysis of all raw materials, including cocoa beans, liquor, powder, butter, and inclusions such as nuts or vanilla. Final Sign-off: Provide sensory sign-off for final products coming off the line to ensure manufacturing quality and consistency. 2. The “Source” & Laboratory Management Bean Sample Management: Manage the intake of cacao samples from global partners, including roasting, winnowing, and grinding micro-batches to evaluate fermentation quality and genetic potential. Flavor Lab Oversight: Manage daily operations of the flagship TCHO Flavor Lab space (one of only 12 worldwide). Operational Upkeep: Oversee lab organization, cleaning, sample retention, and restocking of laboratory supplies and equipment. 3. Production, Formulation & Retail Confectionery Formula Creation: Develop and manage proprietary daily production formulas used by the manufacturing team. Retail Confectionery Production: Act as a Confectioner for TCHO Retail, responsible for creating small-batch and small-lot confections for retail customers, including hand-crafted and limited-run items. Efficiency & Scalability: Support factory operations by optimizing run times, flush materials, FIFO practices, and small-batch scalability. SOP Compliance: Ensure all product SOPs are followed, including requirements related to cross-contamination, Organic, Kosher, and Fair Trade certifications. 4. New Product Development (NPD) Dream-to-Reality: Translate creative product concepts into consistent, repeatable production. Prototyping: Execute hands-on prototyping and produce sales and retail samples, including chocolate formulas, plant-based ganache, enrobed items, panned goods, and other confections. Scaling: Move products from lab-scale concepts to small industrial and retail-ready production. Who You Are Palate-Driven: You possess an advanced ability to articulate flavor and a deep interest learning how the magic of chocolate comes to life. Analytical: You love a good system and can track R&D data and formulas with precision to keep projects on a professional timeline. Technically Grounded: You likely have a background in Food Science, Pastry, or Confectionery and know your way around the bakery and confectionery world. Onsite & Flexible: This is not a desk job. You are based at our Berkeley HQ and willing to work weekends to keep the lab and production cycles moving. Skills & Abilities Bachelors' degree or equivalent Minimum 3 years working in pastry, confectionary or chocolate industry, Demonstrated leadership experience of teaching and developing teams within food industry. Excellent writing, reading and communication skills Spanish fluency is a major plus. Ability to transport and move 50-pound handloads Must be able to remain in a stationary position for entire shift Must be able to work above ground levels-10 feet and in cold and warm temperature work environment Salary Range - $95,000 - $120,000

We are a group of people united by a strong purpose. We want you to get to know us, and Giuseppe, our very own artificial intelligence. We love good food, but above all, we love the planet, and that's why, to protect it, we reinvent the food industry, one delicious bite at a time, elevating what we eat, through our technology and based on plants. Our recipe has three mega-important components: science, technology, and of course, disruptive talents who work daily to create a better future. At NotCo we are not and do not seek to be the perfect company, but rather the right one. We are here to produce changes, and that is why we dare, fail, and sometimes achieve incredible successes. We are currently looking for a Product Development Scientist for our NotCo B2B Research & Development located in San Francisco, California, requiring an active on-site presence. This position will report to our R&D Sr. Team Lead and the incumbent will work cross-functionally to ensure R&D activities are successfully deployed locally. Responsible for the: Independently conducts day-to-day product development activities as directed by the manager across multiple projects. This includes supporting activities related to the full product lifecycle process (from product concept to successful commercial launch as needed)and supporting process development, scale-up and technology transfer Supports the design and execution of bench-top tests, pilot-plant trials and full-scale formulations to deliver high-quality food products that meet and exceed the sensory, cost, and other performance targets Proactively proposes and uses sensory and analytical analysis to guide and validate the development process Maintains detailed documentation, experiment tracking and outcomes, and documents finished goods and ingredient specifications Provides feedback to project lead regarding relevant technical and process information Communicates proactively and effectively with cross-functional teams, clearly articulating perspectives and trade-offs related to new product development goals Utilizes NotCo's proprietary AI technology to develop and improve food products Supports formula validation activities as well as process development, scale-up and technology transfer Engages in client communications and workshops, bringing technical Maintains detailed documentation across all R&D activities in a timely manner Qualifications / Requirements: Bachelor's degree in Food Engineering, Food Science, Engineering in Biotechnology or a similar discipline. 2 + years of Food R&D experience is desired, preferably across both food and beverage categories. Be agile, adaptable, and thrive in a dynamic and changing culture; works relentlessly to overachieve, anticipate obstacles, and create plans to overcome them. Adapts easily to changing priorities and direction based on new project learnings and team priorities. Demonstrated competency to effectively communicate (oral & written) cross-functionally with solid collaboration skills. Comfortable in client-facing situations and able to communicate complex topics clearly and simply. Excel in a startup environment, is excited to create new procedures and processes from scratch and has a strong entrepreneurial mindset. Be a problem solver, have a general manager mindset, and take the initiative to get the job done Possess strong planning, project management, and execution skills, and the ability to articulate where and how you have used them. Rigorous data-driven/analytical capability and ability and presence to present data effectively to a leadership team Work well in teams and cross-functional groups in a matrixed environment, both regionally and globally Possesses strong computer skills, including a high level of proficiency in MS Office, specifically Excel Authorization to work in the U.S. is required Ability to travel up to 50% of the time, including international travel and extended trips. NotCo is committed to fair and equitable compensation practices. The pay range for this role is $65,000 - $75,000. Actual compensation packages are based on several factors that are unique to each candidate, including but not limited to skill set, depth of experience, certifications, and specific work location. This may be different in other locations due to differences in the cost of labor. We are an equal opportunity employer. All applicants will be considered for employment without attention to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran or disability status.

Job title : QC Specialist - Analytical Development Pay range : $32 - 34/hour on W2 Contract duration : 10-12months This position plays a vital role in advancing analytical capabilities within a dynamic Quality Control Chemistry environment. The successful candidate will be instrumental in implementing cutting-edge analytical methods while ensuring compliance with rigorous pharmaceutical standards. This role demands a detail-oriented professional who can seamlessly balance method development activities with validation protocol execution, all while maintaining meticulous documentation practices. The position requires expertise in operating sophisticated analytical instrumentation and the ability to troubleshoot complex technical challenges. Working collaboratively across multiple functions, this individual will contribute directly to ensuring product quality and regulatory compliance in a fast-paced pharmaceutical setting. Responsibilities: • Support the implementation and integration of new analytical methods within the Quality Control Chemistry department • Maintain comprehensive logs, notebooks, and electronic documentation systems in accordance with regulatory requirements • Conduct method feasibility studies and method development activities to support analytical testing needs • Execute laboratory assays for method validation protocols utilizing various chemistry instrumentation • Operate and maintain analytical equipment including HPLC, UPLC, KF Titrator, Autotitrator, Melting Point meter, Chloride meter, and Polarimeter • Troubleshoot assays and analytical instrumentation to ensure optimal method performance and data quality • Prepare samples using wet chemistry techniques and various analytical methodologies • Generate comprehensive method development reports and method validation reports • Follow established SOPs, pharmacopoeial guidelines, regulatory requirements, and safety protocols • Manage multiple concurrent tasks while working effectively with technical leads across different projects • Interface and collaborate with manufacturing, research, and other cross-functional teams • Utilize LIMS, SAP, and chromatographic software systems for data management and analysis Skills: • Thorough knowledge of chromatography techniques including SEC, ION, NORMAL, REVERSE, and ION-PAIR chromatography • Proficiency in electrophoresis methods including PAGE and agarose gel electrophoresis • Expertise in simple chemistry methods such as spectrophotometry • Strong understanding of biologics and pharmaceutical manufacturing processes • Hands-on experience with LIMS, SAP, and EMPOWER chromatographic software • Comprehensive knowledge of GDP and GMP practices • Excellent documentation and technical writing abilities • Strong analytical and troubleshooting capabilities • Ability to manage multiple priorities and work independently • Effective communication and interpersonal skills for cross-functional collaboration Previous Experience: • Minimum 6 years of experience in pharmaceutical or related industry with a Bachelor's degree, OR • Minimum 2 years of experience with a Master's degree, OR • PhD with relevant pharmaceutical industry exposure • Minimum 3 years of experience in Quality Control laboratory operations • Demonstrated hands-on experience with analytical instrumentation in a regulated environment Qualifications: • Bachelor's degree in Chemistry, Biochemistry, Pharmaceutical Sciences, or related scientific field required • Master's degree or PhD in a relevant scientific discipline preferred Dexian is a leading provider of staffing, IT, and workforce solutions with over 12,000 employees and 70 locations worldwide. As one of the largest IT staffing companies and the 2nd largest minority-owned staffing company in the U.S., Dexian was formed in 2023 through the merger of DISYS and Signature Consultants. Combining the best elements of its core companies, Dexian's platform connects talent, technology, and organizations to produce game-changing results that help everyone achieve their ambitions and goals. Dexian's brands include Dexian DISYS, Dexian Signature Consultants, Dexian Government Solutions, Dexian Talent Development and Dexian IT Solutions. Visit ******************* to learn more. Dexian is an Equal Opportunity Employer that recruits and hires qualified candidates without regard to race, religion, sex, sexual orientation, gender identity, age, national origin, ancestry, citizenship, disability, or veteran status

A construction safety company based in California is seeking a Traffic Control Associate responsible for managing traffic around work zones. Applicants must possess a valid California Driver's License and demonstrate strong interpersonal skills. The position involves coordinating traffic flow, setting up safety equipment, and ensuring the safety of all personnel involved. Potential candidates should have a high school diploma and experience in a similar role is preferred. We offer competitive wages and a robust benefits package. #J-18808-Ljbffr

Medical Device R&D Technician Pay $35-38 6 month+ assignment Onsite in Campbell, CA Assemble fluidic tube sets, mechanical gear, and catheter-based devices in a clean room environment through adhesive bonding and cure, mechatronic assembly and electrical/mechanical testing. Demonstrated history of working on complex mechanical and electrical systems. • HS diploma and a minimum of 8 years related experience; AA degree and a minimum of 5 years experience preferred. • Strong understanding of assembly and calibration methods. • A proven ability to work well in a team environment • Must be capable of working independently and in a team while being flexible and self-motivated. • Previous experience assembling Medical Devices in an FDA-regulated environment is preferred. ESSENTIAL DUTIES AND RESPONSIBILITIES: • Assemble complex mechanical systems that encompass hundreds of unique parts. Your expertise with precision tools will ensure the accurate placement of linear guides, rotary bearings, actuators, motors, and drive systems. • Collaborate closely with engineers to develop work instructions, maintain inventory for development builds, and ensure a clean and organized build environment. • Maintain and calibrate tools, replenish stock fasteners, and ensure organization in the development and build areas. • Actively promote and support the Quality Management System, Quality Objectives, and Quality Policy. • Assure that you and functional subordinates (if applicable) are trained on all applicable procedures and processes according to Good Manufacturing Practices, and applicable FDA and Regulatory requirements. • Actively promote and support the company's Management Review process. • Inform responsible personnel of concerns involving product quality. Benefits (employee contribution): Health insurance Health savings account Dental insurance Vision insurance Flexible spending accounts Life insurance Retirement plan All qualified applicants will receive consideration for employment without regard to age, race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.

JSR Micro is seeking a skilled Analytical Chemist with 3-6 years of experience in a laboratory or Quality Control environment. The ideal candidate will have a solid foundation in trace metals analysis, chromatography, spectroscopy, and wet chemistry techniques, along with proven capabilities in tool management, method development, and data analysis This role requires strong collaboration across teams to support tool qualification, continuous improvement initiatives, and vendor interaction. Candidates must bring excellent problem-solving abilities, proficiency in statistical tools like JMP, and effective communication skills. Familiarity with semiconductor manufacturing, photoresist chemistry, and industry standards such as ISO 17025 or GMP is a plus. If you are a motivated team player who thrives in a fast-paced, quality-driven environment, we invite you to apply. What You'll Do: You will contribute to key lab and process operations by applying your technical expertise, problem-solving skills, and collaborative mindset. In this role, you will: 1. Problem Solving & Decision Making Apply structured problem-solving methods (e.g., DOE, 8D, fishbone analysis, tool partitioning) to resolve QC tool and process issues Operate QC tools and systems (e.g., metrology, PCS, MCC, LIMS) with minimal to moderate supervision Conduct QC test operations and apply statistical analysis using JMP, Excel, Visio, and PowerPoint 2. Teamwork & Collaboration Support projects involving tool installation, qualification, and process or quality improvements (e.g., EH&S or 5S initiatives) Collaborate with vendors to address tool or consumable material issues and support improvement activities Assist QC operations as needed, working as a reliable team member in cross-functional settings 3. Communication Present findings and updates in internal forums such as PCS, MRB, or PCB, and to external vendors Clearly communicate technical concepts and influence team members on topics such as test methodology, metrology performance, LIMS use, process optimization, and troubleshooting 4 . Quality, Creativity & Customer Focus Demonstrate quality awareness in method development, tool qualification, and troubleshooting Apply creative thinking to develop innovative solutions Integrate customer feedback and requirements into testing, proposals, and process improvements 5. Additional Responsibilities Proactively suggest improvements to job functions and lab processes Troubleshoot and support customer resist-related issues Maintain a safe working environment by following safety rules and reporting any unsafe conditions Perform other related duties as assigned What You Bring: 3-6 years of experience as an analytical chemist in a laboratory or R&D environment Demonstrated competency in tool management and/or method development using one or more analytical techniques, such as: Gas, liquid, or ion chromatography Spectroscopy methods (e.g., UV-VIS, IR/NIR) Trace metals analysis using ICP-MS Self-sufficiency in wet lab techniques, including titration and physical property testing Working knowledge of measurement system analysis, statistical quality control (SQC), and laboratory information management systems (LIMS) Proficiency in computer tools such as Excel, Word, PowerPoint, databases, and JMP statistical software Proven problem-solving skills in areas such as tool and process troubleshooting, with minimal to moderate supervision Experience supporting tool installation, qualification, and continuous improvement projects Strong collaboration skills, with the ability to support operations, vendor relationships, and project teams Effective interpersonal and communication skills, including presentations and team influence Preferred: Knowledge of semiconductor manufacturing processes and/or photoresist chemistry Preferred: Familiarity with lab quality standards and practices (e.g., ISO 17025, BKM, GMP) Your Core Strengths: Communication - Clear, concise, and confident in both written and verbal communication; able to effectively present technical information and influence team members and stakeholders Teamwork - A reliable and collaborative team player who contributes meaningfully to cross-functional projects and supports shared goals Problem Solving & Decision Making - Applies analytical thinking and structured problem-solving techniques to address technical challenges and make informed decisions Quality, Creativity & Customer Focus - Committed to delivering high-quality results, bringing innovative ideas to solve problems, and aligning solutions with customer needs and expectations Why Join Us? Innovative Environment - Work in a dynamic Quality Control setting where your contributions directly impact product quality, technology development, and customer satisfaction Professional Growth - Gain hands-on experience with advanced analytical tools, continuous improvement projects, and cross-functional collaboration Supportive Culture - Join a team that values open communication, teamwork, and knowledge sharing, with leaders who invest in your development Meaningful Work - Be part of a company that prioritizes quality, safety, and customer focus-where your work matters and is recognized Industry Relevance - Work on cutting-edge materials and technologies in sectors such as semiconductors, chemical engineering, or advanced materials science Salary Range: $87,000 - $131,000 (Based on skills, experience, and location) Equal Opportunity Employer JSR is an Equal Employment Opportunity and Affirmative Action Employer. We consider all qualified applicants without regard to race, color, religion, sex, sexual orientation, gender identity or expression, national origin, age, marital status, veteran status, or disability status. Third-Party Agencies Recruitment agencies or headhunters: Please do not submit resumes/CVs through our website or directly to managers. JSR does not accept unsolicited resumes from agencies without a signed agreement and will not pay fees for such submissions. #jsrmicro

About AllAccem AllAccem, Inc., founded in 2005, is a medical device and pharmaceutical company focused exclusively on developing and manufacturing products for veterinary healthcare. We manufacture, market, and sell professional veterinary products globally. AllAccem operates as a standalone entity within the Vimian Group. While part of the broader Vimian family-alongside companies such as Movora-AllAccem functions independently with its own products, manufacturing operations, and organizational culture. This role is fully embedded within the AllAccem team and supports on-site manufacturing operations in San Carlos, CA. Position Summary The Associate Chemist is a hands-on role supporting routine chemical manufacturing operations under established standard operating procedures (SOPs). This position is well suited for individuals early in their professional careers or those transitioning into an industrial manufacturing environment who are seeking to build practical experience in regulated production settings. The Associate Chemist works under the guidance of senior chemists and contributes to the reliable execution of production activities, documentation, and equipment preparation. Salary $75-95K DOE Key Responsibilities Manufacturing & Production Support Execute assigned chemical synthesis, purification, and isolation steps in accordance with approved SOPs and batch records. Support multi-kilogram scale production activities through accurate execution of defined procedures. Assist with preparation of reagents, starting materials, and production areas for scheduled manufacturing runs. Documentation, Quality & Compliance Accurately record production data and observations in batch records and associated logs. Follow all quality system requirements, safety procedures, and cleanroom or controlled area practices. Escalate deviations, equipment issues, or safety concerns to senior staff or supervision. Equipment, Housekeeping & Safety Clean, maintain, and stage glassware, tools, and production equipment for daily operations. Assist with setup and teardown of manufacturing equipment, including inert-atmosphere systems. Maintain a clean, organized, and inspection-ready work environment. Requirements BA or BS in Chemistry or a closely related scientific discipline. Academic or internship experience with organic synthesis and basic purification techniques. Familiarity with laboratory safety practices and chemical handling. Ability to lift up to 30 lbs and stand for extended periods. Preferred Qualifications Exposure to industrial, manufacturing, or regulated laboratory environments (internships, co-ops, or entry-level roles). Introductory experience with SOPs, batch records, or quality-controlled documentation. Basic familiarity with inert-atmosphere techniques (e.g., glovebox or Schlenk line) through coursework or research. Knowledge, Skills & Abilities Strong attention to detail and willingness to follow written procedures precisely. Good manual dexterity and hand-eye coordination. Ability to learn new processes quickly in a production-focused environment. Clear communication skills and ability to work effectively as part of a team. Equal Opportunity Employer Statement AllAccem, Inc. is an Equal Opportunity Employer. We are committed to creating an inclusive environment for all employees. All employment is decided on the basis of qualifications, merit, and business need. We do not discriminate based on race, color, religion, creed, sex (including pregnancy, childbirth, breastfeeding, or related medical conditions), sexual orientation, gender, gender identity, gender expression, national origin, ancestry, age (40 and over), disability (mental and physical), genetic information, marital status, military or veteran status, or any other basis protected by federal, state, or local law. Pursuant to the California Equal Pay Act, AllAccem, Inc. does not ask about or consider current or past compensation when determining an applicant's salary. Pay will be based on the job-related skills, experience, and education of the selected candidate. We are also committed to providing reasonable accommodations for qualified individuals with disabilities and disabled veterans in our job application procedures. We actively encourage candidates from all backgrounds to apply for our positions. We believe that a diverse workforce enhances the quality and innovation of our work. Join us in fostering an environment that promotes equal opportunities and celebrates diversity. If you need assistance and/or a reasonable accommodation in the application or recruiting process, please contact ************* Salary Description $75-95k

About AllAccem AllAccem, Inc., founded in 2005, is a medical device and pharmaceutical company focused exclusively on developing and manufacturing products for veterinary healthcare. We manufacture, market, and sell professional veterinary products globally. AllAccem operates as a standalone entity within the Vimian Group. While part of the broader Vimian family-alongside companies such as Movora-AllAccem functions independently with its own products, manufacturing operations, and organizational culture. This role is fully embedded within the AllAccem team and supports on-site manufacturing operations in San Carlos, CA. Position Summary The Associate Chemist is a hands-on role supporting routine chemical manufacturing operations under established standard operating procedures (SOPs). This position is well suited for individuals early in their professional careers or those transitioning into an industrial manufacturing environment who are seeking to build practical experience in regulated production settings. The Associate Chemist works under the guidance of senior chemists and contributes to the reliable execution of production activities, documentation, and equipment preparation. Salary $75-95K DOE Key Responsibilities Manufacturing & Production Support * Execute assigned chemical synthesis, purification, and isolation steps in accordance with approved SOPs and batch records. * Support multi-kilogram scale production activities through accurate execution of defined procedures. * Assist with preparation of reagents, starting materials, and production areas for scheduled manufacturing runs. Documentation, Quality & Compliance * Accurately record production data and observations in batch records and associated logs. * Follow all quality system requirements, safety procedures, and cleanroom or controlled area practices. * Escalate deviations, equipment issues, or safety concerns to senior staff or supervision. Equipment, Housekeeping & Safety * Clean, maintain, and stage glassware, tools, and production equipment for daily operations. * Assist with setup and teardown of manufacturing equipment, including inert-atmosphere systems. * Maintain a clean, organized, and inspection-ready work environment. Requirements * BA or BS in Chemistry or a closely related scientific discipline. * Academic or internship experience with organic synthesis and basic purification techniques. * Familiarity with laboratory safety practices and chemical handling. * Ability to lift up to 30 lbs and stand for extended periods. Preferred Qualifications * Exposure to industrial, manufacturing, or regulated laboratory environments (internships, co-ops, or entry-level roles). * Introductory experience with SOPs, batch records, or quality-controlled documentation. * Basic familiarity with inert-atmosphere techniques (e.g., glovebox or Schlenk line) through coursework or research. Knowledge, Skills & Abilities * Strong attention to detail and willingness to follow written procedures precisely. * Good manual dexterity and hand-eye coordination. * Ability to learn new processes quickly in a production-focused environment. * Clear communication skills and ability to work effectively as part of a team. Equal Opportunity Employer Statement AllAccem, Inc. is an Equal Opportunity Employer. We are committed to creating an inclusive environment for all employees. All employment is decided on the basis of qualifications, merit, and business need. We do not discriminate based on race, color, religion, creed, sex (including pregnancy, childbirth, breastfeeding, or related medical conditions), sexual orientation, gender, gender identity, gender expression, national origin, ancestry, age (40 and over), disability (mental and physical), genetic information, marital status, military or veteran status, or any other basis protected by federal, state, or local law. Pursuant to the California Equal Pay Act, AllAccem, Inc. does not ask about or consider current or past compensation when determining an applicant's salary. Pay will be based on the job-related skills, experience, and education of the selected candidate. We are also committed to providing reasonable accommodations for qualified individuals with disabilities and disabled veterans in our job application procedures. We actively encourage candidates from all backgrounds to apply for our positions. We believe that a diverse workforce enhances the quality and innovation of our work. Join us in fostering an environment that promotes equal opportunities and celebrates diversity. If you need assistance and/or a reasonable accommodation in the application or recruiting process, please contact ************* Salary Description $75-95k

Clean Earth is a leading provider of environmental services in the United States providing remediation, disposal, recycling, and beneficial reuse solutions for hazardous and non-hazardous waste, contaminated soil, and dredged material. Our vast portfolio of technologies and services touches nearly every industry that generates waste including energy, infrastructure, commercial, industrial, retail, and healthcare markets. Every day our teams across the country take a hands-on, dedicated approach to recycling and beneficially reusing waste that would otherwise go into landfills. We value our employees as our most important asset, and this is reflected in many areas across our company including recently being named a 2024 Most Loved Workplace . We are committed to creating a positive work culture that fosters growth and development while ensuring the health and safety of our employees. Why join Clean Earth? In addition to competitive pay, we also offer: Health benefits available Day 1 401k available Day 1 10+ paid holidays/year Free HAZWOPER training and certification Overtime opportunities Ability to be cross-trained into different roles Job Description PRINCIPAL DUTIES AND RESPONSIBILITIES: Handles hazardous materials including inventorying, identifying, segregating, and packaging waste material in accordance with Lab Pack policies, procedures and practices and all applicable regulations. Perform onsite services which may include waste collection, consolidation (i.e., bulking, repackaging), sampling, safety/compliance inspections, and other related activities required by the customer/contract. Assists other business groups, i.e., Depack, Retail and HHW, both internal and onsite as needed. Preparing shipment of packaged waste by inspecting, labeling, marking, and loading into the transport vehicle. Properly completes documentation including shipping papers, Land Disposal Restrictions (LDR's), evaluations/certifications and other required documentation in accordance with appropriate regulations and procedures. Maintain a Commercial Driver's License (CDL) with Hazmat Endorsement to legally operate Clean Earth vehicles necessary for transporting personnel and waste to and from customers' job locations. Follows, understands, and promotes by example, all Health & Safety /Job Safety Analysis (JSA's) procedures including development of on-site Health &Safety plans/JSA's as outlined in the procedures and policies. Perform unknown field testing for classification and packaging for transportation and disposal. Mentor and assist new employees in field work duties. Complete site walks to inventory and assess requirements for potential and awarded work. Assist sales in creating estimates for lab pack work. Lead/coordinate field service/lab pack jobs requiring multiple personnel/days. Assist in other areas as directed including but not limited to assistance in scheduling and support of staff training. Performs other duties as assigned Starting pay $38.00 hourly. Qualifications Basic Requirements: Associate College in general science (BS preferred) is required for the Lab Pack Chemist. Commercial Driver's License (CDL) with Hazardous Material endorsement and a clear record Moderate to extensive travel with 20% overnight travel Physical ability to lift and move material of various weights frequently exceeding 55 lbs Basic understanding of chemistry through general chemistry or biology Advanced knowledge of EPA and DOT Minimum two (2) years lab pack experience 40-hour OSHA HAZWOPER 8 hours DOT Training PPE Training which includes Respirators 40 hours Depack Experience This position requires a CDL B to be obtained within a 6-month period from your start date. Failure to obtain a CDL B within the 6-month period will mean you are no longer eligible for the Lab Pack Chemist position. This position is also contingent upon successful completion of a DOT physical, DOT Drug Screen and any other DOL or company requirements. Additional Information Clean Earth offers competitive benefits including health, dental, vision, life, and disability insurance plans starting on the first day of employment; paid time off, wellness benefits, employee discount program, tuition assistance, and a 401k with company matching. We provide equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, sex, national origin, age, disability, veteran status, gender identity, or genetics. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation, and training. If you have a difficulty applying for any job posted on Enviri Clean Earth's website because a disability prevents you from using the online system, Clean Earth offers the following alternate application procedure: Call toll free ************** and leave your name, phone number, city and state of residence. Clean Earth will arrange for an alternate method of applying and will consider your application together with all other applications received for the job. This line is dedicated to disability applications only. No other inquiries will receive a response. Military veterans encouraged to apply

Pharma Aerogen Pharma is a US based clinical-stage specialty pharmaceutical company with a mission to develop inhaled drug/biologic and device combination that will transform the standard of care for acute and critically ill patients. Our goal is to create medically superior, proprietary and commercially differentiated combination products by combining proven therapeutic molecules with a unique, high-performance aerosol delivery system. We are embarking on an exciting and dynamic stage in our combination product development, moving into phase 3 clinical trial for one of the biggest breakthroughs in Neonatal care. We are a team of passionate industry experts who are leading, shaping, and driving a potentially transformative medical breakthrough for the treatment of neonatal respiratory distress syndrome (RDS) in the developed world. Additionally, in partnership with The Bill & Melinda Gates Foundation, we have an ambitious program in development to bring low-cost surfactant to the millions of premature babies with RDS born each year. Join us as we embark on this breakthrough and become inspired to deliver. What is the role? The person in this role will develop analytical techniques and conduct experiments to support the development of commercially viable lipid-peptide and lipid-protein formulations. In addition, the person will support formulation development efforts. This role is crucial for advancing our CMC program for the Gates project, as well as establishing analytical capabilities and in expertise in our expanding portfolio, ensuring products meet rigorous quality and regulatory standards. The person will be hands on in the lab with strong technical knowledge in analytical science and will be mentored to assist in formulation development efforts. What are the key responsibilities? Analytical chemistry: Develop and optimization analytical methods for characterizing and controlling the quality the quality attributes of lipid-peptide and lipid-protein formulations. Support formulation development and design of experiment studies. Formulation science: Support formulation development efforts by participating in formulation runs with guidance form formulation science staff. Regulatory Compliance: Prepare and review documentation describing development efforts for regulatory submissions (INDs, BLAs, NDAs) Cross-Functional Collaboration: Work closely with formulation scientists and laboratory management staff, to integrate analytical development within overall project goals. Troubleshooting & Problem Solving: Address and resolve complex analytical issues during development and manufacturing. Continuous Improvement: Stay updated on advancements in analytical techniques and industry trends. What Education and Experience are required? A degree in Chemistry, Analytical chemistry, Biochemistry or related field. 2-5 years of experience in analytical development or quality control. Experience in lipid formulations, liposomes, or related drug delivery technologies, including homogenization and lyophilization is a plus. Experience in technical writing is required. Authoring CMC dossiers for FDA, EMA, and other regulatory agencies is a plus. Knowledge and experience in drug-device development, inhalation drug delivery is a plus. Excellent written and oral communication skills. What key skills will make you great at the role? Technical expertise: Proficiency in analytical techniques such as UHPLC, mass spectrometry and CAD as they apply to lipid characterization methods. Experience with drug-device combination products is a plus. Understanding of laboratory procedures, equipment, software, and data analysis. Data-driven decisions: Use lab data to make informed decisions about operations, budget, and performance. Problem-solving and strategic thinking: Quickly and effectively address challenges, from equipment malfunctions to staffing issues. Develop clear strategies and plans to achieve the lab's objectives. Collaboration and adaptability: Foster a collaborative environment where teams can work together seamlessly. Work well under pressure and adapt to changing priorities in a fast-paced environment. Compliance and safety: Ensure a safe and complaint work environment. Training, procedures, quality: Ensure up to date training on procedures and best practices. Ensure the lab meets all relevant quality standards and documentation requirements. Why Aerogen Pharma? As a key member of Aerogen Group, the global market leader in high performance aerosol drug delivery, Aerogen Pharma is at a pivotal point in the company's life cycle. With plans to expand and centralize our US hubs over the next two years, we offer an environment where you can thrive professionally and learn from driven industry leaders in drug development and commercialization, inhaled devices, and neonatology. We foster an inclusive culture that empowers you to contribute to the transformation of Neonatal care, where potential is recognized, and professional development is encouraged.

CDL Sign-on Bonus: $3,000 Clean Earth is a leading provider of environmental services in the United States providing remediation, disposal, recycling, and beneficial reuse solutions for hazardous and non-hazardous waste, contaminated soil, and dredged material. Our vast portfolio of technologies and services touches nearly every industry that generates waste including energy, infrastructure, commercial, industrial, retail, and healthcare markets. Every day our teams across the country take a hands-on, dedicated approach to recycling and beneficially reusing waste that would otherwise go into landfills. We value our employees as our most important asset, and this is reflected in many areas across our company including recently being named a 2024 Most Loved Workplace . We are committed to creating a positive work culture that fosters growth and development while ensuring the health and safety of our employees. Why join Clean Earth? In addition to competitive pay, we also offer: Health benefits available Day 1 401k available Day 1 10+ paid holidays/year Free HAZWOPER training and certification Overtime opportunities Ability to be cross-trained into different roles Job Description PRINCIPAL DUTIES AND RESPONSIBILITIES: Handles hazardous materials including inventorying, identifying, segregating, and packaging waste material in accordance with Lab Pack policies, procedures and practices and all applicable regulations. Perform onsite services which may include waste collection, consolidation (i.e., bulking, repackaging), sampling, safety/compliance inspections, and other related activities required by the customer/contract. Assists other business groups, i.e., Depack, Retail and HHW, for both internally and onsite as needed. • Preparing shipment of packaged waste by inspecting, labeling, marking, and loading into the transport vehicle Properly completes documentation including shipping papers, Land Disposal Restrictions (LDR's), evaluations/certifications and other required documentation in accordance with appropriate regulations and procedures. May require obtaining and maintaining a Commercial Driver's License (CDL) with Hazmat Endorsement to legally operate Clean Earth vehicles necessary for transporting personnel and waste to and from customers' job locations. Follows, understands, and promotes by example, all Health & Safety /Job Safety Analysis (JSA's) procedures including development of on-site Health &Safety plans/JSA's as outlined in the procedures and policies. Performs other duties as assigned. Starting pay $33.00 hourly. Qualifications Basic Requirements: An associate's degree in general science (BS preferred) is required for the Lab Pack Chemist. Driver's License with clear record Moderate to extensive travel with 20% overnight travel Physical ability to lift and move material of various weights frequently exceeding 55 lbs. Basic understanding of chemistry through general chemistry or biology This position requires a CDL B to be obtained within a 6-month period from your start date. Failure to obtain a CDL B within the 6-month period will mean you are no longer eligible for the Lab Pack Chemist position. This position is also contingent upon successful completion of a DOT physical, DOT Drug Screen and any other DOL or company requirements. Additional Information Clean Earth offers competitive benefits including health, dental, vision, life, and disability insurance plans starting on the first day of employment; paid time off, wellness benefits, employee discount program, tuition assistance, and a 401k with company matching. We provide equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, sex, national origin, age, disability, veteran status, gender identity, or genetics. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation, and training. If you have a difficulty applying for any job posted on Enviri Clean Earth's website because a disability prevents you from using the online system, Clean Earth offers the following alternate application procedure: Call toll free ************** and leave your name, phone number, city and state of residence. Clean Earth will arrange for an alternate method of applying and will consider your application together with all other applications received for the job. This line is dedicated to disability applications only. No other inquiries will receive a response. Military veterans encouraged to apply

Shift: Monday -Friday 2: 00 PM -10: 30 PM with overtime and weekend hours as needed Duration: 12 Months Pay range: $25.30 Hourly - $25.30 Hourly Onsite Job How Will You Make an Impact? Work in a team-based environment within a manufacturing lab responsible for synthesizing and testing ion exchange media used in chromatography consumables. A Day in the Life: •Testing of 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 policy to ensure high-quality standards. •Follow safety requirements and actively participate in safety improvement activities! •Maintain a clean and organized laboratory environment. Education: High school diploma or equivalent required. Experience: •Required: No previous work experience required •Preferred: Previous work experience in manufacturing, operations, production or lab setting or related field Knowledge, Skills, Abilities: •Knowledge of Good Laboratory and Manufacturing Practices and standards. •Good mathematical, problem-solving, and organizational abilities. •Excellent verbal and written skills •Ability to read and understand written procedures (SOPs) and follow verbal instructions. •Familiarity with hand tools regularly used (wrenches, torque drivers, tweezer, etc.) •PC literate and have experience with spreadsheet and database software. Physical Requirements / Work Environment •Lift and/or move up to 40 pounds. •Regularly required to sit, stand;walk;use hands & fingers to handle & feel. •Visual abilities to detect small components and particles. •Exposure to toxic or caustic chemicals, fumes or airborne particles. •Occasionally exposed to moving mechanical parts and moderate noise level. •PPE requirements: lab coat, Safety glasses, gloves, face shields, & safety shoes (all company provided.) •P95 Mask in the areas that have exposure of solvent fumes 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.

We are a group of people united by a strong purpose. We want you to get to know us, and Giuseppe, our very own artificial intelligence. We love good food, but above all, we love the planet, and that's why, to protect it, we reinvent the food industry, one delicious bite at a time, elevating what we eat, through our technology and based on plants. Our recipe has three mega-important components: science, technology, and of course, disruptive talents who work daily to create a better future. At NotCo we are not and do not seek to be the perfect company, but rather the right one. We are here to produce changes, and that is why we dare, fail, and sometimes achieve incredible successes. We are currently looking for a Product Development Scientist for our NotCo B2B Research & Development located in San Francisco, California, requiring an active on-site presence. This position will report to our R&D Sr. Team Lead and the incumbent will work cross-functionally to ensure R&D activities are successfully deployed locally. Responsible for the: Independently conducts day-to-day product development activities as directed by the manager across multiple projects. This includes supporting activities related to the full product lifecycle process (from product concept to successful commercial launch as needed)and supporting process development, scale-up and technology transfer Supports the design and execution of bench-top tests, pilot-plant trials and full-scale formulations to deliver high-quality food products that meet and exceed the sensory, cost, and other performance targets Proactively proposes and uses sensory and analytical analysis to guide and validate the development process Maintains detailed documentation, experiment tracking and outcomes, and documents finished goods and ingredient specifications Provides feedback to project lead regarding relevant technical and process information Communicates proactively and effectively with cross-functional teams, clearly articulating perspectives and trade-offs related to new product development goals Utilizes NotCo's proprietary AI technology to develop and improve food products Supports formula validation activities as well as process development, scale-up and technology transfer Engages in client communications and workshops, bringing technical Maintains detailed documentation across all R&D activities in a timely manner Qualifications / Requirements: Bachelor's degree in Food Engineering, Food Science, Engineering in Biotechnology or a similar discipline. 2 + years of Food R&D experience is desired, preferably across both food and beverage categories. Be agile, adaptable, and thrive in a dynamic and changing culture; works relentlessly to overachieve, anticipate obstacles, and create plans to overcome them. Adapts easily to changing priorities and direction based on new project learnings and team priorities. Demonstrated competency to effectively communicate (oral & written) cross-functionally with solid collaboration skills. Comfortable in client-facing situations and able to communicate complex topics clearly and simply. Excel in a startup environment, is excited to create new procedures and processes from scratch and has a strong entrepreneurial mindset. Be a problem solver, have a general manager mindset, and take the initiative to get the job done Possess strong planning, project management, and execution skills, and the ability to articulate where and how you have used them. Rigorous data-driven/analytical capability and ability and presence to present data effectively to a leadership team Work well in teams and cross-functional groups in a matrixed environment, both regionally and globally Possesses strong computer skills, including a high level of proficiency in MS Office, specifically Excel Authorization to work in the U.S. is required Ability to travel up to 50% of the time, including international travel and extended trips. NotCo is committed to fair and equitable compensation practices. The pay range for this role is $65,000 - $75,000. Actual compensation packages are based on several factors that are unique to each candidate, including but not limited to skill set, depth of experience, certifications, and specific work location. This may be different in other locations due to differences in the cost of labor. We are an equal opportunity employer. All applicants will be considered for employment without attention to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran or disability status.

CDL Sign-on Bonus: $3,000 Clean Earth is a leading provider of environmental services in the United States providing remediation, disposal, recycling, and beneficial reuse solutions for hazardous and non-hazardous waste, contaminated soil, and dredged material. Our vast portfolio of technologies and services touches nearly every industry that generates waste including energy, infrastructure, commercial, industrial, retail, and healthcare markets. Every day our teams across the country take a hands-on, dedicated approach to recycling and beneficially reusing waste that would otherwise go into landfills. We value our employees as our most important asset, and this is reflected in many areas across our company including recently being named a 2024 Most Loved Workplace . We are committed to creating a positive work culture that fosters growth and development while ensuring the health and safety of our employees. Why join Clean Earth? In addition to competitive pay, we also offer: Health benefits available Day 1 401k available Day 1 10+ paid holidays/year Free HAZWOPER training and certification Overtime opportunities Ability to be cross-trained into different roles Job Description PRINCIPAL DUTIES AND RESPONSIBILITIES: Handles hazardous materials including inventorying, identifying, segregating, and packaging waste material in accordance with Lab Pack policies, procedures and practices and all applicable regulations. Perform onsite services which may include waste collection, consolidation (i.e., bulking, repackaging), sampling, safety/compliance inspections, and other related activities required by the customer/contract. Assists other business groups, i.e., Depack, Retail and HHW, for both internally and onsite as needed. • Preparing shipment of packaged waste by inspecting, labeling, marking, and loading into the transport vehicle Properly completes documentation including shipping papers, Land Disposal Restrictions (LDR's), evaluations/certifications and other required documentation in accordance with appropriate regulations and procedures. May require obtaining and maintaining a Commercial Driver's License (CDL) with Hazmat Endorsement to legally operate Clean Earth vehicles necessary for transporting personnel and waste to and from customers' job locations. Follows, understands, and promotes by example, all Health & Safety /Job Safety Analysis (JSA's) procedures including development of on-site Health &Safety plans/JSA's as outlined in the procedures and policies. Performs other duties as assigned. Starting pay $33.00 hourly. Qualifications Basic Requirements: An associate's degree in general science (BS preferred) is required for the Lab Pack Chemist. Driver's License with clear record Moderate to extensive travel with 20% overnight travel Physical ability to lift and move material of various weights frequently exceeding 55 lbs. Basic understanding of chemistry through general chemistry or biology This position requires a CDL B to be obtained within a 6-month period from your start date. Failure to obtain a CDL B within the 6-month period will mean you are no longer eligible for the Lab Pack Chemist position. This position is also contingent upon successful completion of a DOT physical, DOT Drug Screen and any other DOL or company requirements. Additional Information Clean Earth offers competitive benefits including health, dental, vision, life, and disability insurance plans starting on the first day of employment; paid time off, wellness benefits, employee discount program, tuition assistance, and a 401k with company matching. We provide equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, sex, national origin, age, disability, veteran status, gender identity, or genetics. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation, and training. If you have a difficulty applying for any job posted on Enviri Clean Earth's website because a disability prevents you from using the online system, Clean Earth offers the following alternate application procedure: Call toll free ************** and leave your name, phone number, city and state of residence. Clean Earth will arrange for an alternate method of applying and will consider your application together with all other applications received for the job. This line is dedicated to disability applications only. No other inquiries will receive a response. Military veterans encouraged to apply

Shift: Monday -Friday with overtime and weekend hours as needed Duration: 12 Months Pay range: $23.00 Hourly - $23.00Hourly Onsite Job How Will You Make an Impact? Work in a team-based environment within a manufacturing lab responsible for synthesizing and testing ion exchange media used in chromatography consumables. A Day in the Life: Testing of 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 policy to ensure high-quality standards. Follow safety requirements and actively participate in safety improvement activities! Maintain a clean and organized laboratory environment. Education: High school diploma or equivalent required. Experience: Required: No previous work experience required Preferred: Previous work experience in manufacturing, operations, production or lab setting or related field Knowledge, Skills, Abilities: Knowledge of Good Laboratory and Manufacturing Practices and standards. Good mathematical, problem-solving, and organizational abilities. Excellent verbal and written skills Ability to read and understand written procedures (SOPs) and follow verbal instructions. Familiarity with hand tools regularly used (wrenches, torque drivers, tweezer, etc.) PC literate and have experience with spreadsheet and database software. Physical Requirements / Work Environment Lift and/or move up to 40 pounds. Regularly required to sit, stand;walk;use hands & fingers to handle & feel. Visual abilities to detect small components and particles. Exposure to toxic or caustic chemicals, fumes or airborne particles. Occasionally exposed to moving mechanical parts and moderate noise level. PPE requirements: lab coat, Safety glasses, gloves, face shields, & safety shoes (all company provided.) P95 Mask in the areas that have exposure of solvent fumes. 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.