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The Senior Quality Control Scientist (SQCS) is the primary technical support contact for peers within the Pharmgate Quality Control Laboratories. The SQCS is also responsible for performing their own primary analytical duties, maintaining quality control and assurance of materials and instrumentation used in the laboratory. Additionally, the SQCS will help assure that daily, weekly, and/or monthly workflow tasks are completed to meet company and department goals. The position is key to supporting Laboratory management while independently applying advanced scientific knowledge to projects and assures adherence to Standard Operating Procedures(SOPs), Current Good Manufacturing Practices (cGMP) and other industry and company required standards and policies. Technical Workflow Responsibilities: • Provide guidance on daily tasks for efficient workflow and assignments in the laboratory., • Oversee consistency in training across all areas of the laboratory., • Provide opportunities for on-the-job training and SOP review as necessary., • Troubleshoot and resolve work problems or assist workers in solving work problems., • Communicate difficulties, either production or personnel, with plans for resolution, to management for consultation and resolution approval. Individual Workflow Duties/Responsibilities: • Identify and recommend improvements to processes to maintain quality, cost-effectiveness, safety compliance, and other parameters., • Perform timely release testing on all incoming raw materials needed for manufacturing and finished goods., • Coordinate scheduling of all materials in order to meet company requirements., • Ensure that assigned products meet quality requirements for the customer and the company., • Draft written reports detailing results of testing analysis., • Approve release of raw materials and finished goods., • Proactively identify trends in laboratory analysis or functions and act to make improvements and/or communicate to management., • Perform operations for CMO support as necessary., • Operate and maintain laboratory equipment; identify problems when equipment fails and conduct or recommend repairs., • Perform maintenance and calibration of all equipment as needed., • Perform peer review of analytical results of peers., • Perform peer review of test methods and protocols., • Review and/or draft SOPs as needed to update to current procedures., • Author and execute written protocols and IQOQs as needed., • Cross train to be able to perform sample lab duties adequately and accurately., • Act as Quality Department Representative when necessary., • Perform other duties as assigned. Required Skills/Abilities: • Excellent organizational skills and attention to detail., • Thorough understanding of chemical tests and processes., • Understanding and proficiency in basic laboratory techniques and scientific instrumentation, including direct HPLC experience and troubleshooting., • Ability to follow Standard Operating Procedures (SOPs) and GMP guidelines. Ensure compliance with all NADAs/ANADAs., • Excellent time management skills with a proven ability to meet deadlines., • Strong verbal and written communication skills and the ability to work with all levels of personnel., • Strong analytical and problem-solving skills including the ability to read and understand instructions and materials in English; add, subtract, multiply, and divide in all units of measure, using whole numbers, common fractions, and decimals., • Ability to function well in a high-paced and at times stressful environment., • Thorough understanding of FDA and cGMP compliance regulations., • Proficient with Microsoft Office Suite, virtual meeting applications, SAP Business One, and other related software. Education and Experience: • Bachelor of Science in Chemistry, Microbiology or Biology, required., • 3-5 years of experience in an FDA regulated pharmaceutical laboratory facility or other highly regulated industry, preferred. Physical Requirements: • Prolonged periods of standing and walking., • Exposure to various chemicals and compounds., • Prolonged periods of sitting at a desk working on computers., • Ability to occasionally lift 50 lbs. from floor to waist level., • Ability to occasionally climb stairs.

Job Description Now Hiring: Lab Technician Job Description This role performs rapid microbiological testing on raw and processed meat samples to detect pathogens and indicator organisms, supporting safe, high-quality products and timely release decisions. The lab technician works in a modern, clean laboratory using advanced rapid microbiology methods and equipment while following strict regulatory, quality, and safety standards. Responsibilities • Perform rapid microbiological testing such as PCR, ATP, and immunoassay-based methods on raw and processed meat samples to detect pathogens and indicator organisms., • Receive, label, and process meat samples according to validated methods, standard operating procedures (SOPs), and applicable regulatory requirements, including USDA/FSIS, FDA, and ISO guidelines., • Operate, calibrate, and maintain laboratory instruments and testing equipment used for rapid microbiology analysis to ensure accurate and reliable results., • Accurately document test results, quality control data, and any deviations in the Laboratory Information Management System (LIMS) or other laboratory records., • Follow strict aseptic techniques, biosafety protocols, and sanitation procedures to prevent cross-contamination and ensure sample integrity., • Communicate test results clearly and promptly to supervisors and cross-functional teams to support timely product release and decision-making., • Maintain a clean, organized laboratory workspace and ensure compliance with Good Manufacturing Practices (GMP), Hazard Analysis and Critical Control Points (HACCP), and laboratory safety standards., • Participate in routine quality checks, equipment verifications, and process improvements to enhance testing accuracy and efficiency., • Collaborate with team members to troubleshoot testing issues, share best practices, and support continuous improvement in laboratory operations. Essential Skills • Hands-on experience with microbiology or biology laboratory techniques, including pipetting and routine lab testing., • Ability to perform rapid microbiological methods such as PCR, ATP, and immunoassay-based testing., • Strong attention to detail for accurate sample labeling, handling, and documentation., • Familiarity with aseptic techniques, biosafety practices, and sanitation procedures in a laboratory setting., • Ability to operate, calibrate, and maintain laboratory instruments and testing equipment., • Competence in documenting test results and quality control data in LIMS or laboratory records., • Understanding of or ability to follow regulatory requirements such as USDA/FSIS, FDA, and ISO for laboratory testing., • Knowledge of or ability to comply with GMP, HACCP, and laboratory safety standards., • Effective communication skills to clearly convey results and issues to supervisors and cross-functional teams., • Ability to work scheduled shifts, including afternoons, evenings, and weekends as required. Additional Skills & Qualifications • Associates or Bachelors degree in a science-related field is preferred., • If no degree, at least 1+ years of relevant laboratory experience is required., • Background in biology, microbiology, or a related scientific discipline., • Experience working in a food, meat, or related industry laboratory environment is beneficial., • Comfort working with Laboratory Information Management Systems (LIMS) or similar digital record systems., • Ability to work collaboratively in a small, close-knit team and contribute to a supportive, fun culture., • Interest in contributing to a growing facility that is bringing in new business and impacting the industry in the region. Work Environment The position is based in a new, very clean laboratory equipped with modern, state-of-the-art instruments for rapid microbiology testing. The initial shift runs Tuesday through Saturday from 2:00 p.m. to 10:30 p.m., with a first-shift schedule of Tuesday through Saturday from 10:00 a.m. to 6:30 p.m. The team is small, close, and highly collaborative, with a fun, supportive culture where colleagues help each other regularly. The environment emphasizes safety, organization, and adherence to GMP, HACCP, and laboratory safety standards while providing the opportunity to work with new equipment in a growing facility that is expanding its impact in the Midwest. Job Type & Location This is a Contract to Hire position based out of Omaha, NE. Pay and Benefits The pay range for this position is $19.50 - $19.50/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors. 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 Omaha,NE. Application Deadline This position is anticipated to close on Oct 9, 2026. 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 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service. The company is an equal opportunity employer and will consider all applications withoutregard to race, sex, age, color, religion, national origin, veteran status, disability,sexual orientation, gender identity, genetic information or any characteristic protectedby law. If you would like to request a reasonable accommodation, such as the modification oradjustment of the job application process or interviewing process due to a disability,please email actalentaccommodation@actalentservices.com for other accommodation options. San Francisco Fair Chance Ordinance:Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in thecity and county of San Francisco, we will consider for employment qualified applicantswith arrest and conviction records. Massachusetts Lie Detector:It is unlawful in Massachusetts to require or administer a lie detector test as acondition of employment or continued employment. An employer who violates this lawshall be subject to criminal penalties and civil liability. Use of Artificial Intelligence (AI):We may use Artificial Intelligence (AI) to support parts of our hiring process,including sourcing, screening, and evaluating candidates. AI helps assess applicationsand qualifications, but final decisions are made by our hiring team. By applying, youacknowledge and agree that your application may be reviewed using AI tools.

Job DescriptionOverview We are seeking a detail-oriented Quality Documentation Specialist to support quality assurance activities within a regulated manufacturing environment. This role is responsible for reviewing and approving raw materials, coordinating laboratory testing, maintaining quality documentation, and ensuring compliance with GMP, FDA, and internal quality standards. The ideal candidate will have experience in quality systems, laboratory processes, and regulatory documentation, along with a strong commitment to accuracy and continuous improvement. What You'll Do • Inspect and approve incoming raw materials to ensure compliance with quality standards., • Coordinate and perform raw material sampling and testing activities., • Maintain accurate quality documentation and records in accordance with GMP requirements., • Ensure compliance with Standard Operating Procedures (SOPs) and quality policies., • Coordinate laboratory testing for raw materials, environmental monitoring, food-contact surfaces, and finished products., • Support investigations, corrective actions, and continuous improvement initiatives., • Participate in root cause analysis and CAPA activities to address quality concerns., • Assist with internal and external audits and regulatory compliance efforts., • Collaborate with quality, production, and laboratory teams to drive product quality and process improvements.QualificationsRequired, • Experience in Quality Assurance, Quality Control, or Quality Documentation., • Knowledge of CAPA processes and Root Cause Analysis methodologies., • Strong data entry and documentation skills., • Familiarity with laboratory processes and testing environments., • Understanding of FDA regulations, GMP requirements, and audit processes., • Strong attention to detail and organizational skills.Preferred, • Bachelor's degree in Chemistry, Biology, Food Science, Microbiology, or a related scientific field with 1+ year of GMP experience., • OR Associate's degree in a scientific discipline with 3+ years of quality documentation experience in a GMP-regulated environment., • Experience working in food, pharmaceutical, biotech, or other regulated manufacturing industries.Work Environment, • Monday-Friday schedule, 7:30 AM to 4:00 PM., • Minimal overtime required., • Laboratory and quality-focused work environment., • Strong emphasis on regulatory compliance, documentation accuracy, and product quality., • Collaborative team setting with interaction across quality, laboratory, and production departments.Why Join Us?, • Stable weekday schedule with excellent work-life balance., • Opportunity to work in a highly regulated and quality-driven environment., • Exposure to laboratory operations, compliance programs, and continuous improvement initiatives., • Collaborative culture focused on quality, safety, and professional growth., • Opportunity to make a direct impact on product quality and regulatory compliance. This is an excellent opportunity for a quality professional with GMP experience who enjoys documentation, compliance, and working closely with laboratory and manufacturing teams to maintain the highest quality standards. Job Type & Location This is a Contract to Hire position based out of Omaha, NE. Pay and Benefits The pay range for this position is $22.00 - $28.00/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors. 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 Omaha,NE. Application Deadline This position is anticipated to close on Oct 5, 2026. 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 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service. The company is an equal opportunity employer and will consider all applications withoutregard to race, sex, age, color, religion, national origin, veteran status, disability,sexual orientation, gender identity, genetic information or any characteristic protectedby law. If you would like to request a reasonable accommodation, such as the modification oradjustment of the job application process or interviewing process due to a disability,please email actalentaccommodation@actalentservices.com for other accommodation options. San Francisco Fair Chance Ordinance:Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in thecity and county of San Francisco, we will consider for employment qualified applicantswith arrest and conviction records. Massachusetts Lie Detector:It is unlawful in Massachusetts to require or administer a lie detector test as acondition of employment or continued employment. An employer who violates this lawshall be subject to criminal penalties and civil liability. Use of Artificial Intelligence (AI):We may use Artificial Intelligence (AI) to support parts of our hiring process,including sourcing, screening, and evaluating candidates. AI helps assess applicationsand qualifications, but final decisions are made by our hiring team. By applying, youacknowledge and agree that your application may be reviewed using AI tools.

Job DescriptionDescription: Job Title: Manufacturing Compliance Manager Reports To: Director of Manufacturing Department: Manufacturing Classification: Exempt, Full Time JOB SUMMARY: The Manufacturing Compliance Manager (MCM) will effectively manage compliance with quality and regulatory standards applicable to Pharmgate Omaha Manufacturing Operations. The Manager will develop and implement processes, procedures, and policies to meet all quality standards. This position assures efficient manufacturing by gathering and presenting data that reflects compliant production operations, authors deviation and investigation reports when there are atypical events. The MCM will be monitoring and analyzing data to identify trends and make recommendations for improvement. LEADERSHIP RESPONSIBILITIES: • Leads with influence across the manufacturing departments to support the Director in compliance with cGMPs as related to manufacturing operations., • Is informed and endorses the daily workflow and schedules of the department., • Conducts timely and constructive operational performance evaluations., • Provides routine Key Performance Indicator (KPI) snapshots and reports of compliance status., • Provides technical writing authoring and guidance within the department for deviations, investigations, IQ/OQ, and change controls as required. DUTIES/RESPONSIBILIITIES: • Assure manufacturing operates in accordance with FDA current Good Manufacturing Practice (GMP) requirements and guidelines., • Maintain Pharmgate Standard Operating Procedures (SOPs) by utilizing your professional background and accepted industry procedures and techniques in line with company policy requirements., • Interpret analytical findings to assess compliance or non-compliance with company and industry standards. Report documented findings to department director or production management and escalate atypical results as needed., • Completes company required forms in connection with project assignments., • Tracks non-compliance with granularity in regard to equipment, personnel operators, documents and training for compliance with SOPs and other records., • Provides non-compliance reports of operators and subordinates to area department leadership., • Develop a robust system for real-time batch record review with Manufacturing Quality and refers corrections back to subordinates for real-time and accurate edits/corrections., • Ensures compliance with federal, state, local, FDA, cGMPs organizational laws, regulations, guidelines, and best practices., • Provide immediate awareness to the Manufacturing Director regarding safety compliance to ensure a safe work environment., • Participate in team meetings as needed., • Contribute to department efforts in strategic planning, talent development, and training., • Responsible for timely investigation and deviation writing and editing, CAPA development and reporting results of analytical testing in compliance with quality management systems., • Performs technical writing and other duties as assigned. REQUIRED SKILLS/ABILITIES: • Thorough knowledge of cGMP manufacturing terminology, methods, and tools., • Working knowledge of Regulatory, cGMP and FDA regulations as required to ensure Pharmgate products and production units meet internal and external quality standards., • Ability to work collaboratively and communicate effectively., • Valid driver’s license., • Strong analytical skills, verbal and written communication abilities., • Utilizes organizational skills and time management and so effectively manages multiple priorities daily., • Proficient with Microsoft Office Suite, such as basic Excel® spreadsheet functions and MS-WORD®, word processing. PREFERRED SKILLS/ABILITIES: • Proficient with virtual meeting applications, SAP Business One, or other related software. EDUCATION AND EXPERIENCE: • Bachelor of Science degree in Chemistry, Microbiology or Biology or related field., • Minimum five (5) years’ experience in a cGMP manufacturing setting with an emphasis on quality focus experience; preferably in a pharmaceutical production facility. PHYSICAL REQUIREMENTS: • Prolonged periods of standing and walking through the facility., • Prolonged periods of sitting at a desk working on computers., • Must be able to occasionally lift 45 pounds from floor to waist level., • Visual acuity to inspect products and machinery., • Ability to occasionally climb stairs. This job description in no way states or implies that these are the only duties to be performed by this employee. He or she will be required to follow any other instructions and to perform any other duties requested by his or her supervisor. Requirements:

Job DescriptionABOUT US Rythm is the fastest-growing lab in America. We redefined at-home testing with the world’s easiest blood test and created a culture around monthly lab testing from home. We’ve processed millions of tests across all 50 states, and we do everything in-house, from sample testing and logistics to code, marketing, and design. That vertical integration gives us the speed, control, and creativity to shape the future of health and wellness. Our laboratory operates under CLIA certification and CAP accreditation, ensuring that all specimen handling and testing procedures meet rigorous regulatory and quality assurance standards. ABOUT THE ROLE Rythm Health is seeking a Laboratory Associate for its overnight shift to support day-to-day laboratory operations. The required work schedule is Monday through Friday, 11:00 PM–7:00 AM. The ideal candidate is reliable, detail-oriented, and comfortable working in a regulated clinical laboratory environment. This role involves data entry, sample accessioning, and processing in accordance with established procedures. WHAT YOU'LL DO • Accurately receive, accession, and track incoming specimens using laboratory information systems (LIS)., • Verify specimen integrity, labeling accuracy, and documentation compliance., • Aliquot and prepare blood samples according to established protocols., • Enter, review, and maintain accurate electronic laboratory records., • Adhere to CLIA/CAP-compliant SOPs, laboratory safety requirements, and quality assurance procedures., • Maintain a clean, organized, and compliant laboratory workspace., • Communicate specimen status and promptly escalate issues to the Lab Supervisor., • Support additional laboratory tasks as needed to meet operational demands., • *Work Schedule: Overnight shift required. Typical schedule will be Monday through Friday, 11:00 PM–7:00 AM, with flexibility based on operational needs. WHAT WE'RE LOOKING FOR • Bachelor’s degree or above in biology, chemistry, medical laboratory science, or a related field., • Comfortable working with computer software, LIS, and clinical lab equipment., • Strong attention to detail and organizational skills., • Ability to perform repetitive tasks accurately and efficiently., • Ability to handle blood specimens in a laboratory setting., • Reliable, punctual, and able to work both independently and as part of a team. WHAT’S IN IT FOR YOU? Rythm Health offers a benefits package which includes: • Highly competitive base salary., • Meaningful work that genuinely impacts people’s lives., • Equity: Stock Option allocation aligned with the scope and seniority of this role., • Monthly Rythm Health membership with full access to at-home blood testing and personalized health insights., • Generous paid time off policy., • 401(k)., • The opportunity to help define the future of personalized health., • High ownership and visibility from day one., • Small, collaborative, mission-driven team., • Ability to shape both product and customer experience culture early.

Job DescriptionDescription: Let’s Do great things—Together At Shive-Hattery, we believe great design starts with great people. We’re a full-service architecture and engineering firm with a legacy of collaboration, innovation, and putting people first, our clients and each other. If you’re looking for a place where your ideas matter and your growth is supported, you’ll feel at home here. Why This Role Matters As a NEPA Specialist with 5+ years of experience you’ll play a key role in supporting the firm and shaping projects that make a difference—from concept through completion. You’ll collaborate with talented teammates, contribute your expertise, and help us deliver thoughtful, high-quality solutions for those we serve. At Shive-Hattery, we help our clients navigate complex regulatory landscapes with ease. We ensure proactive compliance with key environmental laws, including the National Environmental Policy Act, Clean Water Act, Endangered Species Act, Migratory Bird Treaty Act, and Bald and Golden Eagle Protection Act. Our approach and use of the latest and best methods help clients achieve their project goals while protecting our natural resources. What You’ll Do • Lead natural resource evaluations and permitting efforts for numerous project types with the primary projects being transportation related, • Coordinating fieldwork and reporting, report writing, providing technical guidance to staff, and engaging proactively with clients, stakeholders, and contractors, • The ideal candidate will have established relationships with local, state, and federal permitting agencies, with focused experience in NEPA planning and compliance, and a strong understanding of key environmental programs, • Developing required transportation NEPA documentation for Categorical Exclusions and Environmental Assessments, interfacing with agencies (e.g., lead federal agency, state agencies, State Historic Preservation Office [SHPO], USACE, USFWS) to secure necessary reviews and guidance, and coordinating a multidisciplinary team, • Navigating federal, state, and local regulations, and liaising with transportation agencies such as DOT, and FHWA and keeping a pulse of evolving environmental law, • Engaging with engineers to integrate environmental considerations and facilitating cross disciplinary work Requirements: You don’t need to check every box to succeed here. If your experience aligns with many of the items below and you’re excited about the work we do, we encourage you to apply. • Comprehensive Background in Environmental regulatory compliance, transportation projects and coordination with DOT and FHWA is required., • Bachelor's degree in planning, biology, ecology, soils, environmental science, environmental policy, natural resource management, or related field, • Minimum of 5+ years of experience in environmental permitting and regulatory compliance, • Working knowledge of NEPA compliance in accordance with FHWA guidelines required, • Proficiency in interpreting site plans, topographic maps, aerial photographs, and other mapping resources, • Demonstrated capacity to work collaboratively with teams while independently pursuing NEPA compliance with a client-focused mindset What will make you stand out • Business acumen, a strong work ethic, and excellent problem solving-abilities, • Exceptional ability to communicate across written and spoken mediums, • Ability to contribute and work well with a team Our Commitment to You Great work happens when you feel secure in your future, confident in your support, and trusted to grow. That’s why our benefits support your health, financial stability, and life beyond work — including medical, dental and vision coverage, paid time off and holidays, 401(k) retirement savings, disability protection, wellness incentives, and flexibility. When we succeed, you share in that success. Guided by truth, trust, mentoring, and care, we’re committed to helping you build a lasting career. Who We Are Shive-Hattery is a privately held architecture and engineering consulting firm with design offices across the United States. Here, you’ll work alongside multidisciplinary teams delivering integrated design solutions for clients across industries. You’ll contribute to meaningful projects guided by our principle to design what matters and make our world a better place. You’re looking to build something great. So are we. Shive-Hattery is an Equal Opportunity Employer. We are committed to creating a diverse and inclusive workplace and do not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, veteran status, or any other legally protected status. This position is primarily performed in an office or hybrid environment and may require travel to project sites, other Shive-Hattery office locations or to meet with clients. A full clean driver’s license is required. The role involves sitting, standing, and working at a computer for extended periods. May also require lifting light to medium weight objects of up to 50 lbs., the wearing of PPE and navigating active construction sites. Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions of this role. U.S. Citizen, U.S. Person, or Immigration Status Requirements: We are unable to provide visa sponsorship now or in the future. Candidates must have current and ongoing authorization to work in the United States without employer sponsorship. If this role sounds like a fit for your skills and interests, we’d love to hear from you. Apply today and help us design what matters to make the world a better place. Interested applicants should submit their cover letter, resume, and portfolio for consideration. If you are unable to submit your portfolio due to size constraints, please include a link to your portfolio in your cover letter. Notice to Recruiters and Staffing Agencies: To protect the interests of all parties, Shive-Hattery and its partners will not accept unsolicited candidate submissions from a recruiter or staffing agency who is not operating under an executed recruiting or staffing services contract with Shive-Hattery. Please do not contact our employees directly in that regard or otherwise submit unsolicited candidate information in any form.

Job Description HIRING IMMEDIATELY!! Multiple Lab Technicians Needed!! Are you a Chemistry or Biology candidate looking for a FUN position working with GREAT people? If so, keep reading! Work for one of the largest laboratories in the Midwest. Gain or grow your science knowledge with valuable, real world laboratory experience! Competitive pay and AMAZING benefits if hired. Growing business with lots of opportunities for advancement! Compensation: Starting at $37,000 + 10% (average) in bonuses if hired!! (ask me about pay increases and benefits!) Shifts: First shift daytime hours, Monday-Friday (most laboratories) Benefits of being a Lab Technician: • Amazing benefits including 100% paid health insurance, profit sharing, PTO and vacation time, etc., • FUN position, exciting place to work with GREAT people and a solid management team!, • Well-established company, in business almost 50 years! What you'll do as a Lab Technician: • Perform various types of analysis on agricultural samples for clients!, • Work hands on with lab instruments and equipment, • Assist in daily laboratory practices and upkeep, • Work alongside the team to meet goals and process samples Requirements of a Lab Technician: • A Bachelor’s degree (required) in: Chemistry, Biochemistry, Biology, Microbiology, Animal Science, Agronomy, Agricultural Science, Horticulture, or Environmental Science, • Positive attitude and ability to work well with others, • Ability to stand 100% of the time Laboratories include: Soil Analysis, Plant Analysis, Chromatography, Microbiology, Wet Chemistry, Feed Analysis, Food Analysis, Pet Food Analysis Equal Opportunity Employer, including disability and protected veteran status Only best fit candidates will be contacted; must include resume to be considered Laboratory Technician, Laboratory Analyst, Laboratory Assistant, Laboratory, Lab, Biology, Chemistry, Science, Research Assistant

Job Description Company Description We are Olsson. We engineer and design solutions that improve the world around us. As a company, we promise to always be responsive, transparent, and focused on results – for our people, our clients, and our company. We're a people-centric firm, so it's no surprise our greatest asset is our people. The impact this creates is an environment that encourages our people to grow and be creative with their talents. This approach builds a culture that is uniquely Olsson. It allows us to grow our people as we grow our business. This, in turn, creates a lasting impact on the world around us. Job Description As a summer 2027 student intern with our Industrial Environmental team, you will perform meaningful, hands-on, real-world work that will transform your classroom experience and help you envision your future career. You will work closely with scientists, environmental professionals, and engineers on client projects related to mine reclamation, industrial water and wastewater treatment, environmental compliance, permitting, and solid waste management facilities. You will assist with environmental data collection, scientific research, technical analyses, and report preparation that support projects balancing client objectives and environmental stewardship. Depending on project needs, you may work in the office or the field helping with data collection, observations, and environmental assessments. Qualifications You are passionate about: • Working collaboratively with others., • Having ownership in the work you do., • Using your talents to positively affect communities.You bring to the team:, • Strong communication skills., • Ability to contribute and work well on a team., • Pursuing a bachelor's degree in environmental science, geology, environmental studies, biology or a related scientific field., • Interest in environmental field investigations, data collection, and scientific research., • Proficiency in Microsoft Word, Excel, and Outlook., • Ability to perform research and write technical reports., • Strong attention to detail., • Strong problem-solving and decision-making skills. #LI-DNP Additional Information Olsson specializes in engineering and design, client advisory services, planning, field services, and environmental. Improving the world has been our mindset from the very beginning, back when Olsson first opened for business in 1956. And it will be our mindset for years to come. As an Olsson employee, you will: • Receive a competitive 401(k) match, • Be empowered to build your career with tailored development paths, • Have the possibility for flexible work arrangements, • Engage in work that has a positive impact on communities, • Participate in a wellness program promoting balanced lifestyles In addition, full-time employees will receive our traditional benefits package (health care, vision, dental, paid time off, etc.) and the opportunity to participate in a bonus system that rewards performance. Olsson is an Equal Opportunity Employer. We encourage qualified minority, female, veteran, and disabled candidates to apply and be considered for open positions. We do not discriminate against any applicant for employment or any employee because of race, color, religion, national origin, sex, sexual orientation, gender identity, gender, disability, age, military status, or other protected status. Olsson understands the importance of privacy and is committed to protecting job applicants' personal information. Pursuant to the California Consumer Privacy Act, as amended by the California Privacy Rights Act (collectively, the "CCPA"), this notice explains Olsson's practices regarding the collection, use, and disclosure of personal information for job applicants residing in California. Please read this Notice carefully to understand our privacy practices. For more information about the types of information we collect and how we use it in connection with your general access and use of our website, please review our general California Privacy Notice here.

Job DescriptionABOUT US Rythm is the fastest-growing lab in America. We redefined at-home testing with the world’s easiest blood test and created a culture around monthly lab testing from home. We’ve processed millions of tests across all 50 states, and we do everything in-house, from sample testing and logistics to code, marketing, and design. That vertical integration gives us the speed, control, and creativity to shape the future of health and wellness. Our laboratory operates under CLIA certification and CAP accreditation, ensuring that all specimen handling and testing procedures meet rigorous regulatory and quality assurance standards. ABOUT THE ROLE Rythm Health is seeking a Laboratory Associate (2nd Shift) to support day-to-day laboratory operations. The required work schedule is Tuesday, Wednesday, Thursday, Saturday, and Sunday. The ideal candidate is reliable, detail-oriented, and comfortable working in a regulated clinical laboratory environment. This role involves data entry, sample accessioning, and processing in accordance with established procedures. WHAT YOU'LL DO • Accurately receive, accession, and track incoming specimens using laboratory information systems (LIS)., • Verify specimen integrity, labeling accuracy, and documentation compliance., • Aliquot and prepare blood samples according to established protocols., • Enter, review, and maintain accurate electronic laboratory records., • Adhere to CLIA/CAP-compliant SOPs, laboratory safety requirements, and quality assurance procedures., • Maintain a clean, organized, and compliant laboratory workspace., • Communicate specimen status and promptly escalate issues to the Lab Supervisor., • Support additional laboratory tasks as needed to meet operational demands., • *Work Schedule: 2nd shift required. Typical hours: 4:00 PM – 12:00 AM, with flexibility based on operational needs. WHAT WE'RE LOOKING FOR • Bachelor’s degree or above in biology, chemistry, medical laboratory science, or a related field., • Comfortable working with computer software, LIS, and clinical lab equipment., • Strong attention to detail and organizational skills., • Ability to perform repetitive tasks accurately and efficiently., • Ability to handle blood specimens in a laboratory setting., • Reliable, punctual, and able to work both independently and as part of a team. WHAT’S IN IT FOR YOU? Rythm Health offers a benefits package which includes: • Highly competitive base salary., • Flexible, remote-friendly work environment., • Meaningful work that genuinely impacts people’s lives., • Equity: Meaningful equity stake aligned with the scope and seniority of this role., • Monthly Rythm Health membership with full access to at-home blood testing and personalized health insights., • Unlimited vacation policy., • 401(k)., • The opportunity to help define the future of personalized health., • High ownership and visibility from day one., • Small, collaborative, mission-driven team., • Ability to shape both product and design culture early.

Job Description Simply Put, A Great Place to Work Benesch is a growing, multi-disciplined planning, engineering, and professional services firm. We enhance infrastructure and communities across the country – creating spaces and providing connections in ways that make a difference. We pride ourselves on being nimble enough to remain responsive to client needs yet large enough to offer exceptional bench strength. As a member of our team, you'll have an opportunity to draw from those resources when you need them and, likewise, contribute your expertise when you have something to share. At Benesch, we are looking for candidates with varied backgrounds and worldviews. We are committed to offering an inclusive work environment where everyone feels valued and respected. Statistics show that women and underrepresented groups are less likely to apply for a position if they don't meet 100% of the qualifications. If this statement resonates with you, don't be so hard on yourself—apply for the job! Environmental Scientist We are seeking to hire an entry-level Scientist to join our robust Natural Resources. This position will assist project managers with natural resource-based projects involving wetlands, threatened & endangered species, and water resource permitting issues. The ideal candidate will demonstrate the ability to be highly organized, multi-task, and navigate various complex projects. This role requires a proactive and detail-oriented individual with strong analytical skills, effective communication abilities, a proactive approach to problem-solving, and a commitment to taking initiative. Primary duties are located within an office or remote office environment with occasional fieldwork. Location The position will report out of our Omaha, NE, Lincoln, NE, Bellevue, NE, or Grand Island, NE office. The Impact You Will Have • Conduct fieldwork tasks such as wetland delineations, natural resources inventories, and environmental surveys., • Provide technical support for permit compliance and regulatory requirements., • Be prepared for frequent travel, including overnight stays both within and outside the state., • Assist project managers with various tasks to ensure project success., • Manage project schedules and budgets to ensure timely completion of deliverables., • Contribute to project proposals and collaborate with team members., • Stay updated on federal and regional regulations., • Build relationships with relevant agencies and represent Benesch as a subject matter expert., • Promote a culture of safety awareness and professionalism in the workplace.What We Are Looking For, • Bachelor's degree in Biology or Environmental Sciences with 1-4 years of relevant work experience., • Prior experience in wetland delineation, botanical surveys, and surveys related to threatened and endangered species., • Familiarity with native vegetation identification and state and federal environmental permitting., • Previous experience in renewable energy projects is a plus., • Knowledge of state and federal permitting processes is desired., • Proficiency in technical writing and experience in quality assurance/quality control of data and reporting are essential.Why Benesch It's simple. We invest in our people, not just our projects. • Career growth that's real with leadership development, training, and clear paths forward, • Strong financial future with up to 9% retirement contribution for benefit-eligible employees, • Flexibility that works with schedules that support your life, • Time to recharge with generous paid time off and parental leave for benefit-eligible employees, • Support beyond work through mentorship, hands-on experience, and opportunities to make an impact from day one Whether you're starting your career or bringing years of experience, you'll have the support and exposure to grow here. Explore our full benefits here: Click here Equal Opportunity & Accessibility At Benesch, we believe great work starts with great people and that means creating a workplace where everyone has the opportunity to succeed. Benesch is firmly committed to Equal Employment Opportunity (EEO) and prohibits employment discrimination for employees and applicants in all protected groups, including veterans and individuals with disabilities, or other status protected by federal, state, and local laws. Benesch is committed to working with and providing reasonable accommodation to applicants with a physical disability or other impairment. If you are limited in your ability or are unable to access Benesch's Careers website due to a physical disability or other impairment, you may request a reasonable accommodation by emailing TalentAcquisition@benesch.com. This option is only available to those in need of an accommodation due to a disability or other impairment. Please do not use this as an alternative method for general inquiries or status on applications, as you will not receive a response. Reasonable requests will be responded to as soon as possible on a case-by-case basis. If you are based in California, we encourage you to read this important information for California residents linked here. Know your Rights: Workplace Discrimination is Illegal We will be accepting applications on an ongoing basis until a candidate is found. External Recruiters and Staffing Agencies Benesch shall have no obligation to compensate any external recruiter or search firm for candidate submissions made without a valid, current, and fully executed agreement. Submission of candidate information does not establish entitlement to a fee. All recruiting activity must be coordinated and authorized through the Benesch Talent Acquisition team. Please direct all communications to TalentAcquisition@Benesch.com

Job Description Certified Group is committed to partnering with customers to deliver innovative scientific solutions and expertise – So The World Can Trust In What It Consumes™. Our network of 30+ North American and European laboratories serves the food & beverage, dietary supplements, cosmetics, OTC, tobacco/nicotine, cannabis, and hemp industries. Our Brands Certified Group is comprised of a set of specialized brands that collectively deliver laboratory testing, regulatory consulting, and certification & audit services across highly regulated industries: • Certified Laboratories – Provides comprehensive analytical and microbiological testing, primarily supporting food, beverage, cosmetics, OTC, and dietary supplement industries., • Food Safety Net Services (FSNS) – A leading network of ISO-accredited laboratories across North America, focused on food safety testing, operational support, and technical services for the food industry., • Labstat – A global leader in contract research and testing for nicotine, tobacco, cannabis, hemp, and next-generation products, with deep expertise in analytical chemistry and toxicology., • EAS Consulting Group – A regulatory consulting firm offering expert guidance, training, and auditing support across FDA, USDA, and other regulated sectors, powered by a large network of independent advisors., • FSNS Certification & Audit – Provides accredited third-party auditing and certification services, including food safety, animal welfare, and GMP programs. Position Summary The Logistics Supervisor is responsible for overseeing daily logistics operations within a laboratory environment, including managing a fleet of couriers, coordinating specimen/sample transportation, and maintaining accurate inventory levels. This role ensures timely, compliant, and efficient movement of materials while supporting overall lab operations. Responsibilities: Courier & Fleet Management • Supervise and coordinate daily activities of courier staff, including scheduling, routing, and performance monitoring, • Ensure timely pickup and delivery of laboratory specimens, supplies, and documents, • Monitor fleet usage, maintenance schedules, and vehicle compliance (licenses, inspections, etc.), • Optimize delivery routes to improve efficiency and reduce costs Inventory Management • Oversee inventory of laboratory supplies, reagents, and consumables, • Maintain accurate inventory records using tracking systems, • Conduct regular audits and cycle counts, • Coordinate ordering and replenishment to prevent shortages or overstock Logistics Coordination • Ensure proper handling, packaging, and transport of lab materials in compliance with regulatory and safety standards, • Collaborate with lab staff to prioritize urgent or time-sensitive deliveries, • Troubleshoot delays, delivery issues, or operational disruptions Compliance & Safety • Enforce adherence to OSHA, DOT, and laboratory safety regulations, • Train staff on proper handling of biological or hazardous materials, • Maintain documentation for audits and inspections Team Leadership • Train, mentor, and evaluate courier and logistics personnel, • Develop schedules and manage staffing levels, • Promote a culture of accountability, safety, and continuous improvement Reporting & Process Improvement • Track and report key performance metrics (delivery times, error rates, inventory accuracy), • Identify process inefficiencies and implement improvements, • Support implementation of logistics or inventory management systems Qualifications: Education & Experience • Associate's or Bachelor's degree in Logistics, Supply Chain, Biology, or related field (preferred), • 3–5+ years of logistics, transportation, or inventory management experience, • Prior experience in a laboratory, healthcare, or regulated environment strongly preferred, • Previous supervisory experience required Skills & Competencies • Strong organizational and multitasking skills, • Knowledge of inventory systems and logistics software, • Understanding of laboratory handling procedures and compliance standards, • Excellent leadership and communication skills, • Problem-solving and decision-making ability under pressure Working Conditions & Schedule • Laboratory and warehouse environment, • Schedule is typically a hybrid between 1st and 2nd shift based on business needs, • Must be flexible and willing to work off-hours, including early mornings, evenings, weekends, or on-call support as needed, • May require occasional lifting (up to 50 lbs) By applying, you acknowledge that Certified Group will process your personal information for recruitment and hiring purposes in accordance with our Applicant Privacy Policy. California residents may review additional information about how we collect and use personal information, including retention and rights, in our California Notice at Collection. To view our Privacy Policy, click the link here: Certified Group Privacy Policy We are an Equal Opportunity Employer and make employment decisions without regard to protected characteristics under applicable law.

Job Description HIRING IMMEDIATELY!! MULTIPLE POSITIONS Entry-Level Lab Technicians needed! Are you looking to get your foot in the door with a great company with awesome people? If so, keep reading! Compensation: $18 per hour (overtime paid at $27 per hour!!) Shifts: First shift DAYTIME hours, Monday-Friday Benefits of being a Entry-Level Lab Technician: • FUN position, exciting place to work with GREAT people and a solid management team!, • Well-established company, in business almost 50 years!, • Amazing benefits including 100% paid health insurance, profit sharing, PTO and vacation time, etc. What you'll do as a Entry-Level Lab Technician: • Perform analysis on samples for clients!, • Work hands on with lab instruments and equipment, • Assist in daily laboratory practices and upkeep, • Work alongside the team to meet goals and process samples Requirements of a Entry-Level Lab Technician: • High School Diploma (required), • Previous laboratory experience highly preferred, • Positive attitude and ability to work well with others, • Ability to stand 100% of the time Equal Opportunity Employer, including disability and protected veteran status Only best fit candidates will be contacted Laboratory Technician, Laboratory Analyst, Laboratory Assistant, Laboratory, Lab, Biology, Chemistry, Science, Research Assistant

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