Chemist Jobs in Utah

The Receiving Chemist is responsible for Lab Pack Processing and Drum Receiving/Coding. We offer a free shuttle service for employees commuting from the surrounding area (SLC, West Valley City, Tooele, and Grantsville) to our Aragonite facility located off of Exit-56 on I-80. We are searching for a reliable and team-oriented individual with an excellent commitment to safety to join our growing team! Why work for Clean Harbors? Health and Safety is our #1 priority and we live it 3-6-5! Competitive pay and benefits Comprehensive health benefits coverage after 30 days Group 401K with company matching component Generous paid time off, company paid training and tuition reimbursement Positive and safe work environments Responsibilities Ensuring that Health and Safety is the number one priority by complying with all safe work practices, policies, and processes and acting in a safe manner at all times Offloads containers from Van trailers upon arrival at the facility Receives all incoming containers and properly codes all waste for disposal processing Completes all paperwork associated with consolidation process and performs waste tracking operations through Clean Harbors proprietary software, WIN Samples all incoming drums and performs basic chemical analysis of samples following prescribed procedures Calibrates and utilizes lab instrumentation required to run basic analysis, completes all paperwork associated with analysis and drum sampling, ensures that all work meets applicable QA/QC guidelines Assures all drums are assigned proper disposal process code and/or outbound profile, responsible for knowledge of Clean Harbors proprietary WIN system applicable to receiving, routing, and billing of drums Conveys critical verbal and written information to internal and external stakeholders Ensures real time tracking of all containers via Clean Harbors WIN system in conjunction with handheld scanners Supply management in their area of responsibility, and best management practices including proper housekeeping Other duties as assigned Qualifications High School diploma or equivalent required 1+ Year(s) experience with Windows-based computer applications 1+ year Warehouse or Plant experience preferred Excellent written and verbal communication skills Previous experience in one or more of the following fields preferred: Warehouse, Quality Control, Chemical Handling, Laboratory, or Inventory Management Excellent attention to detail and organizational skills Forklift experience is a plus Must be clean shaven Ability to work in adverse environment such as cold and heat Join our team today! To learn more about our company, and to apply online for this exciting opportunity, visit us at ********************************* Clean Harbors is the leading provider of environmental, energy and industrial services throughout North America. The Company serves a diverse customer base, including a majority of the Fortune 500 companies, thousands of smaller private entities and numerous federal, state, provincial and local governmental agencies. Through its Safety-Kleen subsidiary, Clean Harbors also is a premier provider of used oil recycling and re-refining, parts washers and environmental services for the small quantity generator market. Headquartered in Norwell, Massachusetts, Clean Harbors has waste disposal facilities and service locations throughout the United States and Canada, as well as Mexico and Puerto Rico. We are an equal opportunity in employer to all individuals regardless of race, color, religion, sex, age, national origin, pregnancy, familial status, disability status, veteran status, citizenship status, genetic information or any other characteristic protected under Federal, State or Local law. Clean Harbors is a Military & Veteran friendly company. *CH #LI-AN1

Avarint is a wholly owned subsidiary of CUBRC Inc. Pending Contract Award*** Avarint's Chemical Sciences Group is seeking a Chemist to support an experimental team conducting Research, Development, Test and Evaluation (RDT&E) at Dugway Proving Ground, UT. Primary duties will include: Planning and executing RDT&E projects with minimal guidance to include designing experiments, collecting and analyzing data, and troubleshooting technical problems. Working with highly toxic chemicals and materials and providing technical expertise and support to the development of Standard Operating Procedures (SOPs). Operating, maintaining, and troubleshooting of analytical test equipment (GC, GC-MS, and/or LC-MS/MS) and working closely with project managers to adjust methods to meet project objectives. Reviewing and continuously improving the QA/QC program to ensure that all reported data is accurate, complete, reliable, and of high confidence. Developing analysis reports that include methods, procedures, and analytical data including interpretation of results and annotating the file documentation; and performing technical and/or administrative reviews of files, reports, data sets, results, and conclusions. Maintaining a safe laboratory work environment in accordance with all documented laboratory procedures. The position also requires that the selected candidate possess: Strong hands-on laboratory skills with respect to GC-MS and/or LC-MS/MS instrument operation and sample analysis. Excellent organizational skills and communication skills (oral and written) and the ability to appropriately communicate with colleagues, management and clients to plan and execute duties. Deep attention to detail and the flexibility and ability to work both independently and as part of a team. Requirements THE FOLLOWING REQUIREMENTS MUST BE MET TO BE CONSIDERED FOR THIS POSITION: Minimum Qualifications B.S. in Chemistry, Analytical Chemistry, Biochemistry or other related physical science or engineering discipline; or an equivalent combination of education and experience. Experience with Microsoft Office software including MS Word, Outlook, Excel and PowerPoint. Experience with gas chromatography, GC-MS and/or LC-MS/MS. Ability to obtain and maintain a DoD Secret security clearance. U.S. citizenship. A medical examination will be required to ensure ability to perform duties and wear personal protective equipment. THE FOLLOWING REQUIREMENTS ARE DESIRED BUT NOT REQUIRED FOR THIS POSITION: An active DoD security clearance (S or TS). Experience working with Miniature Chemical Agent Monitoring Systems (MINICAMS) for workplace air monitoring during test operations. Experience with Microsoft Office software (Access, Project, Outlook, SharePoint and Teams). Experience in contract research, working for the federal government and/or private organizations. Why Avarint: 401K - No waiting period. 100% vested on the date of hire. 3% company contribution in the first year of employment, company contribution increases over time. The employee is not required to contribute to the plan to receive Avarint contribution. Health Insurance - No waiting period - competitive costs. Dental and vision insurance after 6 months - Employer-paid benefit for employees and dependents. Life Insurance after 6 months - Employer paid benefit for the employee. Generous paid time off, unlimited sick time, and 9 paid holidays. The candidate will be subject to a government security investigation and must meet eligibility requirements for access to classified information. U.S. citizenship is required. The position requires participation in a Chemical Personnel Reliability Program (CPRP), administered by the U.S. Army. A medical examination will be required to ensure the ability to perform duties and wear personal protective equipment. The candidate will also be required to comply with a Drug Testing Program. Avarint is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status.

Performs cyclotron operation, manufacturing, and quality control for routine and research radiopharmaceuticals for positron emission tomography ( PET ). Incumbent must comply with radiation safety procedures, cGMP, and FDA requirements. Operates, and assists in maintenance and validation of manufacturing and analytical equipment. Follows all standard operating procedures and performs additional duties as directed by management. Must be motivated, team oriented and committed to expanding their knowledge and experience in a clinically oriented academic program. Incumbent will experience moderate exposure to hazardous materials or physical risk, which requires adhering to radiation safety practices. Full time position involving a variable schedule around production demands. The typical work week will be Monday through Friday 11:30 pm - 7:30 am. These time frames may need to be adjusted as production demands change. In very rare instances a weekend shift may be required. Huntsman Cancer Institute is committed to cancer prevention, care, and survivorship for all communities within the area we serve - which includes Idaho, Montana, Nevada, Utah, and Wyoming - with impact worldwide. Partnerships with individuals, communities, and many other entities are crucial to our work. Huntsman Cancer Institute values cancer-related health equity, and inclusion as integral to our guiding principle to serve our patients and their communities, and our commitment to foster a culture of belonging for all within our organization. In your cover letter or during your interview process, we invite you to share how your personal and professional experiences have prepared you to serve as a member of our team as we work to reduce the cancer burden experienced by all people and communities. This may include description of your prior experiences related to research, prevention, clinical care, community engagement/outreach, training, administration, or other areas relevant to Huntsman Cancer Institute's mission and this position. Learn more here Responsibilities As a Radiochemist your duties will be highly varied from time to time and may include but not be limited to: Under the direction of the management, assists with all activities involved in developing and preparing radiopharmaceuticals for clinical and research use. Operates, assists in maintenance and troubleshoots the cyclotron and associated equipment in compliance with protocols and good ALARA radiation safety practices. Operates automated radiochemistry synthesis equipment in compliance with protocols and current Good Manufacturing Practices (cGMP) and FDA regulations. Performs quality control of radiopharmaceuticals according to standard operating procedures. Troubleshoots cyclotron laboratory equipment using mechanical, electrical and basic science skills. Develops and performs new processes or protocols for validation, manufacturing and quality control. Assists management in developing, improving and maintaining protocols, applications, and licenses as required for routine radiopharmaceutical production. Assists in packaging and shipping of radioactive material in compliance with all state and federal regulations. Assists with the return and cleaning of shipping containers as assigned. Assists in preparing regulatory documents for submission to the FDA . Complete and maintain periodic training for GMP , equipment, radiation safety, SOPs, HIPAA , and others as required. Minimum Qualifications · Bachelor of Science Radiochemistry, Chemistry, or Biochemistry. Other science related degrees will also be considered with equivalent experience. · 2+ years of work in a research, analytical or pharmaceutical laboratory. Other types of experience similar to these areas will also be considered. · 2+ years of experience in working with analytical equipment such as HPLC , GC, and IC. · Detail oriented, self-directed, able to work autonomously and able to multitask effectively. · Ability to read, listen and understand technical direction, policies and procedures. · Applicants must demonstrate the potential ability to perform the essential functions of the job as outlined in the position description and general responsibilities. · Physical demands: Clear speech, good hearing and at least 20/20 corrected vision (which can include the use of glasses, contact lenses, etc.). Ability to lift up to 110 lbs. · Must satisfactorily pass a background test and not be debarred from any activities related to manufacturing radiopharmaceuticals.

Lab Assistant opening near Spanish Valley, Utah. This is a permanent, full-time position with great pay and benefits. Click APPLY today. If you are interested in learning more, or if you are a healthcare professional looking for a new position contact Marina Setaro - call/text 617-430-7080 or email your resume to marina@ka-recruiting.com Or book a 5 minute phone call here: https://calendly.com/marinaka/job-opportunity-information-meeting

Duration: 6+ month Job Description: Under general supervision, performs cGMP laboratory analyses of Finished products and in process materials. Performs stability testing for Finished products. Performs maintenance and calibration of analytical instruments. Minimum Qualifications: Bachelor's Degree in Science or related science field from an accredited college or university and one (1) year related laboratory experience or an equivalent combination of education and experience. Experience and Skills: •Usage of GC and HPLC chromatographic equipment, as well as UV/VIS, and FTIR operation methods and techniques. •Business, scientific and personal computer hardware and software applications. •Business English usage, spelling, grammar and punctuation. •Wet Chemistry and Chemistry related to sampling methods, quality control systems, analysis and documentation practices and procedures. •Knowledge of or ability to learn FDA, cGLP, cGMP, USP, EP and SOP or other applicable regulatory and safety compliance guidelines. •Performing testing accurately and precisely. •Responding to routine inquiries from management, employees and regulatory agencies. •Communicating clearly and concisely, both orally and in writing. •Managing multiple projects, duties and assignments. •Establishing and maintaining cooperative working relationships with others. Essential functions include: *Carries out responsibilities in accordance with the organization's policies, procedures and state, federal and local laws. *Operates general analytical instruments during the testing of finished products using HPLC, UPLC, GC-FID, UV-VIS, FTIR, automatic titrators, Dissolution Apparatus *Performs physical testing such as viscosity testing, Instron testing, and microscopy . *Performs wet chemistry tests on samples such as pH, titration, gravimetry and prepares standard, sample, and buffer solutions as required by test methods and performs all necessary calculations associated. *Labels, transcribes and records documentation such as report sheets and laboratory notebooks as required by SOPs. *Cleans, maintains and calibrates laboratory equipment to ensure compliance with current Good Manufacturing Procedures (cGMP). *Meets project deadlines and performance standards as assigned. *Complies with all Company policies and procedures, including safety rules and regulations *Performs investigations and troubleshooting of analytical test methods and lab instruments. *Performs investigation and writes reports on findings, conclusion and identify corrective actions/preventative actions. *Carries out quantitative and qualitative analyses in support of method comparisons, method transfers, method validations, product in-use study. *Train junior level scientist and technician and participate in identifying process to improve efficiency in laboratory testing. *Assist in organizing, staging and pulling samples for stability studies. *Assist in creating database for stability sample pull, staging sample and test schedules. *Performs related duties as assigned. Qualifications Minimum Qualifications: Bachelor's Degree in Science or related science field from an accredited college or university and one (1) year related laboratory experience or an equivalent combination of education and experience. Experience and Skills: •Usage of GC and HPLC chromatographic equipment, as well as UV/VIS, and FTIR operation methods and techniques. •Business, scientific and personal computer hardware and software applications. •Business English usage, spelling, grammar and punctuation. •Wet Chemistry and Chemistry related to sampling methods, quality control systems, analysis and documentation practices and procedures. •Knowledge of or ability to learn FDA, cGLP, cGMP, USP, EP and SOP or other applicable regulatory and safety compliance guidelines. •Performing testing accurately and precisely. •Responding to routine inquiries from management, employees and regulatory agencies. •Communicating clearly and concisely, both orally and in writing. •Managing multiple projects, duties and assignments. •Establishing and maintaining cooperative working relationships with others. Additional Information All your information will be kept confidential according to EEO guidelines.

What you'll do: * Use analytical techniques & instrumentation to characterize energetic material properties & demonstrate robustness of those materials. * Plan & execute experiments, analyze test results & data, document results in lab notebook, determine next steps in energetic material development. * Manage, implement, and upgrade test & build procedures * Contribute to energetic material qualification and validation through use of Autoliv Product Development Systems. * Interface with internal and external customers by providing and delivering professional technical presentations. What is required: * Master with experience (+5 years) or PHD recently graduated in Organic Chemistry. * Preferred with experience in developing energetic materials including testing, research, development, and industrialization. * Hands on and practical exposure to energetic materials including fuels, oxidizers, ballistic additives, and other manufacturing aides. * An understanding of analytical techniques used to characterize energetic materials is highly desirable. These techniques include DSC, TGA, TMA, XRD, FTIR, moisture adsorption, various types of calorimetry, Ion chromatography, gas chromatography, surface area, particle size distribution, porosity, ICP, and wet analytical techniques. * A working knowledge of standard safety practices used when handling energetic materials and the willingness to use these practices on a daily basis is essential. * Statistical Design of Experiments background desirable. * Proficiency with Excel, Word, Power Point, SharePoint. What's in it for you: * Attractive compensation package * Flexible Options (schedule, etc) * Recognition awards, company events, family events, university discount options and many more perks. * Gender Pay Equality Autoliv is proud to be an equal opportunity employer. Autoliv does not discriminate in any aspect of employment based on race, color, religion, national origin, ancestry, gender, sexual orientation, gender identify and/or expression, age, disability, or any other characteristic protected by federal, state, or local employment discrimination laws where Autoliv does business.

Selene Holdings is a multiple-lines business financial services firm with a mortgage servicing company, a loan diligence company, a title company, an insurance brokerage, and a real estate owned company. We have office locations in Dallas, TX, Jacksonville, FL, and Salt Lake City, UT. Founded in 2007 to address needs in the mortgage industry, Selene strives to provide amazing client and borrower experiences. A positive attitude coupled with proven creative thinking and actions are all attributes we seek in every one of our employees. If you want to make a difference, then Selene is the place for you! Position Summary: Quality Control Analyst focused on controlling a high quality product, enhancing loan review processes and developing specialist expertise for long term career growth. Essential Duties and Responsibilities include the following. Other duties may be assigned. Responsible for the Quality Control examination of loan reviews completed by Loan Review Analysts. Provide real time loan kick back feedback to Loan Review Analysts pertaining to errors and determining corrective actions. Ensure regulatory compliance for loans reviewed. Escalate error trends to management. Develop deep understanding of specific client guidelines. Handle escalated and countered client conditions with minimal guidance. Assists with loan review system testing and enhancement. Ongoing development of subject matter expertise - aim to become go to subject matter expert for various specialist loan review QC topics. Assist with problem solving, issue resolution and loan review guidance. Assist in providing guidance on daily matters, such as, questions regarding Underwriting Guidelines or Compliance questions relating to TRID, Reg X, TILA or others to LRAs. Maintains high level of confidentiality to protect privacy rights. Adheres to internal controls to reduce errors and customer complaints. Responsive to internal and external customers' needs in a timely, accurate and professional manner. Qualifications: To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. The qualified candidate must have: Maintains a current knowledge of underwriting guidelines, investor guidelines, regulatory compliance and TRID practices. Minimum 3-5 years mortgage underwriting and mortgage quality control within the origination or due diligence space. Strong understanding of condition clearing processes and their impact on loan grades. Basic understanding of the credit rating agency requirements. Knowledge of USPAP standards, supplemental valuation products and reconciliation. Ability to produce underwriting reports, analyze results, identify issues and take corrective actions. Experienced with reading, analyzing and understanding various loan servicer pay histories and servicing documentation. Developing leadership skills with the ability and experience to manage people. Effectiveness as a team player. Ability to easily prioritize job duties according to the needs of the company. Strong sense of professionalism and positivity. Excellent oral and written communication skills. Ability to develop rapport with all levels of associates and establish credibility. Excellent listening skills and the ability to use good judgment. Strong interpersonal/relationship building skills. Problem solving and decision making ability. Ability to produce quality work. Ability to think and solve problems strategically. Strong analytical and organizational skills. Excellent attention to detail. Ability to multi-task and consistently meet multiple deadlines. Competencies: To perform the job successfully, an individual should demonstrate the following: Business Acumen - Understands business implications of decisions. Conducts cost-benefit analysis. Displays orientation of profitability. Demonstrates knowledge of market and competition. Aligns work with strategic goals. Business Ethics - Treats people with respect. Keep commitments. Inspires the trust of others. Works with integrity and ethically. Upholds organizational values. Change Management - Develops workable implementation plans. Communicates change effectively. Builds commitment and overcomes resistance. Prepares and supports those affected by change. Monitors transition and evaluates results. Leadership - Exhibits confidence in self and others. Inspires respect and trust. Reacts well under pressure. Shows courage to take action. Managing People - Includes staff in planning, decision-making, facilitating and process improvement. Takes responsibility for subordinates' activities. Makes self-available to staff. Provides regular performance feedback. Develops subordinates' skills and encourages growth. Solicits and applies customer feedback (internal and external). Fosters quality focus in others; Improves processes, products and services. Continually works to improve supervisory skills. Planning & Organizing - Prioritizes and plans work activities. Uses time efficiently. Plans for additional resources. Sets goals and objectives. Organizes or schedules other people and their tasks. Develops realistic action plans. Education/Experience: Minimum 3-5 years' experience with emphasis on non-agency underwriting and QC desired. Experience in second level reviews; escalations and performance management required. Bachelor's degree preferred. Computer Skills: Working knowledge of and experience with Microsoft Office (Word, Excel, and Outlook). Previous experience with mortgage due diligence software, Andor, MSP, Black Knight/LPS and Fiserv preferred. Certificates and Licenses: N/A Travel: N/A Work Environment: The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. This position works in a typical office environment with moderate noise levels. Physical Demands: The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. The employee is regularly required to sit while working at a desk, occasionally standing, walking, and using hands to lift and/or move up to 25 pounds. Needs to be able to talk and hear, but no special vision is required beyond the ability to see in order to read. The above is not intended to be an all-inclusive list of duties and standards of the position. Incumbents will follow any other instructions, and perform any other related duties, as assigned by their supervisor. Why Selene? Benefits Selene Finance LP is committed to the total wellbeing of its employees and therefore offers one of the best benefits packages available in the industry today, which includes: Paid Time Off (PTO) Medical, Dental &Vision Employee Assistance Program Flexible Spending Account Health Savings Account Paid Holidays Company paid Life Insurance Matching 401(k) Plan The job requirements listed above are representative of the knowledge, skills, and/or abilities required. This job description is not an inclusive list of all duties and responsibilities of this position. Incumbents will be required to follow any other job-related instructions and to perform any other job-related duties requested by any person authorized to give instructions or assignments. Selene reserves the right to amend and change responsibilities to meet business and organizational needs. Privacy Policy - Selene (seleneadvantage.com)

Neurodegenerative diseases are one of the largest medical challenges of our time. Denali Therapeutics is a biotechnology company dedicated to developing breakthrough therapies for neurodegenerative diseases through our deep commitment to degeneration biology and principles of translational medicine. Denali is founded on the collaboration of leading scientists, industry experts, and investors who share the vision that scientific discovery energetically applied to translational medicine is the key to delivering effective therapies to patients. We invite you to consider an opportunity with Denali to help achieve our goal of delivering meaningful therapeutics to patients. This role will play a key role in executing and reports analytical/chemistry test methods for raw materials, drug substance and drug product for large molecule clinical and commercial products. Key Accountabilities/ Core Job Responsibilities: * Performs implementation and execution of routine and ad hoc chemical and analytical testing for raw materials and large molecule drug substance and drug product. * Supports the qualification and implementation of USP/EP methods and product specific methods as part of new product introduction and technology transfer. * Supports stability testing of drug substance and drug product for all timepoints and conditions. * Supports quality events such as CAPA, Change Control, Deviations, and LIR/OOS as subject matter expert for QC Chemistry * Generates, analyzes, and reports data and takes appropriate action * Works within LabWare LIMS for execution of methods, data trending and report issuance. * Reviews documentation for product disposition, generates COA/COC and batch summary reports * Works with accuracy, urgency and a continuous improvement perspective * Provides flexible support for on-call or outside normal business hours if required Qualifications/Skills: * BS in Chemistry or equivalent science * 4+ years of experience working in GMP regulated chemistry laboratory * Large molecule experience preferred * Familiarity with GMP regulations * Knowledge of current USP/Ph. Eur./FDA/ISO/GMP standards and guidance * Ability to work with independently * Build productive relationships with internal teams and external sources * Well-developed verbal and written communication skills * Excellence in execution through accuracy, right first time and a proactive nature * Physical requirements- must be able to put on specialized gowning, lift and manipulate items over 25 lbs, climb ladders, stand for multiple hours at a time * Strong collaboration and project management skills * Familiar with Master Control and LabWare LIMS Compensation for the role will depend on a number of factors, including a candidate's qualifications, skills, competencies, and experience. Denali offers a competitive total rewards package, which includes a 401k, healthcare coverage, ESPP and a broad range of other benefits. Learn more at ****************************************** This compensation and benefits information is based on Denali's good faith estimate as of the date of publication and may be modified in the future.This compensation and benefits information is based on Denali's good faith estimate as of the date of publication and may be modified in the future. Denali is committed to its core company value of unity by creating a diverse and inclusive environment. We are proud to be an equal opportunity employer and do not discriminate against any employee or applicant for employment because of race, color, sex, age, national origin, religion, sexual orientation, gender identity and/or expression, status as a veteran, basis of disability, or any other federal, state, or local protected class.

Certified Group is committed to delivering expert solutions and quality testing our customers can feel confident in - on time, every time - so the world can trust in what it consumes. As a leading North American provider of laboratory testing, regulatory consulting, and certification & audit services, Certified Group includes Food Safety Net Services (FSNS), FSNS Certification & Audit, Certified Laboratories, EAS Consulting Group, and Labstat International Inc. Certified Group provides analytical testing and regulatory guidance services in the food & beverage, dietary supplements & NHP, cosmetics, OTC, personal care, tobacco, nicotine, cannabis, and hemp industries. We have embarked on an important journey to unify and strengthen our culture by living these core values: Start with the Customer, Drive to Deliver, Commit to Safety and Quality, and Believe in the Team - including believing in you. We are currently looking for a Pathogen Lab Analyst to join our growing team! Job Summary: Perform analytical and microbiological testing of food products, ingredients, and environmentals. The position performs the application and evaluation of approved microbiological techniques and methodologies. Essential Responsibilities: * Accurately perform and read test results and notify Laboratory Management of deviations * Prepare and analyze samples for indicator organisms, pathogens, and chemistries * Apply aseptic/microbiological techniques in daily workload * Report inventory and expendable supplies/materials needed for testing requirements * Provide routine preventive maintenance by daily cleaning, sanitizing, trash disposal, and equipment quality control * Assist in quality duties to by taking incubator temperatures, inoculating control organisms, running media controls, etc. * Pursue an assigned series of processes, procedures, or techniques in accordance with FSNS policies/procedures and customer requirements * Maintain a high degree of technical competence by reading scientific journals, attending professional workshops, and being aware of food industry issues and trends * Perform all activities in a neat, safe, hygienic, and efficient manner * Share information in an open and timely manner * Assisting with managing priorities and schedule such that individual goals as well as team goals are achieved with encouraged participation in the Food Safety Net Services Team * Responsible for the safety of oneself and others working within their area Education & Experience: * Associate degree in Life Science or related field with two or more years of laboratory experience, preferred * Two or more years of experience in a commercial food-testing or analytical laboratory * Or equivalent combination of education and experience * Working knowledge of aseptic sampling technique, automated lab equipment, and acceptable methods and procedures * Familiarity with GLP, OSHA guidelines, FDA, BAM, APHA, ISO, and USP methods and procedures * Broad knowledge of concepts, practices, and procedures of a food testing laboratory * Ability to travel when necessary Physical Demands/Work Environment: * Dexterity of hands and fingers to operate a computer keyboard, mouse and to handle other communications/computer components * Potential exposure to odors, fumes, airborne particles, hazardous chemicals, and microbiological pathogens * Noise level varies from quiet to loud * Temperature varies from hot to cold * Interactive and fast-paced team oriented tasks * Overnight Travel is required at the discretion of management * Occasionally lift and/or move up to 25 pounds * Color vision and depth perception Benefits: * Progressive 401k Retirement Savings Plan * Employer Paid Short- Term and Long-Term Disability, and Life Insurance * Group Medical * Tuition Reimbursement * Flexible Spending Accounts * Dental * Paid Holidays and Time Off Certified Group values diversity in its workforce. The company is firmly committed to a policy of Equal Opportunity and will administer its policies in a manner that treats each employee and applicant for employment on the basis of merit. Certified Group will take affirmative action to seek out qualified applicants without regard to race, color, religion, sex, national origin, age, handicap, or veteran status.

Salt Lake City Regular MERIEUX NUTRISCIENCES As a trusted partner, our Public Health mission is to make food systems safer, healthier and more sustainable. Throughout our global network in 27 countries, we offer to our customers a wide range of testing and innovative solutions dedicated to preventing health risks related to food, environment and consumer goods. External growth has been a key pillar of our history with more than 40 acquisitions completed in the last 10 years. If you want to contribute to an inspiring long-term purpose, to be part of a fast growing company on a high-value market with significant build-up opportunities, and to grow in an entrepreneurial and warm environment, join us! YOUR DAY TO DAY LIFE We are looking for a Chemistry Technician in 1945 Fremont Drive, Salt Lake City, UT 84104 USA. Your mission will be to: * Composting and grinding of samples for analysis as required. * Perform chemical analyses such as protein, moisture, fat, ash, and other components. * Prepare sample for analysis according to procedure. Retrieve samples from designated areas (e.g. log-in, sample storage). * Perform chemical analyses of macronutrients, micronutrients or other parameters as designated. * Extract desired component from sample with appropriate processes so that concentration can be determined. * Prepare standards and reagents that are needed for the analysis procedure. * Write/label all samples throughout the process so that Client and sample numbers can be tracked. * Perform calculations, checking and interpretation of results where applicable. * Track status of designated tests as assigned to ensure Client turn around time commitments are met and inform supervisor of non compliance. * Assist other departmental personnel with analysis tasks so that testing can proceed according to specified time limits. * Update logbooks, transfer data and maintain records, including quality records for the specified tests, notify supervisor of any non compliant results. * Perform necessary housekeeping duties in a timely manner, keeping the work areas and equipment clean and sanitized. * Must participate in cleaning schedule and maintain retain samples as required. * Train analysts where required and participate in the training programs. * Perform necessary preventative maintenance on instrumentation according to identified schedules. * Clean and prepare glassware for future analysis use. * Ensure material/supplies are maintained and available for the next analysis including preparation of reagents where applicable. * Coordinate with other department personnel with analysis tasks to maintain smooth flow of work * Maintain knowledge of Laboratory Information Management System (LIMS) that is required to complete job responsibilities. * Support corporate quality and continuous improvement process,including participation in monitoring of quality parameters as assigned, and performance of necessary tasks related to quality control parameters for the test being performed. * This position has the responsibilities and authority to identify departures from the quality system or test procedures and document such observations in accordance with the prescribed complaint system and supervisor is notified. * Responsibility to support laboratory management in the implementation, maintenance, and improvement of the quality management system. * Adhere to all safety policies. * Perform other related tasks as needed YOUR PROFILE The incumbent must have a basic knowledge of chemistry to accurately perform testing procedures and obtain accurate results. Profile: * Associates degree and one or more years of experience, or Bachelors degree. Required skills: * This position requires a basic level of knowledge in both wet and instrumental chemistry procedures to perform analysis on samples. * Analytical skills are essential to complete analysis procedures and determine the concentration of the microorganism. * A general knowledge of the Laboratory Information Management System is required to process client data. * Physical dexterity is required for manipulating samples. Work Environment: The incumbent works in a laboratory setting with proper lighting and temperature control. Occasional exposure to laboratory fumes, chemicals, and materials will occur when in the laboratory. Safety equipment of gloves, laboratory coat and eyeglasses may need to be worn depending on the testing process. The incumbent may use the autoclave daily to complete the analysis process. Continuous lifting of analysis materials weighing up to 50 pounds are necessary to transport media materials. The incumbent can expect extended time spent in a standing position. The incumbent should be able to detect slight variation in shades of colors. WHY JOIN US? * Because you would contribute to an inspiring Public Health purpose, supported by long-term and visionary shareholders. * Because you would have an impact on our strategic pillars that build on 50 years of experience and expertise. * Because you would be part of a community of an enthusiastic and skilled group of people who love co-building together and serving a purpose bigger than them. * Because you would be welcome as you are, in a diverse and open-minded environment that is rich in our singularities and differences. * Because you would grow in an international group of more than 8200 fantastic team members, with plenty of opportunities to learn and share. Ready for the journey? To apply please click on 'Apply now' button

Laboratory Analysts conduct testing under supervised conditions in accordance with established procedures. Successful lab analysts are people who enjoy conducting tests following written instructions, who pay close attention to detail to make sure everything is done correctly, and who have high standards of personal integrity so that they deliver high-quality results. Education/Experience: Required * High school diploma or GED required * No experience necessary. If you are willing to learn and put in the work, we will train you! Preferred Experience (not required) * Bachelors Degree in a relevant Life Science * Microbiology, Biology, Chemistry, Biochemistry, Biotechnology, or similar * Laboratory experience Shifts: * Shifts are 8 hours per day unless otherwise specified * Shift Start Times (specifics will be coordinated during the interview and offer process) * Shift Start: 8/9am * Days worked: Monday through Friday You are more likely to succeed in this role if you: * Enjoy following written instructions to achieve a repeatable result. * Pay close attention to detail and pride yourself on the quality and accuracy of your work. * Are a hard worker who thrives in a fast-paced production environment. * Take interest in learning new and challenging things, and you come up to speed quickly. * Have high standards of honesty and integrity. You should Join Nelson Labs if you are looking for the following: * A connection to our powerful mission of Safeguarding Global Health. We test products every day that are used in life-saving situations around the globe by hundreds of millions of people each year. * Opportunities to grow and develop. This is a place you can advance your career! * A sense of belonging with your team. Camaraderie matters here! * A supervisor who cares about you, supports you, and has your back. * A chance to have your voice listened to and heard. Feedback is an important part of our culture. The Lab Analyst's essential duties include: * Performing laboratory testing in a supervised environment. * Carefully following established testing and traceability procedures and regulatory requirements. * Recording data from testing results, paying close attention to detail. * Communicating any unexpected issues that arise during testing to lab leadership. * Participating in reviews of quality events to understand root cause of unexpected results or deviations. * Providing additional support to the lab as needed (order supplies, review documents, other duties as assigned). Physical Requirements: The physical demands described here are a representation of those that must be met to perform the essential job functions: * Required to sit 15% of the day, stand and traverse 75% of the day to various office and lab locations and 10% of the day working at a computer. * Bending, stooping, crouching, crawling and climbing. * Must be able to work while wearing personal protective equipment such as safety glasses, goggles, face shields, gloves, lab coats and personal protective equipment deemed necessary to protect testing and to protect employees from various solutions, wastes, etc. * Must be able to lift and/or move up to 45 pounds. Sotera Health offers a competitive benefits package that includes: * Medical, Rx, Dental, Vision, Disability, Life Insurance, Health Savings and Flexible Spending Accounts * 401(k) program with Company match that immediately vests * Paid holidays, vacation and sick time * Free financial planning assistance * Paid parental leave * Education assistance * Voluntary benefits including Critical Illness, Accident, Hospital Indemnity and Pet Insurance * Employee Assistance Program (EAP)

The Sterility Assurance Laboratory Analyst conducts studies following established approved procedures and under the supervision of the Study Director or Department Manager. Additionally, the Sterility Assurance Laboratory Analyst performs their work in a Cleanroom, isolator or walk-in incubator environment, records data concurrently, maintains traceability of samples throughout testing and notifies the Study Director of any unforeseen circumstances or events that occur during testing. Laboratory Analysts conduct testing under supervised conditions in accordance with established procedures. Successful lab analysts are people who enjoy conducting tests following written instructions, who pay close attention to detail to make sure everything is done correctly, and who have high standards of personal integrity so that they deliver high-quality results. Education/Experience: High school diploma or GED required. No experience necessary. If you are willing to learn and put in the work, we will train you! Capability to work within a Sterile Cleanroom environment adhering to all safety and training protocols Wearing required sterile clothing: full body garment/gown, hood, googles, gloves, shoe covers, etc. Adhering to decontamination protocols before entering and upon exiting the Cleanroom setting Conducting tests within Cleanroom for periods of 4-6 hours depending on required tests and project needs Shifts: Shifts are 8 hours per day unless otherwise specified General Shift Start Times (specifics will be coordinated during the interview and offer process) Early Day Shift Start: between 5:30am-7:30am *Hours worked inside the Cleanroom pay an additional 20% on top of that! You are more likely to succeed in this role if you: Enjoy following written instructions to achieve a repeatable result. Pay close attention to detail and pride yourself on the quality and accuracy of your work. Are a hard worker who thrives in a fast-paced production environment. Take interest in learning new and challenging things, and you come up to speed quickly. Have high standards of honesty and integrity. You should Join Nelson Labs if you are looking for the following: A connection to our powerful mission of Safeguarding Global Health . We test products every day that are used in life-saving situations around the globe by hundreds of millions of people each year. Opportunities to grow and develop. This is a place you can advance your career! A sense of belonging with your team. Camaraderie matters here! A supervisor who cares about you, supports you, and has your back. A chance to have your voice listened to and heard. Feedback is an important part of our culture. The Lab Analyst's essential duties include: Performing laboratory testing in a supervised environment. Carefully following established testing and traceability procedures and regulatory requirements. Recording data from testing results, paying close attention to detail. Communicating any unexpected issues that arise during testing to lab leadership. Participating in reviews of quality events to understand root cause of unexpected results or deviations. Providing additional support to the lab as needed (order supplies, review documents, other duties as assigned). Physical requirements: Employee must stand and walk for 80% of the day; sit at a desk for 20%, 15% of sitting time is spent working on the computer. Employee must be able to lift a minimum of 25 lbs. Employee must be able to perform duties while wearing cleanroom garments and/or when exposed to 35 degree C heat. Sotera Health offers a competitive benefits package that includes: Medical, Rx, Dental, Vision, Disability, Life Insurance, Health Savings and Flexible Spending Accounts 401(k) program with Company match that immediately vests Paid holidays, vacation and sick time Free financial planning assistance Paid parental leave Education assistance Voluntary benefits including Critical Illness, Accident, Hospital Indemnity and Pet Insurance Employee Assistance Program (EAP)

HealthTrust Workforce Solutions HCA is seeking a travel Cath Lab Technologist for a travel job in Salt Lake City, Utah. Job Description & Requirements Specialty: Cath Lab Technologist Discipline: Allied Health Professional Start Date: 04/14/2025 Duration: 13 weeks 40 hours per week Shift: 10 hours, days Employment Type: Travel ACLS, BLS Required 7:00AM-5:30PM-Days (893191) About HealthTrust Workforce Solutions HCA At HealthTrust Workforce Solutions, healthcare is not just about the four walls of a facility but about the people who provide and receive care. Our focus is on empowering healthcare professionals to deliver exceptional patient experiences by providing them with the necessary skills, tools, and support. We partner with healthcare facilities nationwide to ensure that the right professionals are in the right roles. We prioritize our clinicians by giving them a voice and access to opportunities to fulfill their mission of improving lives by providing quality patient care. We are committed to our core values of Trust, Innovation, Adaptability, Courage, and Accountability. We are dedicated to positively impacting the healthcare industry by providing first-priority access to more than 200,000 jobs nationwide to our healthcare professionals. Join us and be part of the HealthTrust family, where you can make a difference every day. We embrace our changing environment, and we maintain a culture that has a rich tradition of transforming itself to meet the challenges of the future. MISSION STATEMENT While putting great people in the right roles is essential, our mission is far greater. We want our clinicians to be part of the HealthTrust family, where healthcare professionals have a voice and are empowered with the right tools and opportunities to fulfill their personal mission of improving lives. Plus, as a preferred partner to thousands of top-performing hospitals, we provide our healthcare professionals with first-priority access to more than 200,000 jobs nationwide. Benefits Dental benefits Vision benefits Referral bonus Continuing Education Life insurance

Avarint is a wholly owned subsidiary of CUBRC Inc. Pending Contract Award*** Avarint's Chemical Sciences Group is seeking a Chemist to support an experimental team conducting Research, Development, Test and Evaluation (RDT&E) at Dugway Proving Ground, UT. Primary duties will include: Planning and executing RDT&E projects with minimal guidance to include designing experiments, collecting and analyzing data, and troubleshooting technical problems. Working with highly toxic chemicals and materials and providing technical expertise and support to the development of Standard Operating Procedures (SOPs). Operating, maintaining, and troubleshooting analytical test equipment (GC, GC-MS, and/or LC-MS/MS) and working closely with project managers to adjust methods to meet project objectives. Reviewing and continuously improving the QA/QC program to ensure that all reported data is accurate, complete, reliable,e and of high confidence. Developing analysis reports that include methods, procedures, and analytical data including interpretation of results and annotating the file documentation; and performing technical and/or administrative reviews of files, reports, data sets, results, and conclusions. Maintaining a safe laboratory work environment in accordance with all documented laboratory procedures. The position also requires that the selected candidate possess: Strong hands-on laboratory skills with respect to GC-MS and/or LC-MS/MS instrument operation and sample analysis. Excellent organizational skills and communication skills (oral and written) and the ability to appropriately communicate with colleagues, management and clients to plan and execute duties. Deep attention to detail and the flexibility and ability to work both independently and as part of a team. Requirements THE FOLLOWING REQUIREMENTS MUST BE MET TO BE CONSIDERED FOR THIS POSITION: Minimum Qualifications B.S. in Chemistry, Analytical Chemistry, Biochemistry or other related physical science or engineering discipline with a minimum of two (2) years of relevant laboratory experience; or equivalent combination of education and experience. Experience with Microsoft Office software including MS Word, Outlook, Excel and PowerPoint. Experience and proficiency with gas chromatography, GC-MS and/or LC-MS/MS. Ability to obtain and maintain a DoD Secret security clearance. U.S. citizenship. A medical examination will be required to ensure ability to perform duties and wear personal protective equipment. THE FOLLOWING REQUIREMENTS ARE DESIRED BUT NOT REQUIRED FOR THIS POSITION: An active DoD security clearance (S or TS). Experience working with Miniature Chemical Agent Monitoring Systems (MINICAMS) for workplace air monitoring during test operations. Experience with Microsoft Office software (Access, Project, Outlook, SharePoint and Teams). Experience in contract research, working for the federal government and/or private organizations. Why Avarint: 401K - No waiting period. 100% vested on the date of hire. 3% company contribution in the first year of employment, company contribution increases over time. The employee is not required to contribute to the plan to receive Avarint contribution. Health Insurance - No waiting period - competitive costs. Dental and vision insurance after 6 months - Employer-paid benefit for employees and dependents. Life Insurance after 6 months - Employer paid benefit for the employee. Generous paid time off, unlimited sick time, and 9 paid holidays. The candidate will be subject to a government security investigation and must meet eligibility requirements for access to classified information. U.S. citizenship is required. The position requires participation in a Chemical Personnel Reliability Program (CPRP), administered by the U.S. Army. A medical examination will be required to ensure the ability to perform duties and wear personal protective equipment. The candidate will also be required to comply with a Drug Testing Program. Avarint is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status.

Mindlance is a national recruiting company which partners with many of the leading employers across the country. Feel free to check us out at ************************* Duration: 6+ month Job Description: Under general supervision, performs cGMP laboratory analyses of Finished products and in process materials. Performs stability testing for Finished products. Performs maintenance and calibration of analytical instruments. Minimum Qualifications: Bachelor's Degree in Science or related science field from an accredited college or university and one (1) year related laboratory experience or an equivalent combination of education and experience. Experience and Skills: •Usage of GC and HPLC chromatographic equipment, as well as UV/VIS, and FTIR operation methods and techniques. •Business, scientific and personal computer hardware and software applications. •Business English usage, spelling, grammar and punctuation. •Wet Chemistry and Chemistry related to sampling methods, quality control systems, analysis and documentation practices and procedures. •Knowledge of or ability to learn FDA, cGLP, cGMP, USP, EP and SOP or other applicable regulatory and safety compliance guidelines. •Performing testing accurately and precisely. •Responding to routine inquiries from management, employees and regulatory agencies. •Communicating clearly and concisely, both orally and in writing. •Managing multiple projects, duties and assignments. •Establishing and maintaining cooperative working relationships with others. Essential functions include: *Carries out responsibilities in accordance with the organization's policies, procedures and state, federal and local laws. *Operates general analytical instruments during the testing of finished products using HPLC, UPLC, GC-FID, UV-VIS, FTIR, automatic titrators, Dissolution Apparatus *Performs physical testing such as viscosity testing, Instron testing, and microscopy . *Performs wet chemistry tests on samples such as pH, titration, gravimetry and prepares standard, sample, and buffer solutions as required by test methods and performs all necessary calculations associated. *Labels, transcribes and records documentation such as report sheets and laboratory notebooks as required by SOPs. *Cleans, maintains and calibrates laboratory equipment to ensure compliance with current Good Manufacturing Procedures (cGMP). *Meets project deadlines and performance standards as assigned. *Complies with all Company policies and procedures, including safety rules and regulations *Performs investigations and troubleshooting of analytical test methods and lab instruments. *Performs investigation and writes reports on findings, conclusion and identify corrective actions/preventative actions. *Carries out quantitative and qualitative analyses in support of method comparisons, method transfers, method validations, product in-use study. *Train junior level scientist and technician and participate in identifying process to improve efficiency in laboratory testing. *Assist in organizing, staging and pulling samples for stability studies. *Assist in creating database for stability sample pull, staging sample and test schedules. *Performs related duties as assigned. Qualifications Minimum Qualifications: Bachelor's Degree in Science or related science field from an accredited college or university and one (1) year related laboratory experience or an equivalent combination of education and experience. Experience and Skills: •Usage of GC and HPLC chromatographic equipment, as well as UV/VIS, and FTIR operation methods and techniques. •Business, scientific and personal computer hardware and software applications. •Business English usage, spelling, grammar and punctuation. •Wet Chemistry and Chemistry related to sampling methods, quality control systems, analysis and documentation practices and procedures. •Knowledge of or ability to learn FDA, cGLP, cGMP, USP, EP and SOP or other applicable regulatory and safety compliance guidelines. •Performing testing accurately and precisely. •Responding to routine inquiries from management, employees and regulatory agencies. •Communicating clearly and concisely, both orally and in writing. •Managing multiple projects, duties and assignments. •Establishing and maintaining cooperative working relationships with others. Additional Information All your information will be kept confidential according to EEO guidelines.

Neurodegenerative diseases are one of the largest medical challenges of our time. Denali Therapeutics is a biotechnology company dedicated to developing breakthrough therapies for neurodegenerative diseases through our deep commitment to degeneration biology and principles of translational medicine. Denali is founded on the collaboration of leading scientists, industry experts, and investors who share the vision that scientific discovery energetically applied to translational medicine is the key to delivering effective therapies to patients. We invite you to consider an opportunity with Denali to help achieve our goal of delivering meaningful therapeutics to patients. This role will play a key role in executing and reports analytical/chemistry test methods for raw materials, drug substance and drug product for large molecule clinical and commercial products. Key Accountabilities/ Core Job Responsibilities: Performs implementation and execution of routine and ad hoc chemical and analytical testing for raw materials and large molecule drug substance and drug product. Supports the qualification and implementation of USP/EP methods and product specific methods as part of new product introduction and technology transfer. Supports stability testing of drug substance and drug product for all timepoints and conditions. Supports quality events such as CAPA, Change Control, Deviations, and LIR/OOS as subject matter expert for QC Chemistry Generates, analyzes, and reports data and takes appropriate action Works within LabWare LIMS for execution of methods, data trending and report issuance. Reviews documentation for product disposition, generates COA/COC and batch summary reports Works with accuracy, urgency and a continuous improvement perspective Provides flexible support for on-call or outside normal business hours if required Qualifications/Skills: BS in Chemistry or equivalent science 4+ years of experience working in GMP regulated chemistry laboratory Large molecule experience preferred Familiarity with GMP regulations Knowledge of current USP/Ph. Eur./FDA/ISO/GMP standards and guidance Ability to work with independently Build productive relationships with internal teams and external sources Well-developed verbal and written communication skills Excellence in execution through accuracy, right first time and a proactive nature Physical requirements- must be able to put on specialized gowning, lift and manipulate items over 25 lbs, climb ladders, stand for multiple hours at a time Strong collaboration and project management skills Familiar with Master Control and LabWare LIMS Compensation for the role will depend on a number of factors, including a candidate's qualifications, skills, competencies, and experience. Denali offers a competitive total rewards package, which includes a 401k, healthcare coverage, ESPP and a broad range of other benefits. Learn more at ****************************************** This compensation and benefits information is based on Denali's good faith estimate as of the date of publication and may be modified in the future.This compensation and benefits information is based on Denali's good faith estimate as of the date of publication and may be modified in the future. Denali is committed to its core company value of unity by creating a diverse and inclusive environment. We are proud to be an equal opportunity employer and do not discriminate against any employee or applicant for employment because of race, color, sex, age, national origin, religion, sexual orientation, gender identity and/or expression, status as a veteran, basis of disability, or any other federal, state, or local protected class.

Certified Group is committed to delivering expert solutions and quality testing our customers can feel confident in - on time, every time - so the world can trust in what it consumes. As a leading North American provider of laboratory testing, regulatory consulting, and certification & audit services, Certified Group includes Food Safety Net Services (FSNS), FSNS Certification & Audit, Certified Laboratories, EAS Consulting Group, and Labstat International Inc. Certified Group provides analytical testing and regulatory guidance services in the food & beverage, dietary supplements & NHP, cosmetics, OTC, personal care, tobacco, nicotine, cannabis, and hemp industries. We have embarked on an important journey to unify and strengthen our culture by living these core values: Start with the Customer, Drive to Deliver, Commit to Safety and Quality, and Believe in the Team - including believing in you. We are currently looking for a Pathogen Lab Analyst to join our growing team! Job Summary: Perform analytical and microbiological testing of food products, ingredients, and environmentals. The position performs the application and evaluation of approved microbiological techniques and methodologies. Essential Responsibilities: * Accurately perform and read test results and notify Laboratory Management of deviations * Prepare and analyze samples for indicator organisms, pathogens, and chemistries * Apply aseptic/microbiological techniques in daily workload * Report inventory and expendable supplies/materials needed for testing requirements * Provide routine preventive maintenance by daily cleaning, sanitizing, trash disposal, and equipment quality control * Assist in quality duties to by taking incubator temperatures, inoculating control organisms, running media controls, etc. * Pursue an assigned series of processes, procedures, or techniques in accordance with FSNS policies/procedures and customer requirements * Maintain a high degree of technical competence by reading scientific journals, attending professional workshops, and being aware of food industry issues and trends * Perform all activities in a neat, safe, hygienic, and efficient manner * Share information in an open and timely manner * Assisting with managing priorities and schedule such that individual goals as well as team goals are achieved with encouraged participation in the Food Safety Net Services Team * Responsible for the safety of oneself and others working within their area Education & Experience: * Associate degree in Life Science or related field with two or more years of laboratory experience, preferred * Two or more years of experience in a commercial food-testing or analytical laboratory * Or equivalent combination of education and experience * Working knowledge of aseptic sampling technique, automated lab equipment, and acceptable methods and procedures * Familiarity with GLP, OSHA guidelines, FDA, BAM, APHA, ISO, and USP methods and procedures * Broad knowledge of concepts, practices, and procedures of a food testing laboratory * Ability to travel when necessary Physical Demands/Work Environment: * Dexterity of hands and fingers to operate a computer keyboard, mouse and to handle other communications/computer components * Potential exposure to odors, fumes, airborne particles, hazardous chemicals, and microbiological pathogens * Noise level varies from quiet to loud * Temperature varies from hot to cold * Interactive and fast-paced team oriented tasks * Overnight Travel is required at the discretion of management * Occasionally lift and/or move up to 25 pounds * Color vision and depth perception Benefits: * Progressive 401k Retirement Savings Plan * Employer Paid Short- Term and Long-Term Disability, and Life Insurance * Group Medical * Tuition Reimbursement * Flexible Spending Accounts * Dental * Paid Holidays and Time Off Certified Group values diversity in its workforce. The company is firmly committed to a policy of Equal Opportunity and will administer its policies in a manner that treats each employee and applicant for employment on the basis of merit. Certified Group will take affirmative action to seek out qualified applicants without regard to race, color, religion, sex, national origin, age, handicap, or veteran status.

Laboratory Analysts conduct testing under supervised conditions in accordance with established procedures. Successful lab analysts are people who enjoy conducting tests following written instructions, who pay close attention to detail to make sure everything is done correctly, and who have high standards of personal integrity so that they deliver high-quality results. Education/Experience: Required High school diploma or GED required No experience necessary. If you are willing to learn and put in the work, we will train you! Preferred Experience (not required) Bachelors Degree in a relevant Life Science Microbiology, Biology, Chemistry, Biochemistry, Biotechnology, or similar Laboratory experience Shifts: Shifts are 8 hours per day unless otherwise specified Shift Start Times (specifics will be coordinated during the interview and offer process) Shift Start: 8/9am Days worked: Monday through Friday You are more likely to succeed in this role if you: Enjoy following written instructions to achieve a repeatable result. Pay close attention to detail and pride yourself on the quality and accuracy of your work. Are a hard worker who thrives in a fast-paced production environment. Take interest in learning new and challenging things, and you come up to speed quickly. Have high standards of honesty and integrity. You should Join Nelson Labs if you are looking for the following: A connection to our powerful mission of Safeguarding Global Health . We test products every day that are used in life-saving situations around the globe by hundreds of millions of people each year. Opportunities to grow and develop. This is a place you can advance your career! A sense of belonging with your team. Camaraderie matters here! A supervisor who cares about you, supports you, and has your back. A chance to have your voice listened to and heard. Feedback is an important part of our culture. The Lab Analyst's essential duties include: Performing laboratory testing in a supervised environment. Carefully following established testing and traceability procedures and regulatory requirements. Recording data from testing results, paying close attention to detail. Communicating any unexpected issues that arise during testing to lab leadership. Participating in reviews of quality events to understand root cause of unexpected results or deviations. Providing additional support to the lab as needed (order supplies, review documents, other duties as assigned). Physical Requirements: The physical demands described here are a representation of those that must be met to perform the essential job functions: Required to sit 15% of the day, stand and traverse 75% of the day to various office and lab locations and 10% of the day working at a computer. Bending, stooping, crouching, crawling and climbing. Must be able to work while wearing personal protective equipment such as safety glasses, goggles, face shields, gloves, lab coats and personal protective equipment deemed necessary to protect testing and to protect employees from various solutions, wastes, etc. Must be able to lift and/or move up to 45 pounds. Sotera Health offers a competitive benefits package that includes: Medical, Rx, Dental, Vision, Disability, Life Insurance, Health Savings and Flexible Spending Accounts 401(k) program with Company match that immediately vests Paid holidays, vacation and sick time Free financial planning assistance Paid parental leave Education assistance Voluntary benefits including Critical Illness, Accident, Hospital Indemnity and Pet Insurance Employee Assistance Program (EAP)

The Sterility Assurance Laboratory Analyst conducts studies following established approved procedures and under the supervision of the Study Director or Department Manager. Additionally, the Sterility Assurance Laboratory Analyst performs their work in a Cleanroom, isolator or walk-in incubator environment, records data concurrently, maintains traceability of samples throughout testing and notifies the Study Director of any unforeseen circumstances or events that occur during testing. Laboratory Analysts conduct testing under supervised conditions in accordance with established procedures. Successful lab analysts are people who enjoy conducting tests following written instructions, who pay close attention to detail to make sure everything is done correctly, and who have high standards of personal integrity so that they deliver high-quality results. Education/Experience: * High school diploma or GED required * Capability to work in a production laboratory setting under deadlines while maintaining test quality and accuracy * Aptitude to learn repeatable testing procedures and scientific protocols * Capability to work within a Sterile Cleanroom environment adhering to all safety and training protocols * Wearing required sterile clothing: full body garment/gown, hood, googles, gloves, shoe covers, etc. * Adhering to decontamination protocols before entering and upon exiting the Cleanroom setting * Conducting tests within Cleanroom for periods of 4-6 hours depending on required tests and project needs Shifts: * Shifts are 8 hours per day unless otherwise specified * Shift Start Times (specifics will be coordinated during the interview and offer process) * Shift Start: 2/3pm * Days worked: Monday through Friday * *Our Swing Shift pays an additional 15% per hour on top of your hourly rate * Hours worked inside the Cleanroom pay an additional 20% on top of that! You are more likely to succeed in this role if you: * Enjoy following written instructions to achieve a repeatable result. * Pay close attention to detail and pride yourself on the quality and accuracy of your work. * Are a hard worker who thrives in a fast-paced production environment. * Take interest in learning new and challenging things, and you come up to speed quickly. * Have high standards of honesty and integrity. You should Join Nelson Labs if you are looking for the following: * A connection to our powerful mission of Safeguarding Global Health. We test products every day that are used in life-saving situations around the globe by hundreds of millions of people each year. * Opportunities to grow and develop. This is a place you can advance your career! * A sense of belonging with your team. Camaraderie matters here! * A supervisor who cares about you, supports you, and has your back. * A chance to have your voice listened to and heard. Feedback is an important part of our culture. The Lab Analyst's essential duties include: * Performing laboratory testing in a supervised environment. * Carefully following established testing and traceability procedures and regulatory requirements. * Recording data from testing results, paying close attention to detail. * Communicating any unexpected issues that arise during testing to lab leadership. * Participating in reviews of quality events to understand root cause of unexpected results or deviations. * Providing additional support to the lab as needed (order supplies, review documents, other duties as assigned). Physical requirements: Employee must stand and walk for 80% of the day; sit at a desk for 20%, 15% of sitting time is spent working on the computer. Employee must be able to lift a minimum of 25 lbs. Employee must be able to perform duties while wearing cleanroom garments and/or when exposed to 35 degree C heat. Sotera Health offers a competitive benefits package that includes: * Medical, Rx, Dental, Vision, Disability, Life Insurance, Health Savings and Flexible Spending Accounts * 401(k) program with Company match that immediately vests * Paid holidays, vacation and sick time * Free financial planning assistance * Paid parental leave * Education assistance * Voluntary benefits including Critical Illness, Accident, Hospital Indemnity and Pet Insurance * Employee Assistance Program (EAP)