Microbiologist jobs in Minnesota

Microbiologist New Ulm Plant * Full benefit package (Medical, Dental, Vision, HAS) * Company matched 401K (6%) * Additional perks: Pet Insurance, Employee Assistance Program (EAP), access to shop at the Company Store. * Paid vacation, sick and major holidays * Microbiologist positions begin at $32.69. * Annual bonus (potential 3.5% annual salary). * $1.00/hr shift premium Work Schedule: Primarily 1st/ Day shift. Plant & Community Overview: Plant Overview: * The Kraft Heinz Plant in New Ulm has been a workplace of choice in the community since its opening in 1955. Current products include Velveeta, Velveeta Mini-Block, Kraft Deli-Deluxe, and Foodservice for popular restaurant chains. * 400 Hourly Employees. * 23 Salaried Employees. * Average tenured employee is 12 years of service. * Over 125 employees have more than 20 years of service. * There is over 5,000 years of experience in the New Ulm Plant! Community Overview: Welcome to our New Ulm Community! Scope of Job: The Microbiologist is responsible for overseeing microbiological testing and ensuring compliance with Kraft/Heinz standards and all legal regulations at the New Ulm factory. Responsible for managing the Environmental Monitoring Program, Plant Water Testing, Equipment Swabs, and Finished Product Pathogen testing. This individual works closely with Corporate Food Safety Micro on all aspects of required testing and when out of specification results are obtained. Primary Responsibilities: * Performs daily microbiological analysis on finished products and raw materials, including SPC, Coliform, Yeast and Mold testing. * Prepare dilution bottles used for testing finished product and liquid loads. * Conducts microbiological analysis on environmental swabs and plates, including clean equipment swabs, continuous swabs, employee fingerplates, compressed air, and air exposures and reports results to supervisors and managers. * Develops and initiates new micro testing for new production in the plant, including creating programs for recording and reporting results. * Ensures compliance with corporate, plant, and legal guidelines for microbiological testing and standards. * Records and reports work accurately, updating weekly out-of-standard graphs and sending them to relevant managers and supervisors. * Notifies Compliance Manager and Quality Manager of out-of-spec results or negative trends. * Participates in quarterly Proficiency testing program to monitor accuracy and proficiency of microbiological testing. * Prepares analysis media, swabs, and plates on a timely basis. * Cleans, sanitizes, and monitors a sterile environment for performing tests. * Records and monitors autoclave for sterilization. * Records and monitors incubators and oven temperatures to ensure proper analysis. * Performs monthly calibration checks on pipettes. * Manages inventory and orders microbiological supplies using SRM. * Responsible for Environmental swabbing and reporting weekly results and trends to the management team. * Coordinates all Project Forward meetings. * Manages the Water Quality Program, including taking water samples, sending out for testing, and troubleshooting issues. * Collects samples for non-routine microbiologic testing and arranges for testing with external laboratories. * Develop and initiate with management any new micro testing for new production and develop new programs for recording and reporting results. * Supervises and directs the work of Lab Analysts, Sanitation associates, and Quality Supervisors as needed for micro purposes. * Provides yearly training on swab procedures to Lab Analysts, Sanitation associates, and Quality Supervisors. * Schedules and conducts finished product pathogen testing. * Records microbiological test results in SAP and reports and trends results. * Performs month-end reporting for PEM swabs, start-up swabs, air exposures, and finger plates. * Monitors lab R.O. water system and contacts vendor for filter replacement/maintenance. * Participates in 3rd party, Kraft Heinz, and customer audits covering environmental monitoring and microbiological programs. * Works non-core hours and/or weekends as needed to ensure compliance and resolve issues. * Performs special plating, swabs, and bacti programs upon request of supervisor. * Responsible for recording ingredient results. * Responsible for the annual micro budget and ensuring the associated PO's are created for outside laboratory testing to ensure invoices get paid. * The Microbiologist works with live and potentially hazardous cultures. Caution must be used to prevent the spread of these microorganisms to employees and/or the plant. Due to the danger of live cultures, the Microbiologist must sanitize the micro area daily wear proper PPE and follow good Lab practices. * Operates Vidas, autoclave, ovens, incubators, and stomacher. Working Conditions: Must wear a Lab coat, booties and Safety glasses when working in Bacti prep room. Handles materials up to15 lbs or less frequently or up to 45 lbs infrequently. When performing pathogen (Listeria and Salmonella) testing, rubber gloves must also be worn. This is a dangerous and infectious substance. Working temperatures range from 35 to 75 degrees. Safety hazards are present when working with the autoclave (pressure of 15 lbs steam temperatures of 250 degrees Celsius). Work is done in all production areas where microbiologist retrieves samples, around and under machinery in slippery and wet conditions. Preferred Qualifications: * High School diploma required. * Degree in related field or related lab experience preferred. * Must have experience with personal computers and software. * Strong verbal, written, analytical, and interpersonal skills needed. * Strongly recommended being able to work with very minimal supervision and use own judgment. * Must develop good knowledge of the plant to lead plant wide microbiological programs and in problem solving. Training: The Microbiologist will have a three-phase training period; 30, 60, and 90 days. An evaluation will be done after each phase. The successful Microbiologist will consistently demonstrate mastery of key competencies throughout all phases of training, ensuring a strong foundation for success in the role. Qualifications: * High School Diploma/GED Preferred. * Previous Manufacturing Experience Preferred. * Seeking individuals who work well with teams, are goal oriented, and enjoy satisfaction in performing a job well done. * Must be able to lift 50 pounds frequently, and up to 100 pounds infrequently, with or without reasonable accommodations. #INDMFGH Benefits: Coverage for employees (and their eligible dependents) through affordable access to healthcare, protection, and saving for the future, we offer plans tailored to meet you and your family's needs. Coverage for benefits will be in accordance with the terms and conditions of the applicable plans and associated governing plan documents. Wellbeing: We offer events, resources, and learning opportunities that inspire a physical, social, emotional, and financial well-being lifestyle for our employees and their families. You'll be able to participate in a variety of benefits and wellbeing programs that may vary by role, country, region, union status, and other employment status factors, for example: * Physical - Medical, Prescription Drug, Dental, Vision, Screenings/Assessments * Social - Paid Time Off, Company Holidays, Leave of Absence, Recognition, Training * Emotional - Employee Assistance Program , Wellbeing Programs, Family Support Programs * Financial - 401k, Life, Accidental Death & Dismemberment, Disability Location(s) New Ulm Plant Kraft Heinz is an Equal Opportunity Employer that prohibits discrimination or harassment of any type. All qualified applicants are considered for employment without regard to race, color, national origin, age, sex, sexual orientation, gender, gender identity or expression, disability status, protected veteran status, or any other characteristic protected by law. Applicants who require an accommodation to participate in the job application or hiring process should contact ***********************.

Vantive is a vital organ therapy company on a mission to extend lives and expand possibilities for patients and care teams everywhere. For 70 years, our team has driven meaningful innovations in kidney care. As we build on our legacy, we are deepening our commitment to elevating the dialysis experience through digital solutions and advanced services, while looking beyond kidney care and investing in transforming vital organ therapies. Greater flexibility and efficiency in therapy administration for care teams, and longer, fuller lives for patients- that is what Vantive aspires to deliver. We believe Vantive will not only build our leadership in the kidney care space, it will also offer meaningful work to those who join us. At Vantive, you will become part of a community of people who are focused, courageous and don't settle for the mediocre. Each of us is driven to help improve patients' lives worldwide. Join us in advancing our mission to extend lives and expand possibilities. Your Role The Microbiologist III will report to the MN Microbiology Laboratory Manager and be responsible for the laboratory testing including but not limited to microbiological testing, moist heat sterilization evaluation and disinfection testing. What you will be doing Perform disinfection and cleaning of reusable devices. Evaluating system designs for areas of risk for cleaning and disinfection, support experiments to evaluate the efficacy of the disinfection and providing recommendations for disinfectants and designing disinfection processes. Work with product development teams, product design owners, contract testing laboratories and manufacturing QA/QC laboratory personnel to complete required tasks. Support re-qualification for sterilization and microbiological test methods, internally and at manufacturing sites. Responsible for helping design and lead testing on biofilms. Designing biofilm experiments (including biofilm controls), operating the biofilm reactors, and evaluating biofilm samples. Responsible for helping to evaluate various sterilization cycles and write reports. Track and document micro lab employees' lab training and ensure compliance; work with other site team lead to further establish overall process and tracking. Responsible for organizing and documenting weekly/monthly lab testing schedule and assigning responsibilities to team. Responsibilities include: Support Laboratory manager to maintain laboratory operations, including maintaining laboratory safety, improving operations and maintaining equipment. Assure laboratory and documentation is audit ready and team can effectively response to auditor inquiries. Assure appropriate investigations are conducted for laboratory failures and out of specifications. Assure the use of appropriate standards in laboratory testing. Supporting R&D projects through input on laboratory testing needs or the use of existing data to support products. Devising new approaches to complex problems through adaptations and modifications of standard technical principles. Where necessary implement new procedures to support the testing of Vantive products. Assuring all work complies with Vantive's Quality system and cGDP/cGMP practices. Providing regular updates to Sterility Assurance management. What you will bring B.S. with greater than 8 years of related experience Strong Microbiology background and experience required in the areas of: Biofilm testing including biofilm experimental design, growth methods, biofilm reactors and biofilm sampling techniques. Performing disinfection testing including knowledge of disinfectants, regulatory knowledge and experimental design, to demonstrate the disinfection efficacy for demonstrating product safety for reusable medical devices. Performing Bacterial Endotoxin Testing (BET) for new product development. Performing Moist heat sterilization of test materials as well as pharmaceutical and medical device test samples. Experience managing multiple simultaneous projects and work activities Experience leading and coordinating laboratory activities and drawing conclusions from laboratory lab data. Knowledge of renal therapies (Hemodialysis and Peritoneal Dialysis) Knowledge of GDP/GMP/GLP practices. Ability to convince management on courses of action with minimal assistance using both written and verbal methods. Project Management certification preferred Medical device testing Experience in laboratory methods, including: Bioburden Sterility testing Bacterial Endotoxin Test (BET) Sterile barrier / Container Closure Integrity (CCI) Antimicrobial testing Moist heat sterilization efficacy support Vantive is committed to supporting the needs for flexibility in the workplace. We do so through our flexible workplace policy which includes a minimum of 3 days a week onsite. This policy provides the benefits of connecting and collaborating in-person in support of our Mission. We understand compensation is an important factor as you consider the next step in your career. At Vantive, we are committed to equitable pay for all employees, and we strive to be more transparent with our pay practices. The estimated base salary for this position is $96-144,000 annually. The estimated range is meant to reflect an anticipated salary range for the position. We may pay more or less than of the anticipated range based upon market data and other factors, all of which are subject to change. Individual pay is based on upon location, skills and expertise, experience, and other relevant factors. This position may also be eligible for discretionary bonuses, and/or long-term incentive. For questions about this, our pay philosophy, and available benefits, please speak to the recruiter if you decide to apply and are selected for an interview. US Benefits at Vantive This is where your well-being matters. Vantive offers comprehensive compensation and benefits packages for eligible roles. Our health and well-being benefits include medical, dental and vision coverage that start on day one, as well as insurance coverage for basic life, accident, short-term and long-term disability, and business travel accident insurance. Financial and retirement benefits include the Aon Pooled Employer Plan (“Aon PEP”), Vantive's 401(k) retirement savings plan, to help you prepare for your future. The Aon PEP is designed to help improve retirement outcomes by providing retirement resources more efficiently. The plan offers a robust set of investment options, financial education, and a suite of resources to support your retirement goals. We also offer Flexible Spending Accounts, educational assistance programs, and time-off benefits such as paid holidays, paid time off ranging from 20 to 35 days based on length of service, family and medical leaves of absence, and paid parental leave. Additional benefits include commuting benefits, the Employee Discount Program, the Employee Assistance Program (EAP), and childcare benefits. Join us and enjoy the competitive compensation and benefits we offer to our employees. For additional information regarding Vantive's US Benefits, please speak with your recruiter or visit our Benefits site: Benefits | Vantive Equal Employment Opportunity Vantive is an equal opportunity employer. Vantive evaluates qualified applicants without regard to race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, protected veteran status, disability/handicap status or any other legally protected characteristic. Know Your Rights: Workplace Discrimination is Illegal Reasonable Accommodation Vantive is committed to working with and providing reasonable accommodations to individuals with disabilities globally. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please click on the link here and let us know the nature of your request along with your contact information. Form Link Recruitment Fraud Notice Vantive has discovered incidents of employment scams, where fraudulent parties pose as Vantive employees, recruiters, or other agents, and engage with online job seekers in an attempt to steal personal and/or financial information. To learn how you can protect yourself, review our Recruitment Fraud Notice.

LAB TECHNICIAN - MICROBIOLOGY LAB - RESEARCH & DEVELOPMENT (AUSTIN, MN) To save time applying, Hormel Foods does not offer sponsorship of job applicants for employment-based visas for this position at this time. Applicants must not now, or at any time in the future, require employer sponsorship for a work visa. Applicants must be authorized to work in the United States for any employer. RESPONSIBILITIES: Works with an intermediate degree of supervision and sometimes direct supervision. Performs assays in the general micro lab that include mostly non-pathogen organisms. Conducts Quality Control procedures for laboratory as assigned. Initiates and participates in Corrective Action Requests, Method Validation Projects, and Continuous Improvement Projects. Maintains Quality Control and ISO records as assigned. May assist with the administrative duties, such as, safety audits, obtaining COAs, and ordering supplies and chemicals. Performs other duties as assigned. QUALIFICATIONS: Required Successful completion of post-secondary education in a lab based, scientific discipline. Demonstrated basic lab skills including aseptic technique, quantitative and qualitative analysis. Strong math skills. Good computer skills including Outlook, Excel, Word, LIMS or equivalents. Demonstrated ability to perform independent or group work. Good communication skills. Must be capable of standing for extended periods of time, handle strong odors and may, on occasion, lift up to 50 lbs. Preferred 1-2 years of laboratory experience. Knowledge of Laboratory Quality Systems and Root Cause Analyses skills. Hormel Foods provides equal employment opportunities to applicants and employees without regard to race; color; sex; gender identity; sexual orientation; religious practices and observances; national origin; pregnancy, childbirth, or related medical conditions; status as a protected veteran or spouse/family member of a protected veteran; or disability. At Hormel Foods, base pay is one part of our total compensation package and is determined within a range. The base hiring pay range for this role is between $20.25 - $28.50 per hour, and your actual base pay within that range will depend upon a variety of factors including, but not limited to, job-related knowledge, skill set, level of experience, and geographic market location. Other components of Hormel Foods' total compensation package includes comprehensive medical, dental and vision coverage, discretionary annual merit increases, profit sharing, 401(k) with employer match, stock purchase plan, paid vacation, FREE two-year community/technical college tuition for children of employees, and more. For immediate consideration, apply online at: *************************** At Hormel we invite difference and diversity in all aspects. We offer a space of support, understanding, and community. We are committed to the journey! Learn more about our progress here: **********************************************************

Element has an opportunity for a Senior Microbiologist to join our Eagan, MN laboratory, which specializes in microbiological testing and analytical support for antimicrobial, pharmaceutical, medical device, and related regulated manufacturing and consumer product industries. The Senior Microbiologist performs and evaluates both custom and standardized testing that supports client needs; generates data while maintaining a high level of scientific integrity; assists in the review of test results, raw data, and Certificates of Analysis; designs and executes research and development (R&D) projects when implementing new methods or adapting current methods; maintains awareness of advances and changes in the test methodology; effectively communicates with management and others in the company to share information, offer ideas, and think creatively to effectively solve client testing problems to support registrations of new and novel antimicrobial products. In this role, you may also perform sterility and bioburden testing, environmental monitoring, and method qualifications. This position plays a key role in executing testing within a cGLP and ISO 17025 environment, maintaining data integrity, and ensuring results are scientifically sound, timely, and defensible. The Senior Microbiologist works closely with internal technical teams and external client partners and contributes directly to maintaining the high standards of quality and reliability that Element is known for. You can read a bit more about the work out Eagan lab does here: EMT Eagan Lab Page Responsibilities Performs and leads antimicrobial efficacy testing assays including standard methods and custom methods • May perform assays including bioburden, sterility testing, microbial enumeration, organism identification, endotoxin testing, and microbial limits testing. Conduct method development, qualification, verification, and validation activities in alignment with industry standards. May support environmental monitoring and cleanroom qualification programs, including surface, air, and personnel monitoring. Maintain accurate, compliant documentation within laboratory information and quality systems. Prepare test reports, review data, and communicate results clearly and professionally to internal and external partners. Participate in equipment maintenance, calibrations, and laboratory housekeeping to ensure safe and compliant operations. Assist with client technical transfers and onboarding of new test methods as needed. Ability to adapt standard laboratory techniques and tests to meet the demands of specific problems. Ability to make complex mathematical computations, use statistical techniques in the treatment of data, and interpret and apply findings. Work as an effective and proactive team-player; understands the importance of supporting the organization, customers, and other employees. Ability to maintain appropriate records for all facets of job. Able to use critical thinking, logic, and reasoning to identify the strengths and weaknesses of alternative solutions, conclusions, or approaches to problems. Able to communicate effectively in writing as appropriate for the needs of the audience. Able to manage work time, determine priorities, seek assistance when necessary, and complete projects within deadlines. Identifies complex problems and reviewing related information to develop and evaluate options and implement solutions independently. Able to plan, prioritize, coordinate, and manage work in a fast-paced environment. Able to work unsupervised, make complex level decisions independently, and solve problems effectively and creatively. Displays high levels of customer service, responding promptly and thoroughly to the inquiries and needs of individuals both internal and external to the organization, as applicable. Understand and maintain confidential nature of customer, organization and employee information. Show professional knowledge, proficiency and initiative in achieving goals and meeting standards Skills / Qualifications BS or MS in Microbiology, Biology, Medical Laboratory Science, or related discipline. 5 years of hands-on microbiology experience in a cGLP, ISO 17025, or regulated laboratory environment. Working knowledge of USP , , , , , , and related pharmaceutical microbiology standards. Demonstrated experience with aseptic technique and/or cleanroom operations. Reusable medical device testing is nice to have Strong documentation discipline and familiarity with GxP data integrity expectations. Ability to manage multiple projects while maintaining focus, accuracy, and compliance. Effective written and verbal communication skills, including the ability to interpret testing procedures and prepare clear technical documentation. #LI-TK1 Company Overview Element is one of the fastest growing testing, inspection and certification businesses in the world. Globally we have more than 9,000 brilliant minds operating from 270 sites across 30 countries. Together we share an ambitious purpose to ‘Make tomorrow safer than today'. When failure in use is not an option, we help customers make certain that their products, materials, processes and services are safe, compliant and fit for purpose. From early R&D, through complex regulatory approvals and into production, our global laboratory network of scientists, engineers, and technologists support customers to achieve assurance over product quality, sustainable outcomes, and market access. While we are proud of our global reach, working at Element feels like being part of a smaller company. We empower you to take charge of your career, and reward excellence and integrity with growth and development. Industries across the world depend on our care, attention to detail and the absolute accuracy of our work. The role we have to play in creating a safer world is much bigger than our organization. Diversity Statement At Element, we always take pride in putting our people first. We are an equal opportunity employer that recognizes diversity and inclusion as fundamental to our Vision of becoming “the world's most trusted testing partner”. All suitably qualified candidates will receive consideration for employment on the basis of objective work related criteria and without regard for the following: age, disability, ethnic origin, gender, marital status, race, religion, responsibility of dependents, sexual orientation, or gender identity or other characteristics in accordance with the applicable governing laws or other characteristics in accordance with the applicable governing laws.

Element has an opportunity for a Senior Microbiologist to join our Eagan, MN laboratory, which specializes in microbiological testing and analytical support for antimicrobial, pharmaceutical, medical device, and related regulated manufacturing and consumer product industries. The Senior Microbiologist performs and evaluates both custom and standardized testing that supports client needs; generates data while maintaining a high level of scientific integrity; assists in the review of test results, raw data, and Certificates of Analysis; designs and executes research and development (R&D) projects when implementing new methods or adapting current methods; maintains awareness of advances and changes in the test methodology; effectively communicates with management and others in the company to share information, offer ideas, and think creatively to effectively solve client testing problems to support registrations of new and novel antimicrobial products. In this role, you may also perform sterility and bioburden testing, environmental monitoring, and method qualifications. This position plays a key role in executing testing within a cGLP and ISO 17025 environment, maintaining data integrity, and ensuring results are scientifically sound, timely, and defensible. The Senior Microbiologist works closely with internal technical teams and external client partners and contributes directly to maintaining the high standards of quality and reliability that Element is known for. You can read a bit more about the work out Eagan lab does here: EMT Eagan Lab Page Responsibilities * Performs and leads antimicrobial efficacy testing assays including standard methods and custom methods• May perform assays including bioburden, sterility testing, microbial enumeration, organism identification, endotoxin testing, and microbial limits testing. * Conduct method development, qualification, verification, and validation activities in alignment with industry standards. * May support environmental monitoring and cleanroom qualification programs, including surface, air, and personnel monitoring. * Maintain accurate, compliant documentation within laboratory information and quality systems. * Prepare test reports, review data, and communicate results clearly and professionally to internal and external partners. * Participate in equipment maintenance, calibrations, and laboratory housekeeping to ensure safe and compliant operations. * Assist with client technical transfers and onboarding of new test methods as needed. * Ability to adapt standard laboratory techniques and tests to meet the demands of specific problems. * Ability to make complex mathematical computations, use statistical techniques in the treatment of data, and interpret and apply findings. * Work as an effective and proactive team-player; understands the importance of supporting the organization, customers, and other employees. * Ability to maintain appropriate records for all facets of job. * Able to use critical thinking, logic, and reasoning to identify the strengths and weaknesses of alternative solutions, conclusions, or approaches to problems. * Able to communicate effectively in writing as appropriate for the needs of the audience. * Able to manage work time, determine priorities, seek assistance when necessary, and complete projects within deadlines. * Identifies complex problems and reviewing related information to develop and evaluate options and implement solutions independently. * Able to plan, prioritize, coordinate, and manage work in a fast-paced environment. Able to work unsupervised, make complex level decisions independently, and solve problems effectively and creatively. * Displays high levels of customer service, responding promptly and thoroughly to the inquiries and needs of individuals both internal and external to the organization, as applicable. * Understand and maintain confidential nature of customer, organization and employee information. * Show professional knowledge, proficiency and initiative in achieving goals and meeting standards Skills / Qualifications * BS or MS in Microbiology, Biology, Medical Laboratory Science, or related discipline. * 5 years of hands-on microbiology experience in a cGLP, ISO 17025, or regulated laboratory environment. * Working knowledge of USP , , , , , , and related pharmaceutical microbiology standards. * Demonstrated experience with aseptic technique and/or cleanroom operations. * Reusable medical device testing is nice to have * Strong documentation discipline and familiarity with GxP data integrity expectations. * Ability to manage multiple projects while maintaining focus, accuracy, and compliance. * Effective written and verbal communication skills, including the ability to interpret testing procedures and prepare clear technical documentation. #LI-TK1 Company Overview Element is one of the fastest growing testing, inspection and certification businesses in the world. Globally we have more than 9,000 brilliant minds operating from 270 sites across 30 countries. Together we share an ambitious purpose to 'Make tomorrow safer than today'. When failure in use is not an option, we help customers make certain that their products, materials, processes and services are safe, compliant and fit for purpose. From early R&D, through complex regulatory approvals and into production, our global laboratory network of scientists, engineers, and technologists support customers to achieve assurance over product quality, sustainable outcomes, and market access. While we are proud of our global reach, working at Element feels like being part of a smaller company. We empower you to take charge of your career, and reward excellence and integrity with growth and development. Industries across the world depend on our care, attention to detail and the absolute accuracy of our work. The role we have to play in creating a safer world is much bigger than our organization. Diversity Statement At Element, we always take pride in putting our people first. We are an equal opportunity employer that recognizes diversity and inclusion as fundamental to our Vision of becoming "the world's most trusted testing partner". All suitably qualified candidates will receive consideration for employment on the basis of objective work related criteria and without regard for the following: age, disability, ethnic origin, gender, marital status, race, religion, responsibility of dependents, sexual orientation, or gender identity or other characteristics in accordance with the applicable governing laws or other characteristics in accordance with the applicable governing laws.

**Why Mayo Clinic** Mayo Clinic is top-ranked in more specialties than any other care provider according to U.S. News & World Report. As we work together to put the needs of the patient first, we are also dedicated to our employees, investing in competitive compensation and comprehensive benefit plans (************************************** - to take care of you and your family, now and in the future. And with continuing education and advancement opportunities at every turn, you can build a long, successful career with Mayo Clinic. **Benefits Highlights** + Medical: Multiple plan options. + Dental: Delta Dental or reimbursement account for flexible coverage. + Vision: Affordable plan with national network. + Pre-Tax Savings: HSA and FSAs for eligible expenses. + Retirement: Competitive retirement package to secure your future. **Responsibilities** Sets up and performs routine and established lab procedures in support of lab goals, grant commitments, i.e. assays, cell/tissue culture, animal studies, etc. Monitors results, reports unusual outcomes and suggests modifications. Collects, enters and summarizes data. Assists in the maintenance of lab equipment and supplies. Performs basic statistical data analysis; prepares tables/charts/graphs and assists in organizing data. Presents at research laboratory meetings and contributes to writing of manuscripts. Works under supervision and may perform some assignments independently as discussed and approved by Principal Investigator. **Qualifications** Requires bachelor's degree in biology, chemistry, other relevant science, or an associates degree with 6 years of relevant laboratory experience. Must exhibit a solid understanding of lab techniques, equipment, and safety. Must have the ability to organize and carry out laboratory techniques independently and in a team setting. Experience with basic data analysis is required. This position requires demonstrated writing skills. Experience with rodent models, tissue acquisition, histological techniques and image analysis preferred **Exemption Status** Nonexempt **Compensation Detail** Education, experience and tenure may be considered along with internal equity when job offers are extended.; $27.44-41.16/ hour **Benefits Eligible** Yes **Schedule** Full Time **Hours/Pay Period** 80 **Schedule Details** Monday-Friday, 8:00 am - 5:00 pm **Weekend Schedule** N/A **International Assignment** No **Site Description** Just as our reputation has spread beyond our Minnesota roots, so have our locations. Today, our employees are located at our three major campuses in Phoenix/Scottsdale, Arizona, Jacksonville, Florida, Rochester, Minnesota, and at Mayo Clinic Health System campuses throughout Midwestern communities, and at our international locations. Each Mayo Clinic location is a special place where our employees thrive in both their work and personal lives. Learn more about what each unique Mayo Clinic campus has to offer, and where your best fit is. (***************************************** **Equal Opportunity** All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, gender identity, sexual orientation, national origin, protected veteran status or disability status. Learn more about the "EOE is the Law" (**************************** . Mayo Clinic participates in E-Verify (******************************************************************************************** and may provide the Social Security Administration and, if necessary, the Department of Homeland Security with information from each new employee's Form I-9 to confirm work authorization. **Recruiter** Jill Squier **Equal opportunity** As an Affirmative Action and Equal Opportunity Employer Mayo Clinic is committed to creating an inclusive environment that values the diversity of its employees and does not discriminate against any employee or candidate. Women, minorities, veterans, people from the LGBTQ communities and people with disabilities are strongly encouraged to apply to join our teams. Reasonable accommodations to access job openings or to apply for a job are available.

Element has an opportunity for a Senior Microbiologist to join our Eagan, MN laboratory, which specializes in microbiological testing and analytical support for antimicrobial, pharmaceutical, medical device, and related regulated manufacturing and consumer product industries. The Senior Microbiologist performs and evaluates both custom and standardized testing that supports client needs; generates data while maintaining a high level of scientific integrity; assists in the review of test results, raw data, and Certificates of Analysis; designs and executes research and development (R&D) projects when implementing new methods or adapting current methods; maintains awareness of advances and changes in the test methodology; effectively communicates with management and others in the company to share information, offer ideas, and think creatively to effectively solve client testing problems to support registrations of new and novel antimicrobial products. In this role, you may also perform sterility and bioburden testing, environmental monitoring, and method qualifications. This position plays a key role in executing testing within a cGLP and ISO 17025 environment, maintaining data integrity, and ensuring results are scientifically sound, timely, and defensible. The Senior Microbiologist works closely with internal technical teams and external client partners and contributes directly to maintaining the high standards of quality and reliability that Element is known for. You can read a bit more about the work out Eagan lab does here: EMT Eagan Lab Page Responsibilities Performs and leads antimicrobial efficacy testing assays including standard methods and custom methods • May perform assays including bioburden, sterility testing, microbial enumeration, organism identification, endotoxin testing, and microbial limits testing. Conduct method development, qualification, verification, and validation activities in alignment with industry standards. May support environmental monitoring and cleanroom qualification programs, including surface, air, and personnel monitoring. Maintain accurate, compliant documentation within laboratory information and quality systems. Prepare test reports, review data, and communicate results clearly and professionally to internal and external partners. Participate in equipment maintenance, calibrations, and laboratory housekeeping to ensure safe and compliant operations. Assist with client technical transfers and onboarding of new test methods as needed. Ability to adapt standard laboratory techniques and tests to meet the demands of specific problems. Ability to make complex mathematical computations, use statistical techniques in the treatment of data, and interpret and apply findings. Work as an effective and proactive team-player; understands the importance of supporting the organization, customers, and other employees. Ability to maintain appropriate records for all facets of job. Able to use critical thinking, logic, and reasoning to identify the strengths and weaknesses of alternative solutions, conclusions, or approaches to problems. Able to communicate effectively in writing as appropriate for the needs of the audience. Able to manage work time, determine priorities, seek assistance when necessary, and complete projects within deadlines. Identifies complex problems and reviewing related information to develop and evaluate options and implement solutions independently. Able to plan, prioritize, coordinate, and manage work in a fast-paced environment. Able to work unsupervised, make complex level decisions independently, and solve problems effectively and creatively. Displays high levels of customer service, responding promptly and thoroughly to the inquiries and needs of individuals both internal and external to the organization, as applicable. Understand and maintain confidential nature of customer, organization and employee information. Show professional knowledge, proficiency and initiative in achieving goals and meeting standards Skills / Qualifications BS or MS in Microbiology, Biology, Medical Laboratory Science, or related discipline. 5 years of hands-on microbiology experience in a cGLP, ISO 17025, or regulated laboratory environment. Working knowledge of USP , , , , , , and related pharmaceutical microbiology standards. Demonstrated experience with aseptic technique and/or cleanroom operations. Reusable medical device testing is nice to have Strong documentation discipline and familiarity with GxP data integrity expectations. Ability to manage multiple projects while maintaining focus, accuracy, and compliance. Effective written and verbal communication skills, including the ability to interpret testing procedures and prepare clear technical documentation. #LI-TK1 Company Overview Element is one of the fastest growing testing, inspection and certification businesses in the world. Globally we have more than 9,000 brilliant minds operating from 270 sites across 30 countries. Together we share an ambitious purpose to ‘Make tomorrow safer than today'. When failure in use is not an option, we help customers make certain that their products, materials, processes and services are safe, compliant and fit for purpose. From early R&D, through complex regulatory approvals and into production, our global laboratory network of scientists, engineers, and technologists support customers to achieve assurance over product quality, sustainable outcomes, and market access. While we are proud of our global reach, working at Element feels like being part of a smaller company. We empower you to take charge of your career, and reward excellence and integrity with growth and development. Industries across the world depend on our care, attention to detail and the absolute accuracy of our work. The role we have to play in creating a safer world is much bigger than our organization. Diversity Statement At Element, we always take pride in putting our people first. We are an equal opportunity employer that recognizes diversity and inclusion as fundamental to our Vision of becoming “the world's most trusted testing partner”. All suitably qualified candidates will receive consideration for employment on the basis of objective work related criteria and without regard for the following: age, disability, ethnic origin, gender, marital status, race, religion, responsibility of dependents, sexual orientation, or gender identity or other characteristics in accordance with the applicable governing laws or other characteristics in accordance with the applicable governing laws.

Job Description Cambridge Technologies Guidelines JOB TITLE: Diagnostic Laboratory Scientist DEPARTMENT: Molecular Diagnostics DATE CREATED: 12/2/2025 A Diagnostic Laboratory Scientist will provide specialized technical support in the livestock diagnostic laboratory focused on molecular testing. This role is responsible for performing and assisting with next-generation sequencing (NGS), quantitative PCR (qPCR), bioinformatic analysis, and related molecular workflows used to detect, monitor, and characterize pathogens in livestock populations. This role also contributes to troubleshooting laboratory assays, maintaining instrumentation, implementing new methodologies, and supporting lab-wide quality assurance efforts. This role will interact with other diagnostic lab members, research team members, and other departments as needed. ACCOUNTABILITIES Reports to: Supervisor, Molecular Diagnostics Supervises: Has no supervisory responsibilities ESSENTIAL DUTIES & RESPONSIBILITIES Lead and execute advanced molecular diagnostic workflows, including nucleic acid extraction, PCR/qPCR assay development and optimization, next-generation sequencing (NGS) library preparation, and bioinformatic data analysis in accordance with company SOPs and quality standards. Work with various animal tissues and pathogens in a Biosafety level 2 environment, adhering to company safety policies. Conduct and coordinate assigned projects, experiments, or departmental activities to meet goals and timelines. Collect, maintain, and organize data in the form of a laboratory notebook, bench record, animal record, electronic project database, and/or production record Communicate data/results in the form of written or oral reports and provide suggestions for next steps. Maintain laboratory and equipment in order to meet project and regulatory requirements. Collaborate effectively with cross-functional teams, including R&D, quality assurance, production, and regulatory affairs, serving as a scientific resource and technical subject matter expert. Must be able to conduct assignments with limited supervision and accurately communicate results to the supervisor. Provide accurate and honest documentation and reporting of research data and results. Work in a safe and productive manner with the guidelines established by policy and follow good laboratory practices. Accountable for complying with the company handbook and all policies set by the company and delegated authority. Performs other duties as assigned. EDUCATION/EXPERIENCE Bachelor's degree required; advanced degree (M.S. or Ph.D.) strongly preferred in Microbiology, Molecular Biology, Veterinary Science, or a related life sciences discipline, with demonstrated experience in animal health diagnostics or veterinary biologics. Extensive hands-on experience with molecular diagnostic techniques (PCR/qPCR, sequencing, nucleic acid extraction) and with bioinformatics tools and pipelines. Working knowledge of veterinary biologics principles, including diagnostic assay development, vaccine/biologic production, quality control testing, regulatory expectations, and industry standards. Strong communication skills, including the ability to write technical reports, interpret complex data for diverse audiences, and collaborate across multidisciplinary teams. Demonstrated adherence to GMP, GLP, and general laboratory safety practices, with experience working in BSL-2 environments preferred. LANGUAGE SKILLS Ability to read and interpret documents such as safety rules, operating and maintenance instructions, and procedure manuals. Ability to write routine reports and correspondence. Ability to speak effectively before groups of customers or employees of organization. MATHEMATICAL SKILLS Ability to calculate basic laboratory mathematical calculations such as stock dilutions. REASONING ABILITY Ability to apply common sense understanding to carry out instructions furnished in written, oral, or diagram form. Ability to deal with problems involving several concrete variables in standardized situations. OTHER SKILL & ABILITIES Attention to detail. Communication skills - verbal and written. Data collection, management and analysis. Problem analysis and problem solving. Planning and organizing. Judgement. Decision-making. Customer service orientation. Teamwork. 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 frequently required to stand; walk; sit; reach with hands and arms; stoop, kneel, crouch, or crawl and talk or hear. The employee must occasionally lift and/or move up to 25-40 pounds, with occasional lifting up to 60 pounds. WORK ENVIRONMENT This position may work in a laboratory, research farm, manufacturing facility, and office setting where they conduct experiments and analyze the results. Technicians and scientists who work with biosafety level 2 organisms must follow appropriate safety procedures.

Site: The General Hospital Corporation Mass General Brigham relies on a wide range of professionals, including doctors, nurses, business people, tech experts, researchers, and systems analysts to advance our mission. As a not-for-profit, we support patient care, research, teaching, and community service, striving to provide exceptional care. We believe that high-performing teams drive groundbreaking medical discoveries and invite all applicants to join us and experience what it means to be part of Mass General Brigham. The Catherine Othieno Sempa Memorial Post Baccalaureate Scholars Program engages talented college graduates from HBCUs and Puerto Rican universities in a comprehensive and immersive two-year program in immunology research. The program is designed to strengthen the field of academic research by inviting recent college graduates to gain knowledge, expertise, and skills inside and outside the lab. Program Benefits Participants will be employed as a paid, full-time Research Technicians under the supervision and mentorship of a Ragon Institute Principal Investigator and/or designated Post-Doctoral Research Fellow. Participants will receive a competitive salary and benefits consistent with employment as a Research Technician at the Institute. In addition, participants will engage in academic and professional development activities including: * Development of an individualized training plan * Training in scientific communication * Participation in seminars and workshops * Full participation in lab meetings and Ragon affinity groups and committee * Graduate school preparation * Travel sponsorship to a national conference * Participants will also receive a $3,000 travel allowance. Job Summary Responsible for maintaining laboratory equipment, organizing and preparing samples, conducting experiments, and recording and analyzing data. Candidates who are in the process of completing their bachelor's degree have a grace period of six months from their hire date (up to 1 year if starting per diem) to provide degree equivalency verification. Does this position require Patient Care? No Essential Functions * Perform laboratory experiments following established protocols and procedures. * Prepare and handle samples, reagents, and solutions, ensuring accuracy and adherence to safety guidelines. * Operate and maintain laboratory equipment and instruments, conducting routine calibration and troubleshooting as needed. * Record experimental data accurately and maintain organized records of procedures, protocols, and results. * Compile and analyze data using appropriate statistical and analytical methods. * Assist in data interpretation and presentation, contributing to research findings and reports. Qualifications Education Bachelor's Degree Related Field of Study required Can this role accept experience in lieu of a degree? Yes Licenses and Credentials Experience Prior laboratory experience, either through academic coursework, internships, or employment 1-2 years preferred Knowledge, Skills and Abilities * Strong theoretical and practical knowledge of laboratory techniques and procedures. * Familiarity with common laboratory equipment and instruments used in research experiments. * Proficiency in data collection, analysis, and scientific software tools. * Excellent attention to detail, organizational skills, and the ability to multitask and prioritize tasks effectively. * Strong problem-solving skills and the ability to troubleshoot technical issues. * Excellent written and verbal communication skills to effectively convey experimental procedures, results, and challenges. Additional Job Details (if applicable) Program Eligibility * Have U.S. citizenship or permanent residency and be eligible to work in the US. * Completed a college or university degree (of four or more years duration) no more than one year before the start of the program. * Majored in biological sciences or biological engineering. * Attained a minimum GPA of 3.3 on a 4.0 scale. Previously participated in scientific research. * Demonstrated interest in pursuing a graduate degree in a research field (M.S., M.A, Ph.D. or M.D./Ph.D.). * This program is not designed for students primarily interested in clinical practice * This program is open to individuals from Minority Serving Institutions (MSIs), Historically Black Colleges and Universities (HBCUs) and students from the University of Puerto Rico. Important Dates: Application deadline: February 15, 2026 Start date: June-August 2025 Remote Type Onsite Work Location 600 Main Street Pay Range $19.76 - $28.44/Hourly Grade 5 At Mass General Brigham, we believe in recognizing and rewarding the unique value each team member brings to our organization. Our approach to determining base pay is comprehensive, and any offer extended will take into account your skills, relevant experience if applicable, education, certifications and other essential factors. The base pay information provided offers an estimate based on the minimum job qualifications; however, it does not encompass all elements contributing to your total compensation package. In addition to competitive base pay, we offer comprehensive benefits, career advancement opportunities, differentials, premiums and bonuses as applicable and recognition programs designed to celebrate your contributions and support your professional growth. We invite you to apply, and our Talent Acquisition team will provide an overview of your potential compensation and benefits package. EEO Statement: The General Hospital Corporation is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religious creed, national origin, sex, age, gender identity, disability, sexual orientation, military service, genetic information, and/or other status protected under law. We will ensure that all individuals with a disability are provided a reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. To ensure reasonable accommodation for individuals protected by Section 503 of the Rehabilitation Act of 1973, the Vietnam Veteran's Readjustment Act of 1974, and Title I of the Americans with Disabilities Act of 1990, applicants who require accommodation in the job application process may contact Human Resources at **************. Mass General Brigham Competency Framework At Mass General Brigham, our competency framework defines what effective leadership "looks like" by specifying which behaviors are most critical for successful performance at each job level. The framework is comprised of ten competencies (half People-Focused, half Performance-Focused) and are defined by observable and measurable skills and behaviors that contribute to workplace effectiveness and career success. These competencies are used to evaluate performance, make hiring decisions, identify development needs, mobilize employees across our system, and establish a strong talent pipeline.

Sets up and performs routine and established lab procedures in support of lab goals, grant commitments, i.e. assays, cell/tissue culture, animal studies, etc. Monitors results, reports unusual outcomes and suggests modifications. Collects, enters and summarizes data. Assists in the maintenance of lab equipment and supplies. Performs basic statistical data analysis; prepares tables/charts/graphs and assists in organizing data. Presents at research laboratory meetings and contributes to writing of manuscripts. Works under supervision and may perform some assignments independently as discussed and approved by Principal Investigator. Requires bachelor's degree in biology, chemistry, other relevant science, or an associates degree with 6 years of relevant laboratory experience. Must exhibit a solid understanding of lab techniques, equipment, and safety. Must have the ability to organize and carry out laboratory techniques independently and in a team setting. Experience with basic data analysis is required. This position requires demonstrated writing skills. Experience with rodent models, tissue acquisition, histological techniques and image analysis preferred

NAMSA pioneered the industry and was the first independent company in the world to focus solely on medical device materials for safety. NAMSA started testing medical devices before the U.S. Food and Drug Administration started regulating such products in 1976. We are shaping the industry. NAMSA has been a key contributor to the development of the test methods that govern our industry. We have become the industry's premier provider. We provide support for clients during every step of the product development lifecycle and beyond. Come and work for an organization with the: Vision to inspire innovative MedTech solutions that advance global healthcare, improve patient lives and accelerate Client success and the Mission to deliver best-in-class global MedTech development solutions through our people, expertise and technology by adhering to our core Values: Act with integrity in everything we do. Provide best-in-class customer experiences. Develop superior talent and deliver expertise. Respond with agility and provide timely results. Embrace collaboration, diverse perspectives and ideas. Job Description: • Dispenses medications as prescribed by veterinarian and/or protocol specifications. • Performs and documents a variety of activities, including but not limited to, routine clinical observations, charting of physiological data and animal health status, taking study-required animal weights, documentation of maintenance medicine administration, etc. • Administers start-up medications, monitors the fasting of animals and clinical observations. • Monitors animals during their critical recovery phase on the days following surgery, including performing TPRs (temp, pulse, and respiration), auscultation of the heart and lungs, assessing pain of animals at incision sites, changing wound dressings and administering medications. • Performs intravenous blood draws. • Performs preventive health maintenance such as administering maintenance medications, administering anthelmintics and vaccinations, ointment applications, hoof and nail trims including sedation as needed, bathing, and ear cleaning. • Performs all aspects of veterinary care and general husbandry procedures according to established procedures, guidelines and study protocols that meet the acceptable criteria of the veterinarian. • Communicates with veterinary staff, supervisor and study directors regarding living conditions and medical status of animals. • Assists with training newer large animal research technicians. • Assists with other duties as assigned. Qualifications & Technical Competencies: • Associate of Science in Veterinary Technology or 4 years of related experience required. • Bachelor's degree in scientific discipline is preferred. • Certified Veterinary Technician (CVT) or ALAT certification is preferred. Working Conditions: • While performing the duties of this job, the employee is regularly exposed to, and must handle and come in contact with, a variety of large and small livestock, domestic and laboratory animals, as well as their blood and body fluids. The employee is frequently exposed to sharps, wet conditions (non-weather) and toxic or caustic chemicals. The employee is occasionally exposed to fluoroscopy, required to work with in a Bio-Safety-Level 2 (BSL2) environment, and on rare occasions is exposed to faxitron x-ray imaging. The employee may occasionally be exposed to gasses such as CO2 and isoflurane, and zoonotic diseases. • The noise level in the work environment is usually moderate and frequently loud. Hearing protection is required in designated areas and when performing specific tasks. • While performing the duties of this job, the employee is regularly required to stand, walk, use hands, and talk or hear. The employee is frequently required to reach with hands and arms, grasp, hold and manipulate equipment with hands, stoop, crouch, and kneel. The employee is occasionally required to sit, climb, balance, or crawl. The employee must frequently lift and/or move up to 50 pounds, and occasionally lift and/or move up to 75 pounds with assistance. The employee may be required to view computer monitors and stand for extended periods of time. • Specific vision abilities required by this job include close vision, the ability to see a full range of colors, the ability to adjust focus, exceptional spatial acuity and visual-kinesthetic coordination. Pay Range Minimum: $14.81 Pay Range Target: $23.00 Pay Frequency: Hourly Please Note: Individual base pay depends on various factors, in addition to primary work location, such as complexity and responsibility of role, job duties/requirements, and relevant experience and skills.

Job Description Come join CCRM Fertility, a global pioneer in fertility treatment, research, science, specializing in IVF, fertility testing, egg freezing, preimplantation genetic testing, third party reproduction and egg donation. As a member of CCRM Fertility's diverse team of professionals, you will be a part of helping families grow and changing lives. We take pride in providing our employees with meaningful employment, a supportive culture, and a well-balanced personal & work life alignment. For more information, visit *************** Location Address: Department: Embryology (IVF) Lab Work Schedule: Monday - Friday and weekends as needed What We Offer Our Team Members: Generous Paid time-off (PTO) and paid holidays Medical, Dental, and Vision Insurance Health benefits eligible the first day of the month following your start date. 401(k) Plan with Company Match (first of the month following 2 months of service) Basic & Supplement Life Insurance Employee Assistance Program (EAP) Short-Term Disability Flexible spending including Dependent Care and Commuter benefits. Health Savings Account CCRM Paid Family Medical Leave (eligible after 1 year) Supplemental Options (Critical Illness, Hospital Indemnity, Accident) Bonus Potential 401(k) Plan with Company Match (first of the month following 2 months of service) Professional Development, Job Training The Junior Embryologist plays a crucial role in the field of reproductive medicine, focusing on the development and management of embryos in a clinical setting. This position involves working closely with senior embryologists and medical professionals to ensure the highest standards of care and success rates in assisted reproductive technologies. The primary end result of this role is to contribute to the successful conception and birth of healthy babies, providing hope and support to families. The Junior Embryologist will be responsible for performing laboratory procedures, maintaining equipment, and adhering to strict protocols to ensure the safety and quality of embryonic development. Ultimately, this role is vital in advancing reproductive health and helping individuals achieve their family-building goals. Minimum Qualifications: Bachelor's degree in Biology, Biochemistry, or a related field. Experience in a laboratory setting, preferably in a clinical or reproductive health environment. Strong attention to detail and ability to follow strict protocols and procedures. Preferred Qualifications: Master's degree in Reproductive Biology or a related field. Familiarity with assisted reproductive technologies and embryology laboratory techniques. Certification from a recognized professional organization in embryology or reproductive technology. Responsibilities: Assist in the preparation and analysis of gametes and embryos for in vitro fertilization (IVF) procedures. Perform routine laboratory tasks such as media preparation, cryopreservation, and embryo culture. Maintain accurate records of laboratory procedures and patient information in compliance with regulatory standards. Collaborate with senior embryologists and medical staff to optimize laboratory protocols and improve patient outcomes. Participate in quality control measures and contribute to the maintenance of a clean and organized laboratory environment. Skills: The required skills for this position include strong analytical abilities and attention to detail, which are essential for accurately performing laboratory procedures and analyzing results. Effective communication skills are also important, as the Junior Embryologist will need to collaborate with a diverse team of medical professionals and provide updates on patient progress. Time management skills are crucial for balancing multiple tasks and ensuring that all laboratory processes are completed efficiently. Preferred skills, such as familiarity with advanced laboratory techniques, will enhance the candidate's ability to contribute to innovative practices within the team. Overall, both required and preferred skills will be utilized daily to ensure the highest quality of care for patients undergoing fertility treatments. CCRM's Compensation: The salary range represents the national average compensation for this position. The base salary offered will vary based on location, experience, skills, and knowledge. The pay range does not reflect the total compensation package. Our rewards may include an annual bonus, flexible work arrangements, and many other region-specific benefits. Pre-Employment Requirements: All offers of employment are conditional upon the successful completion of the CCRM Fertility onboarding process, including verification of eligibility and authorization to work in the United States. This employer participates in the E-Verify Program in order to verify the identity and work authorization of all newly hired employees. Equal Employment/Anti-Discrimination: We are an equal-opportunity employer. In all aspects of employment, including the decision to hire, promote, discipline, or discharge, the choice will be based on merit, competence, performance, and business needs. We do not discriminate on the basis of race, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical condition, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, or any other status protected under federal, state, or local law.

The Technician will perform raw material validation testing to support global qualification efforts. This role involves executing test protocols, documenting results, and ensuring compliance with performance standards. The Technician collaborates with lab management, project teams, and regional R&D to streamline material approvals. Primary Responsibilities: -Conduct raw material validation testing using approved methods and equipment -Record and analyze results in the Electronic Lab Notebook (ELN) -Support onboarding of new materials and alternatives -Maintain lab equipment, substrates, and supplies for testing readiness -Collaborate with regional teams on substrate-specific performance needs -Participate in training and continuous improvement initiatives -Prepare data for dashboard reporting and KPI tracking -Ensure compliance with safety, documentation, and quality standards Qualifications + High school diploma or equivalent + 2+ years of laboratory experience + Proficiency in documentation and data entry + Ability to work independently and in teams + Strong communication and problem-solving skills Preferred Requirements + Coursework in science or related fields + Familiarity with adhesives and performance testing + Knowledge of lab safety and quality protocols Job Type & Location This is a Contract to Hire position based out of Saint Paul, MN. Pay and Benefits The pay range for this position is $23.00 - $26.00/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: - Medical, dental & vision - Critical Illness, Accident, and Hospital - 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available - Life Insurance (Voluntary Life & AD&D for the employee and dependents) - Short and long-term disability - Health Spending Account (HSA) - Transportation benefits - Employee Assistance Program - Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in Saint Paul,MN. Application Deadline This position is anticipated to close on Dec 17, 2025. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com (%20actalentaccommodation@actalentservices.com) for other accommodation options.

DEPARTMENT: Laboratory EXEMPTION STATUS: Non-exempt / Hourly Shafer, MN DATE PREPARED: December 2025 STATUS Full - time MONDAY - FRIDAY Duties include receipt of client samples, unpacking coolers of containers and logging samples into a Laboratory Information Management System (LIMS). Additional responsibilities include working in the microbiology laboratory to assist with basic water sample testing for coliform bacteria. DUTIES & RESPONSIBILITIES Ability to follow standard operating procedures, computer data entry with attention to detail and ability to multitask. Must be able to lift 50 pounds. Environmental sample receipt from clients and work order submittal into Laboratory LIMS system; Evaluation and distribution of daily laboratory work orders to analysts. Distribution of sampling supplies to clientele and field personnel, Maintain sample work order productivity by evaluating receiving samples; the samples are selected and grouped by parameter to expedite analysis and minimize turn-around-time. Rush service samples, as well as those with short holding times, are prioritized and analyzed accordingly. Ensure sample compliance with EPA regulated sample collection, storage, and transportation guidelines; by providing accurate sampling guidance and education to clients; consulting with clients to ensure adherence with field and laboratory quality assurance measures; and providing proper guidance of standard operating procedure and EPA methodologies as applicable to sample receipt operations, Conflict resolution and troubleshooting by consulting with clientele, assigned project manager, and/or Laboratory Director, Maintain confidential sample and client information in the Laboratory Information Management System (LIMS), Provide billing with work orders, as applicable, Maintain laboratory sample collection supply inventory by checking stock to determine inventory levels and anticipating supply needs. Maintain professional and technical knowledge by reviewing current EPA and RMB standard operating procedures, requirements, and guidelines, reviewing internal laboratory quality control and assurance procedures, • Maintain safety of the workplace and coordinate with Facilities Manager and Laboratory Director to maintain compliance with laboratory and OSHA requirements, EDUCATION & EXPERIENCE The type of formal education and type/amount of experience that would typically be needed to successfully perform in the position. Experience in Laboratory setting is welcomed. KNOWLEDGE, SKILLS & ABILITIES Skills - Measurable or observable behavior while performing a cognitive or manual activity, such as skill in word processing. Ability - Natural (perhaps innate) talents or gained capabilities, such as ability to follow procedures. Quality control and quality assurance understanding Safety conscience Current technology and trends Express ideas clearly, concisely, and effectively orally and in writing Exercise appropriate judgment in answering questions and releasing information; analyze and project consequences of decision and/or recommendations. Communicate effectively with a variety of individuals representing diverse cultures and backgrounds and function calmly in situations which require high degree of sensitivity, tack, and diplomacy. An ability to plan, organize and prioritize work. WORKING CONDITIONS The environment in which the position functions and the frequency of exposure, such as frequent exposure; Exposure to Sulfuric Acid, Nitric Acid, Potassium Iodide and Starch solution. Employees must follow safety measures. Frequent: walking, standing, bending, and twisting of neck, bending, and twisting of waist, lifting and carrying objects weighing up to 15 pounds, lifting of up to 50 lbs. Occasional: sitting, repetitive use of hands to operate instruments, computers, printers, copiers. EEO Statement RMB Environmental Laboratory is an Equal Opportunity Employer and will not discriminate against any applicant for employment on the basis of race, age, religion, sex, veterans, individuals with disabilities, sexual orientation, or gender identity. Note: Job Descriptions are not exhaustive lists of all skills, responsibilities, or efforts associated with a job. They reflect principal job elements essential for performing the job and evaluating performance. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions of the position.

Element has an opportunity for a Senior Microbiologist to join our Eagan, MN laboratory, which specializes in microbiological testing and analytical support for antimicrobial, pharmaceutical, medical device, and related regulated manufacturing and consumer product industries. The Senior Microbiologist performs and evaluates both custom and standardized testing that supports client needs; generates data while maintaining a high level of scientific integrity; assists in the review of test results, raw data, and Certificates of Analysis; designs and executes research and development (R&D) projects when implementing new methods or adapting current methods; maintains awareness of advances and changes in the test methodology; effectively communicates with management and others in the company to share information, offer ideas, and think creatively to effectively solve client testing problems to support registrations of new and novel antimicrobial products. In this role, you may also perform sterility and bioburden testing, environmental monitoring, and method qualifications. This position plays a key role in executing testing within a cGLP and ISO 17025 environment, maintaining data integrity, and ensuring results are scientifically sound, timely, and defensible. The Senior Microbiologist works closely with internal technical teams and external client partners and contributes directly to maintaining the high standards of quality and reliability that Element is known for. You can read a bit more about the work out Eagan lab does here: EMT Eagan Lab Page Responsibilities Performs and leads antimicrobial efficacy testing assays including standard methods and custom methods • May perform assays including bioburden, sterility testing, microbial enumeration, organism identification, endotoxin testing, and microbial limits testing. Conduct method development, qualification, verification, and validation activities in alignment with industry standards. May support environmental monitoring and cleanroom qualification programs, including surface, air, and personnel monitoring. Maintain accurate, compliant documentation within laboratory information and quality systems. Prepare test reports, review data, and communicate results clearly and professionally to internal and external partners. Participate in equipment maintenance, calibrations, and laboratory housekeeping to ensure safe and compliant operations. Assist with client technical transfers and onboarding of new test methods as needed. Ability to adapt standard laboratory techniques and tests to meet the demands of specific problems. Ability to make complex mathematical computations, use statistical techniques in the treatment of data, and interpret and apply findings. Work as an effective and proactive team-player; understands the importance of supporting the organization, customers, and other employees. Ability to maintain appropriate records for all facets of job. Able to use critical thinking, logic, and reasoning to identify the strengths and weaknesses of alternative solutions, conclusions, or approaches to problems. Able to communicate effectively in writing as appropriate for the needs of the audience. Able to manage work time, determine priorities, seek assistance when necessary, and complete projects within deadlines. Identifies complex problems and reviewing related information to develop and evaluate options and implement solutions independently. Able to plan, prioritize, coordinate, and manage work in a fast-paced environment. Able to work unsupervised, make complex level decisions independently, and solve problems effectively and creatively. Displays high levels of customer service, responding promptly and thoroughly to the inquiries and needs of individuals both internal and external to the organization, as applicable. Understand and maintain confidential nature of customer, organization and employee information. Show professional knowledge, proficiency and initiative in achieving goals and meeting standards Skills / Qualifications BS or MS in Microbiology, Biology, Medical Laboratory Science, or related discipline. 5 years of hands-on microbiology experience in a cGLP, ISO 17025, or regulated laboratory environment. Working knowledge of USP , , , , , , and related pharmaceutical microbiology standards. Demonstrated experience with aseptic technique and/or cleanroom operations. Reusable medical device testing is nice to have Strong documentation discipline and familiarity with GxP data integrity expectations. Ability to manage multiple projects while maintaining focus, accuracy, and compliance. Effective written and verbal communication skills, including the ability to interpret testing procedures and prepare clear technical documentation. #LI-TK1 Diversity Statement At Element, we always take pride in putting our people first. We are an equal opportunity employer that recognizes diversity and inclusion as fundamental to our Vision of becoming “the world's most trusted testing partner”. All suitably qualified candidates will receive consideration for employment on the basis of objective work related criteria and without regard for the following: age, disability, ethnic origin, gender, marital status, race, religion, responsibility of dependents, sexual orientation, or gender identity or other characteristics in accordance with the applicable governing laws or other characteristics in accordance with the applicable governing laws.

Cambridge Technologies Guidelines JOB TITLE: Diagnostic Laboratory Scientist DEPARTMENT: Molecular Diagnostics DATE CREATED: 12/2/2025 A Diagnostic Laboratory Scientist will provide specialized technical support in the livestock diagnostic laboratory focused on molecular testing. This role is responsible for performing and assisting with next-generation sequencing (NGS), quantitative PCR (qPCR), bioinformatic analysis, and related molecular workflows used to detect, monitor, and characterize pathogens in livestock populations. This role also contributes to troubleshooting laboratory assays, maintaining instrumentation, implementing new methodologies, and supporting lab-wide quality assurance efforts. This role will interact with other diagnostic lab members, research team members, and other departments as needed. ACCOUNTABILITIES Reports to: Supervisor, Molecular Diagnostics Supervises: Has no supervisory responsibilities ESSENTIAL DUTIES & RESPONSIBILITIES * Lead and execute advanced molecular diagnostic workflows, including nucleic acid extraction, PCR/qPCR assay development and optimization, next-generation sequencing (NGS) library preparation, and bioinformatic data analysis in accordance with company SOPs and quality standards. * Work with various animal tissues and pathogens in a Biosafety level 2 environment, adhering to company safety policies. * Conduct and coordinate assigned projects, experiments, or departmental activities to meet goals and timelines. * Collect, maintain, and organize data in the form of a laboratory notebook, bench record, animal record, electronic project database, and/or production record * Communicate data/results in the form of written or oral reports and provide suggestions for next steps. * Maintain laboratory and equipment in order to meet project and regulatory requirements. * Collaborate effectively with cross-functional teams, including R&D, quality assurance, production, and regulatory affairs, serving as a scientific resource and technical subject matter expert. * Must be able to conduct assignments with limited supervision and accurately communicate results to the supervisor. * Provide accurate and honest documentation and reporting of research data and results. * Work in a safe and productive manner with the guidelines established by policy and follow good laboratory practices. * Accountable for complying with the company handbook and all policies set by the company and delegated authority. * Performs other duties as assigned. EDUCATION/EXPERIENCE * Bachelor's degree required; advanced degree (M.S. or Ph.D.) strongly preferred in Microbiology, Molecular Biology, Veterinary Science, or a related life sciences discipline, with demonstrated experience in animal health diagnostics or veterinary biologics. * Extensive hands-on experience with molecular diagnostic techniques (PCR/qPCR, sequencing, nucleic acid extraction) and with bioinformatics tools and pipelines. * Working knowledge of veterinary biologics principles, including diagnostic assay development, vaccine/biologic production, quality control testing, regulatory expectations, and industry standards. * Strong communication skills, including the ability to write technical reports, interpret complex data for diverse audiences, and collaborate across multidisciplinary teams. * Demonstrated adherence to GMP, GLP, and general laboratory safety practices, with experience working in BSL-2 environments preferred. LANGUAGE SKILLS Ability to read and interpret documents such as safety rules, operating and maintenance instructions, and procedure manuals. Ability to write routine reports and correspondence. Ability to speak effectively before groups of customers or employees of organization. MATHEMATICAL SKILLS Ability to calculate basic laboratory mathematical calculations such as stock dilutions. REASONING ABILITY Ability to apply common sense understanding to carry out instructions furnished in written, oral, or diagram form. Ability to deal with problems involving several concrete variables in standardized situations. OTHER SKILL & ABILITIES Attention to detail. Communication skills - verbal and written. Data collection, management and analysis. Problem analysis and problem solving. Planning and organizing. Judgement. Decision-making. Customer service orientation. Teamwork. 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 frequently required to stand; walk; sit; reach with hands and arms; stoop, kneel, crouch, or crawl and talk or hear. The employee must occasionally lift and/or move up to 25-40 pounds, with occasional lifting up to 60 pounds. WORK ENVIRONMENT This position may work in a laboratory, research farm, manufacturing facility, and office setting where they conduct experiments and analyze the results. Technicians and scientists who work with biosafety level 2 organisms must follow appropriate safety procedures.

Sets up and performs routine and established lab procedures in support of lab goals, grant commitments, i.e. assays, cell/tissue culture, animal studies, etc. Monitors results, reports unusual outcomes and suggests modifications. Collects, enters and summarizes data. Assists in the maintenance of lab equipment and supplies. Performs basic statistical data analysis; prepares tables/charts/graphs and assists in organizing data. Presents at research laboratory meetings and contributes to writing of manuscripts. Works under supervision and may perform some assignments independently as discussed and approved by Principal Investigator. Requires bachelor's degree in biology, chemistry, other relevant science, or an associates degree with 6 years of relevant laboratory experience. Must exhibit a solid understanding of lab techniques, equipment, and safety. Must have the ability to organize and carry out laboratory techniques independently and in a team setting. Experience with basic data analysis is required. This position requires demonstrated writing skills. Experience with rodent models, tissue acquisition, histological techniques and image analysis preferred

Vantive is a vital organ therapy company on a mission to extend lives and expand possibilities for patients and care teams everywhere. For 70 years, our team has driven meaningful innovations in kidney care. As we build on our legacy, we are deepening our commitment to elevating the dialysis experience through digital solutions and advanced services, while looking beyond kidney care and investing in transforming vital organ therapies. Greater flexibility and efficiency in therapy administration for care teams, and longer, fuller lives for patients- that is what Vantive aspires to deliver. We believe Vantive will not only build our leadership in the kidney care space, it will also offer meaningful work to those who join us. At Vantive, you will become part of a community of people who are focused, courageous and don't settle for the mediocre. Each of us is driven to help improve patients' lives worldwide. Join us in advancing our mission to extend lives and expand possibilities. Your Role R&D Sterility Assurance has an exciting Microbiology Laboratory Technician III opportunity to start your career. You will work with a growing, high energy, knowledgeable team and work on R&D projects including innovation and new product development activities. This could also be an opportunity to develop your career through engagement with other functions such as Manufacturing, Quality and other R&D locations. The Oakdale Laboratory Technician III will report to the Oakdale, MN Microbiology Lab Manager and be responsible for performing daily functions of the microbiology lab to support testing. This includes, but not limited to, supporting testing and following instructions of senior microbiologists, maintaining lab equipment, making media and facilitating testing as directed by the manager. What you'll be doing Assist experienced Microbiologists in the design, development, and building of test protocols and monitoring strategies, appropriate with experience level. Make and record observations, perform simple calculations. Collect and prepare technical data for evaluation. Proficient with data entry and computer applications. Experience in a Micro Lab either in medical devices , pharmaceutical or other industrial setting, and background in aseptic techniques preferred. Perform routine microbiology processes and procedures using aseptic techniques and Good Laboratory Practices (GLP). Obtains and tests samples for bioburden testing. Performs monthly environmental settle plates. Performs microbial testing according to established test methods. Performs gram stain and LPCB staining. Completes testing projects from beginning to end. Maintains supply arrival, COA, labeling and inventory. Responsible for shipping samples for testing at a contract laboratory. Accountable for shipping equipment for maintenance and in-house equipment calibrations and those done by outside contractors. Maintains laboratory cleanliness, housekeeping chores and cleaning glassware. Accurately label samples. Follow guidelines when recording data. Accurately calculate, interpret, and report results. Accurately maintain laboratory data and logs using electronic lab notebook. Demonstrate flexibility, i.e. willingly take on new tasks. Collaborate in cross-functional teams. Follow designated work schedule. Accept and act upon supervisory directions. What you'll bring Associate degree in microbiology or similar field preferred or combination of education and/or work experience. Basic knowledge of microbiology and laboratory concepts and techniques. Basic knowledge of computer applications. Vantive is committed to supporting the needs for flexibility in the workplace. We do so through our flexible workplace policy which includes a minimum of 3 days a week onsite. This policy provides the benefits of connecting and collaborating in-person in support of our Mission. We understand compensation is an important factor as you consider the next step in your career. At Vantive, we are committed to equitable pay for all employees, and we strive to be more transparent with our pay practices. The estimated base salary for this position is $68,000-102,000 annually. The estimated range is meant to reflect an anticipated salary range for the position. We may pay more or less than of the anticipated range based upon market data and other factors, all of which are subject to change. Individual pay is based on upon location, skills and expertise, experience, and other relevant factors. This position may also be eligible for discretionary bonuses, and/or long-term incentive. For questions about this, our pay philosophy, and available benefits, please speak to the recruiter if you decide to apply and are selected for an interview. US Benefits at Vantive This is where your well-being matters. Vantive offers comprehensive compensation and benefits packages for eligible roles. Our health and well-being benefits include medical, dental and vision coverage that start on day one, as well as insurance coverage for basic life, accident, short-term and long-term disability, and business travel accident insurance. Financial and retirement benefits include the Aon Pooled Employer Plan (“Aon PEP”), Vantive's 401(k) retirement savings plan, to help you prepare for your future. The Aon PEP is designed to help improve retirement outcomes by providing retirement resources more efficiently. The plan offers a robust set of investment options, financial education, and a suite of resources to support your retirement goals. We also offer Flexible Spending Accounts, educational assistance programs, and time-off benefits such as paid holidays, paid time off ranging from 20 to 35 days based on length of service, family and medical leaves of absence, and paid parental leave. Additional benefits include commuting benefits, the Employee Discount Program, the Employee Assistance Program (EAP), and childcare benefits. Join us and enjoy the competitive compensation and benefits we offer to our employees. For additional information regarding Vantive's US Benefits, please speak with your recruiter or visit our Benefits site: Benefits | Vantive Equal Employment Opportunity Vantive is an equal opportunity employer. Vantive evaluates qualified applicants without regard to race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, protected veteran status, disability/handicap status or any other legally protected characteristic. Know Your Rights: Workplace Discrimination is Illegal Reasonable Accommodation Vantive is committed to working with and providing reasonable accommodations to individuals with disabilities globally. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please click on the link here and let us know the nature of your request along with your contact information. Form Link Recruitment Fraud Notice Vantive has discovered incidents of employment scams, where fraudulent parties pose as Vantive employees, recruiters, or other agents, and engage with online job seekers in an attempt to steal personal and/or financial information. To learn how you can protect yourself, review our Recruitment Fraud Notice.

Join our dynamic team in the Microbiology lab as a Support Lab Technician/Lab Assistant where you'll perform fast-paced and repetitive laboratory support functions. This role is focused on support tasks rather than performing analysis, making it ideal for individuals who thrive in a structured and team-oriented environment. Responsibilities * Process and dispose of hazardous waste, comprising 25-33% of the role, approximately 2 hours a day. * Sterilize and wash containers and glassware to maintain laboratory cleanliness. * Organize and receive all lab supplies, stock shelves, and manage inventory. * Register samples into the Laboratory Information Management System (LIMS). * Participate in sample preparation training to develop further skills. Essential Skills * Proficiency in aseptic technique and sample preparation. * Strong data documentation skills. * Positive attitude and willingness to learn, verified by references. * Standard Operating Procedures (SOP) Additional Skills & Qualifications * A bachelor's degree is NOT required but beneficial for those comfortable in a longer-term lab support role. * Flexibility and adaptability in a laboratory setting. Work Environment The role is 100% laboratory-based, operating within an outsourced microbiology testing lab environment certified by ISO standards. This controlled setting aims to prevent contamination and involves wearing full smocks, lab glasses, lab shoes, jeans, and lab coats, akin to a low-level clean room. The schedule is Monday to Friday, from 10:30 am to 7 pm, with some flexibility on start and end times. Job Type & Location This is a Contract to Hire position based out of Mounds View, MN. Pay and Benefits The pay range for this position is $17.00 - $17.00/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life & AD&D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in Mounds View,MN. Application Deadline This position is anticipated to close on Dec 25, 2025. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.