Microbiologist jobs in Colorado

Kelly Science & Clinical is seeking a Research Associate - Process Analytics for a contract position at a cutting-edge Client in Louisville, CO. If you're passionate about bringing the latest scientific discoveries to life and are ready to take the next step in your career, trust The Experts at Hiring Experts. Pay: $61,200 - $75,600 Schedule: Full-time Onsite Mon-Fri Overview Client is a game-changing biotech start-up focused on transforming the treatment of cancer with a novel integrated immunotherapy platform. Their vision is to develop off-the-shelf therapies capable of treating any tumor, any time. This position plays a critical role in advancing Client's pipeline and analytical development capabilities. The Research Associate will support characterization of Lentiviral Vector (LVV) and work closely with other functions to test LVV samples. Responsibilities: Assist with method design, execution, and analysis to support development of gene therapy products Perform routine impurity and characterization testing (e.g., ELISA, qPCR, dd PCR, flow cytometry) to support process development Maintain clear records of experimental work using an electronic notebook system that adheres to company guidelines Manage sample submissions in Benchling for assigned methods and ensure timely data turnaround Exemplify company core values and adhere to policies to ensure safety and quality of gene therapy products and facility Qualifications: BS in Biology, Biochemistry, or related discipline with no previous working experience OR Associate's Degree and 2 years of hands-on laboratory experience (equivalent combinations of education and experience considered) Hands-on experience with one or more of the following techniques: dd PCR, qPCR, ELISA, and flow cytometry required Preferred Qualifications: Excellent communication skills and ability to work collaboratively in a multidisciplinary team Experience with basic data analysis is a plus Self-motivated, organized, and clear documentation skills Ability to work in a fast-paced environment, meet deadlines, and prioritize multiple projects Physical Requirements: 100% compliance with PPE requirements in laboratory environments Ability to perform physical tasks including standing, walking, bending, kneeling, and occasionally lifting up to 50 lbs Regular on-site presence required for analytical development and execution What happens next: Once you apply, you'll proceed to next steps if your skills and experience look like a good fit. But don't worry - even if this position doesn't work out, you're still in our network. That means our team of expert Science & Clinical recruiters will have access to your profile, making your opportunities limitless.

Pinnacle Real Estate Advisors, a local, high growth, dynamic, and energetic commercial real estate firm, seeks a full-time Database Associate to implement and manage the company's commercial database. This role is ideal for individuals looking to launch a career in commercial real estate brokerage, transaction management, or related roles. The Database Associate position functions as a training ground within the firm-offering exposure to all product types, opportunities to meet potential teams, and hands-on learning with our proprietary shared database and industry-leading software. It is a stepping-stone to advancement, with many prior associates transitioning into brokerage or transaction management roles. Must be hardworking, trustworthy, and organized, with a strong ability to multi-task. A can-do attitude is a must, along with the ability to learn quickly and adapt to a demanding work environment. This is a great opportunity to gain an understanding of the inner workings of a commercial real estate firm. The ideal candidate will fulfill this position for a minimum of one year prior to seeking advancement within the company, typically transitioning to an Associate Advisor brokerage role. The Database Associate will be responsible for providing exemplary support, gaining industry knowledge, and positioning themselves for unlimited growth potential. Duties include but not limited to: Assist all commercial brokers by building, maintaining, and managing Real Estate Assistant (REA), a contact management program combined with eight relational databases designed specifically to track commercial real estate data Opportunity to learn and utilize CoStar and other pertinent software programs, including CLEAR, Real Quest and LoopNet. Complete market research as necessary by collecting and analyzing property data. Assist with day-to-day operations of the company, including, but not limited to, creating and binding tour packages, preparing mailers, updating data book, taking property photos, and various administrative duties upon request. Ability to network with seasoned brokers in all commercial product types. Perform other miscellaneous administrative and clerical duties as needed. Position requirements: Previous experience in the commercial real estate industry preferred. Well-versed in Microsoft Office applications (PowerPoint, EXCEL, Word and Outlook). Knowledge of or ability to quickly learn technology platforms to support various forms. Excellent verbal and written communication skills are necessary. Ability to see the “big picture” and work hard. Resourceful, well organized, highly dependable, efficient and detail oriented. Position benefits: Competitive base salary starting at $19/Hour. Salary offers will be based on the candidate's qualifications. Potential for longevity bonuses. An all-purpose PTO plan. Insurance benefits including medical coverage for employees (Pinnacle pays up to 60% coverage costs for employee, and 50% for dependents) with dental and vision offerings. 401(k) plan with employer contributions. To apply please email your resume to EAnderson@pinnacle REA.com Please list "Database Associate" in the subject line. Pinnacle Real Estate Advisors, 1 Broadway, Suite 300A, Denver, CO 80203 No phone calls please.

Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 1996. Our mission centers on delivering only the best quality talent, the first time and every time. We provide quality resources in four specialty areas: Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing. Job Description Job title: Microbiologist Location: Boulder, CO Duration: 12+ months (Possibility of extension) JOB ROLE The Microbiologist I position coordinates microbiological testing on Raw Material, Finished Products and QA samples - such as Sterility Testing, Bacterial Endotoxin testing, Particulate Matter testing, Bioburden test, Antibiotic assays, Microbial Limits test, Preservative Effectiveness test, Container Closure Integrity test and Bacterial Retention tests. Support validation functions. Performs enumeration of Biological Indicators. Maintains user logs and BI history data. Helps to maintain environmental monitoring results and and identifies environmental isolates and challenge areas. Performs evaluation of resistance microorganisms or spikes in bioburden. The position will support the performance and documentation for recertification of clean rooms and plant systems. Follows the company Safety, Health, and Environmental policies and procedures. ESSENTIAL FUNCTIONS: Responsible for specific scientific testing and provides back-up on other key test areas. Performs testing to meet USP, ISO, EN, and ASTM standards for product release and QC testing. Implement test procedures for updates and changes. Accountable for specific test data and can train on specific lab tests. Perform laboratory duties to support department objectives. Supports the Quality Assurance Program for external audits (FDA, ISO 9000) Responsible for compliance with EHS goals for this position Responsible for compliance with Quality goals for this position Responsible for compliance the trainings assigned on line or interactive. Responsible to know the impact about the inadequate performance of his\her work in the products defects. When applicable sterilization batch review and release DEPARTMENT SPECIFIC/NON-ESSENTIAL FUNCTIONS: Other duties as assigned with or without accommodation. All employees are expected to pay attention to and work in support of a safe and healthy work environment. This includes following the established rules, policies and practices of environmental, health and safety with specific attention to the Client Cardinal Rules. Performs other duties and responsibilities, as required. MINIMUM REQUIREMENTS: Education required/ Preferred: • BS/AS in Microbiology or equivalent scientific field Experience: • 1-3 years of experience in a Microbiology Lab with at least 1 year in a Medical Device environment Preferred Skills/Qualifications: Skills/Competencies: Customer Focus Ethics & Values Managing an Measuring Work Action Oriented Problem Solving Decision Quality Informing Other Skills: General knowledge of cGMP's/ISO 13485: 2003 Validations Computer Software Knowledge (Word, Excel) Additional Information We do have referral bonus of $500 per candidate, if you refer any of your friends or colleague who are looking out for the same job. Thanks & Regards, Seema Chawhan Clinical Recruiter Integrated Resources, Inc. IT Life Sciences Allied Healthcare CRO Certified MBE |GSA - Schedule 66 I GSA - Schedule 621I DIRECT # - 732-844-8724 Email id - seema @irionline.com| www.irionline.com LinkedIn: https://in.linkedin.com/in/seemachawhan Gold Seal JCAHO Certified ™ for Health Care Staffing “INC 5000's FASTEST GROWING, PRIVATELY HELD COMPANIES” (8th Year in a Row)

Acuren is currently recruiting for CR/DR Techs to support our operation in Denver, CO. We are seeking a highly skilled Industrial CR/DR Technician to join our non-destructive testing (NDT) team. The CR/DR Technician will operate computed radiography (CR) and digital radiography (DR) equipment to inspect materials, components, and structures for defects in industrial settings. This role requires technical expertise, adherence to safety and quality standards, and the ability to work in demanding environments such as manufacturing, aerospace, or energy sectors. State or IRRSP Card preferred, not required. Responsibilities Operate CR and DR imaging equipment to perform non-destructive testing on welds, pipelines, castings, or other industrial components. Set up and calibrate equipment to ensure accurate detection of defects, cracks, or material inconsistencies. Interpret and analyze radiographic images to identify flaws in accordance with industry standards (e.g., ASME, API, AWS). Prepare and position components or materials for inspection, ensuring proper alignment and exposure settings. Maintain and troubleshoot CR/DR systems, reporting malfunctions or calibration issues to supervisors or maintenance teams. Adhere to radiation safety regulations and protocols, including proper use of personal protective equipment (PPE) and radiation monitoring devices. Document inspection results, maintain accurate records, and generate reports for quality assurance and compliance. Collaborate with NDT supervisors, engineers, and quality control teams to ensure inspections meet project specifications. Follow strict safety and environmental guidelines, including handling and disposal of hazardous materials if applicable. Stay updated on advancements in CR/DR technology and NDT methodologies through training and certifications. Other work duties as assigned. Requirements KNOWLEDGE, SKILLS & ABILITIES: Experience with automated CR/DR systems or advanced NDT techniques (e.g., phased array, ultrasonic testing). Familiarity with quality management systems and documentation software. Basic mechanical aptitude for equipment setup and minor repairs. Strong problem-solving skills and ability to work independently or in teams. Proficiency in operating CR/DR systems, including familiarity with imaging software and analysis tools. Knowledge of radiation safety standards and industrial NDT codes (e.g., ASME, API, ASTM). Strong attention to detail and ability to interpret technical drawings and specifications. Ability to work in confined spaces, at heights, or in industrial environments with exposure to noise, dust, or extreme temperatures. EDUCATION: High school diploma or equivalent; Associate's degree or technical certification in Non-Destructive Testing, Radiographic Technology, or related field preferred. Level I or II certification in Radiographic Testing (RT) per ASNT, NAS-410, or equivalent standards. Minimum 1-2 years of experience in industrial CR/DR or NDT (entry-level candidates with relevant certifications considered). Valid driver's license and willingness to travel to job sites as needed. State or IRRSP Card preferred, not required. Benefits Competitive Salary Medical, dental, and supplemental insurance 401K Plan Paid Holidays Paid Time Off Pay Transparency:As per applicable state law the job posting pay range is $35.00-$45.00 an hour depending on experience and applicable certifications. Working Conditions Outside environment with continuous physical effort, exposure to 5-7 elements/conditions, moderate mental effort, and occasional requests for assistance. Travel may be required. PHYSICAL JOB REQUIREMENTS & DEMANDS: Lifting/carrying heavy equipment (up to 50 pounds). Standing for extended periods of time. Company Overview Acuren is a trusted, single source provider of technology-enabled asset protection solutions used to evaluate the structural integrity of critical energy, industrial and public infrastructures. Committed to delivering a Higher Level of Reliability , Acuren provides an unrivaled spectrum of capabilities including inspection, traditional and advanced NDE/NDT, failure analysis, rope access, materials engineering, field engineering, reliability engineering, drones, robotics, V-Deck and condition-based monitoring services. Our work is critical to the integrity and safety of industrial firms, including petroleum refinery, pipeline, power generation, pulp & paper, mining, pharmaceutical, aerospace and automotive industries. Acuren employs over 4,000 dedicated professionals supporting the mechanical integrity and inspection programs of the world's largest industrial segments. Acuren is a market leader. Our formula for success is straightforward: be capable locally, with certified and well-equipped personnel supported by trained, experienced leaders. Continuing to build on a strong heritage of safety, quality and professionalism, Acuren strives to maintain incident free work environments, pursues advanced technical developments, and supports reliability programs that are valued by clients and employees. #LI-YC1

Information Classification TitleTemporary Hourly Employment CategoryTemporary ?Yes Work Hours/Week0-40 Overtime Eligible?Yes Description of Work Unit Research Technicians for Tutakoke River Brant Project, Summer 2026 Search Contact Email********************** Position Summary The Department. of Fish, Wildlife, and Conservation Biology are seeking up to 2 technicians for a long-term research project on the Yukon-Kuskokwim Delta of Alaska that focuses on the evolutionary ecology, migration ecology, and population dynamics of black brant. Working hours can be irregular and are often influenced by weather and tides. The field site is on the coast of the Bering Sea and technicians will frequently be working in adverse conditions (e.g., high winds, freezing temperatures, precipitation) and walking long distances on mud flats and coastal vegetation while wearing waders. The project is based out of a remote field camp with limited amenities (e.g., no running water, cellular service, or internet). Start Date: Approximately 1 May 2026 Duration: approximately 3 Months Number of weekly working: 40 hours / week Position Minimum Qualifications Applicants must be detail oriented, and able to work both independently and cooperatively with others, and able to lift and carry >75 pounds. Preferred Qualifications Preference will be given to applicants with experience monitoring bird nests, capturing, marking, and resighting large numbers of birds, working in remote field camps, operating boats with tiller motors, operating snow machines or ATVs, and fixing small engines. Posting Details Working TitleResearch Technicians for Tutakoke River Brant Project, Summer 2026 Posting Number202500699T DepartmentFish, Wildlife and Conservation Biology Salary Range$20 per hour, depending on experience Employee Benefits Colorado State University is not just a workplace; it's a thriving community that's transforming lives and improving the human condition through world-class teaching, research, and service. With a robust benefits package, collaborative atmosphere, and focus on work-life balance, CSU is where you can thrive, grow, and make a lasting impact. + Review our detailed benefits information here. (***************************************************************************************** + Explore the additional perks of working at CSU here. + For the total value of CSU benefits in addition to wages, use our compensation calculator (******************************************************** . + Lastly, click here for more information about why Fort Collins is consistently ranked in the top cities to live in (************************************************************** ! Close Date12/31/2025 Special Instructions to Applicants To apply, please submit a single PDF with a résumé or vitae, cover letter that is less than one page, and names and contact information for three professional references by e-mail to ********************** CSU is committed to full inclusion of qualified individuals. If you are needing assistance or accommodations with the search process, please reach out to the listed search contact. References will not be contacted without prior notification to candidates. Please note, applicants may redact information from their application materials that identifies their age, date of birth, or dates of attendance at or graduation from an educational institution. Background Check Policy Statement Colorado State University strives to provide a safe study, work, and living environment for its faculty, staff, volunteers and students. To support this environment and comply with applicable laws and regulations, CSU conducts background checks for the finalist before a final offer. The type of background check conducted varies by position and can include, but is not limited to, criminal history, sex offender registry, motor vehicle history, financial history, and/or education verification. Background checks will also be conducted when required by law or contract and when, in the discretion of the University, it is reasonable and prudent to do so. EEO Colorado State University ( CSU ) provides equal employment opportunities to all applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws. Essential Job Duties Job Duty CategoryResearch Technicians for Tutakoke River Brant Project Assitance Duty/Responsibility Searching for and monitoring nests of brant and other waterfowl, reading color-character tarsal bands of marked brant, capturing and banding adult brant and goslings, data entry, and assisting with remote field camp operations. Percentage Of Time100 References Minimum References Required Maximum References Required Documents Needed To Apply Required Documents + Resume Optional Documents

At KBI Biopharma, we are advancing science and accelerating breakthroughs. As a global leader in biopharmaceutical development and manufacturing, we empower life science companies to bring new medicines and vaccines to the world faster. Explore your potential at KBI, where innovation meets impact. Position Summary: Analyst position in a growing team that supports a variety of testing in support of the manufacturing of biopharmaceutical products in a contract development and manufacturing space. Responsibilities: Supports in-process testing in support of the manufacturing of biopharmaceutical products Conducts laboratory experiments in support of biopharmaceutical development and process development including running electrophoresis gels, HPLC's and preparing buffers. Normally exercises judgment within defined procedures and practices to determine appropriate action Makes detailed observations and carries out elementary data analysis. Understands experiments and conducts troubleshooting analysis. Maintains and updates knowledge of instrumentation and maintenance. Notebook upkeep and writing skills. Maintains familiarity with current scientific literature; maintains professional expertise through familiarity with scientific literature. Assures proper labeling, handling, and storage of all chemicals used in the area; assures proper labeling and disposition of hazardous waste in satellite areas; adheres to all safety requirements and follows safe procedures, and attends all required safety and health training, including handling hazardous waste. Reacts to change productively and handles other essential tasks as assigned. Education/Experience: Research Associate II: B.A. or B.S. degree in chemistry, biochemistry or related area (or equivalent training) and 2-4 years of experience. Salary Range: $63,00 - $86,900 Salary range provided per current averages and expectations. The salary and job title for this opening will be based on the selected candidate's qualifications and experience and may be outside this range. KBI has a robust total rewards strategy which includes an annual bonus structure for all employees, medical, dental, and vision coverage, paid PTO and holidays, 401K matching with 100% vesting upon hire and employee recognition programs. About KBI: KBI Biopharma, Inc., a JSR Life Sciences company, is a global contract development and manufacturing organization (CDMO) providing fully integrated and accelerated drug development and biologics manufacturing services to life science companies. KBI supports its 500+ customers in advancing more than 160 drug candidates from preclinical and clinical stages to market, including the manufacture of ten commercial products. Recognized for quality manufacturing, KBI delivers robust process development and cGMP manufacturing services across its six global locations in the USA and Europe. For more information, visit ********************* KBI is a proud EEO/AA employer dedicated to building a diverse and inclusive workforce. We believe that innovation thrives in an environment where all voices are heard and valued. That's why we actively seek individuals from all backgrounds - regardless of race, color, national origin, religion, gender, gender identity, sexual orientation, age, disability, or veteran status - and strongly encourage all qualified candidates to apply and bring their unique perspectives to our team. KBI Biopharma, Inc. is an EEO/AA employer and actively seeks to diversify its work force. Therefore, all qualified applicants, regardless of race, color, national origin, religion, gender, gender identity, sexual orientation, age, disability or veteran status, are strongly encouraged to apply. I understand that neither the completion of this application nor any other part of my consideration for employment establishes any obligation for KBI Biopharma, Inc. to hire me. If I am hired, I understand that either KBI Biopharma, Inc. or I can terminate my employment at any time and for any reason, with or without cause and without prior notice. I understand that no representative of KBI Biopharma, Inc. has the authority to make any assurance to the contrary. I attest with my signature below that I have given to KBI Biopharma, Inc. true and complete information on this application. No requested information has been concealed. I authorize KBI Biopharma, Inc. to contact references provided for employment reference checks. If any information I have provided is untrue, or if I have concealed material information, I understand that this will constitute cause for the denial of employment or immediate dismissal.

** Applications will be received until November 10, 2025. If the position is not filled by then, we may consider applications submitted after the deadline. Interested applicants must apply online by visiting the Denver Public Schools job board at careers.dpsk12.org. ** About this job: A principal leads and manages a school, overseeing educational programs, staff, budgets, and student discipline. They ensure a safe, effective learning environment and foster strong community relationships to enhance student success. **The Principal must demonstrate a willingness to sign a confidentiality agreement. This role requires maintaining the highest level of confidentiality regarding all District matters, especially those involving the Superintendent, Chief of Staff, and the Board of Education. Ensuring trust and discretion is paramount to the success and integrity of this position. What DPS Offers You: A Culture that values Equity, Accountability, Integrity, Collaboration and Fun with a shared vision that Every Learner Thrives. Competitive Compensation and Incentive plan, click here for the DSLA Salary Schedule. For more information on compensation for these roles, click here. In addition to competitive compensation, DPS has other Total Reward offerings such as; time off, health and wellness benefits, and PERA Retirement. What You'll Do: Lead a staff of administrative, certificated and classified personnel assigned to the school. Develop plans that improve the quality and adequacy of instruction, and foster student achievement, growth and development. Research and demonstrate an understanding of, and communicate the education-based aims and needs of the community to school staff and central administration. Supervise certificated and classified staff and ensures for: professional growth and development, attainment of district and building instructional goals, implementation of curriculum, and effective use of all staff-based and facility based resources. Plan, prepare and administer the school budget, including the translation of educational needs, goals and objectives into budgetary terms. Perform other related duties, including special projects, as required or requested. What You'll Need: Hold a Bachelor's degree in education or in the subject areas for which you are applying. Hold a Master's Degree in Elementary/Secondary Education, Administration, Curriculum, Instruction or Guidance, preferred. Hold a valid Colorado Department of Education Principal License (Must be current and active while in the position). Click here for more information. Five (5) or more years of experience as an educator. Demonstrated effective and diplomatic oral and written communication skills. Lead for racial and educational excellence and work to dismantle systems of oppression and inequity in our community, along with believing in and supporting all students so they feel seen and heard with access to high quality education. Live and work with a permanent home address in Colorado while working with us. Have the ability with or without accommodations to meet the physical demands of the position. Denver Public Schools is an Equal Opportunity Employer and does not discriminate on the basis of race, color, religion, sex (including pregnancy, gender expression, and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), political affiliation, military service, or any other status protected by law or regulations. It is our intention that all qualified applicants be given equal opportunity and that selection decisions be based on job-related factors. Students First. Integrity. Equity. Collaboration. Accountability. Fun

We are recruiting for a motivated Laboratory Scientist - Microbiology to join our team! We are here for life's journey. Where is your life journey taking you? Being the heartbeat of Denver means our heart reflects something bigger than ourselves, something that connects us all: Humanity in action, Triumph in hardship, Transformation in health. Department Laboratory ServicesJob Summary Under general direction, responsible for independently accessioning, processing, performing and reporting tests analyses according to physician orders and in accordance with laboratory policies and procedures, FDA, TJC CLIA, OSHA regulations to facilitate optimum quality patient care. The employee determines that test results meet requirements of the quality control program and if not met, repeats test and ensures results are accurate before reporting. Employee reports test results following department policy, maintaining all necessary documentation and records. Essential Functions: Performs maintenance and testing in an independent manner under supervision of an MLS/Medical Technologist or (15%) Supervisor by utilizing procedure manuals, operator manuals, instrument hotlines, etc. to problem solve. (15%) Analyzes pre-analytical, analytical and post-analytical quality control and specimen requirements to ensure quality and accurate results. (10%) Documents and resolves all quality issues to ensure accurate patient test resulting. (10%) Analyzes problems or instrument malfunctions prior to release of patient results in a thorough, effective and timely manner. (10%) Follows safety, life safety, and infection control procedures for self, patients, and others at all times. (10%) Follows safe chemical, BBP, hand hygiene, and work practices to ensure Environment of Care (EOC) is maintained. (10%) Participates in required competency, continuing education, and proficiency testing meeting timeline requirements for all departments worked. (10%) Participates in mentoring, training, and teaching new staff, students, and residents in the laboratory, to educate the next generation of healthcare professionals. (10%) Education: Bachelor's Degree chemistry, biology, biochemistry, microbiology, molecular or other laboratory science related area. Required Work Experience: less than 1 year Previous experience in a medical laboratory preferred. Licenses: Knowledge, Skills and Abilities: Knowledge of quality control requirements to ensure pre-analytical, analytical, and post-analytical quality results. Skilled in analyzing specimens utilizing instrument platforms, testing kits, and manual procedures according to department policy. Ability to log and perform all required maintenance and trouble-shoot equipment and problems to completion and consult with a supervisor when required. Ability to meet turn-around times to ensure timely patient testing. Ability to troubleshoot testing and quality issues with technology. Shift Work Type PRN/Intermittent Salary $25.00 - $37.50 / hr Benefits Social security replacement retirement plan with employer contribution of 3% On-site employee fitness center and wellness classes Community resource navigation support Childcare discount programs & exclusive perks on large brands, travel, and more Education & development opportunities including career pathways and coaching Our Values Respect Belonging Accountability Transparency All job applicants for safety-sensitive positions must pass a pre-employment drug test, once a conditional offer of employment has been made. Denver Health is an integrated, high-quality academic health care system considered a model for the nation that includes a Level I Trauma Center, a 555-bed acute care medical center, Denver's 911 emergency medical response system, 10 family health centers, 19 school-based health centers, Rocky Mountain Poison & Drug Safety, a Public Health Institute, an HMO and The Denver Health Foundation. As Colorado's primary, and essential, safety-net institution, Denver Health is a mission-driven organization that has provided billions in uncompensated care for the uninsured. Denver Health is viewed as an Anchor Institution for the community, focusing on hiring and purchasing locally as applicable, serving as a pillar for community needs, and caring for more than 185,000 individuals and 67,000 children a year. Located near downtown Denver, Denver Health is just minutes away from many of the cultural and recreational activities Denver has to offer. Denver Health is an equal opportunity employer (EOE). We value the unique ideas, talents and contributions reflective of the needs of our community. Applicants will be considered until the position is filled.

Job Description Job Title: Embryologist Reports to: Lead Embryologist FLSA Status: Exempt Summary: CNY Fertility is a renowned fertility center offering advanced treatments like IVF, IUI, and egg freezing. With a patient-centered approach and cutting-edge technology, we support individuals and couples on their journey to parenthood. Our Senior Embryologist will be detail-oriented, team player, technically skilled and highly motivated to carry out the mission of CNY Fertility. Required Duties and Responsibilities: Include the following. Other duties may be assigned. Daily quality control, media preparation and dish preparation. Microscope and pipettor use. Use of other lab equipment to complete procedures: balance, pH meter, CO2 monitor, labeler etc. Oocyte retrieval and denuding of oocytes. Embryo and oocyte thawing/embryo and oocyte freezing. Fertilization checks and embryo transfers. Have a well-developed understanding of all aspects of running an Embryology lab including but not limited to: equipment maintenance and troubleshooting, QC/QA/QM/QI. ICSI and conventional fertilization techniques. Schedule procedures, complete tasks and navigate patient charts. Understanding of cryopreservation and storage specimens. Assist in cleaning and stocking inventory for the laboratory. Perform PGT and load samples. Ability to interpret PGT reports and call patients with results. Communicate with patients across various platforms such as web correspondences and phone calls. Perform PESA/TESE sperm retrievals. Participate in the alarm response team. Qualifications: To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Education/Experience: Bachelor's degree in biology, or related field. At least four years of experience in clinical embryology setting required. Language Ability: 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. Math Ability: Ability to add, subtract, multiply, and divide in all units of measure, using whole numbers, common fractions, and decimals. Ability to compute rate, ratio, and percentage and to draw and interpret bar graphs. Reasoning Ability: Ability to solve practical problems and deal with a variety of concrete variables in situations where only limited standardization exists. The ability to interpret a variety of instructions furnished in written, oral, diagram, or schedule form. Knowledge, Skills and Other Abilities: Excellent oral and written communication skills. Must be able to lift 25lbs. Excellent computer literacy. Adequate vision or corrective lenes for sample identification. Ability to multitask in fast paced environments. Work Environment: The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. There is some risk of exposure of bodily fluids or contagious diseases. Weekend and holiday rotation is required. 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. While performing the duties of this job, the employee is regularly required to stand; walk; use hands; reach with hands and arms and talk or hear. The employee is occasionally required to sit. Benefits include: · 401(k) · Dental insurance · Vision Insurance · Health Insurance · Life Insurance · Flexible spending account · Paid time off · Maternity Leave

To perform, specific analysis/assays in the clinical laboratory under the direction of the supervisor as an entry level laboratory scientist. To produce accurate tests results for all patients and perform the following essential responsibilities. Essential Duties Performs high complexity tests that are authorized by the laboratory leadership. Adheres to and understands the laboratory's quality control policies documenting all quality control activities, instrument and procedural calibrations and maintenance performed. Follows set guidelines to troubleshoot/correct assay problems or instrument malfunctions. Performs maintenance and works with supervisor in troubleshooting QC or instrument problems. Follows the laboratory's and NJH established policies and procedure manuals. Reviews and signs laboratory and personnel SOP on an annual basis. Is responsible for completing NetLearning in a timely manner. Follows specific biosafety standards for the laboratory and protocols for handling potentially infectious material. Performs error correction, data entry and compilation of data packets as required. Documents all corrective actions taken when test systems deviate from the laboratory's established performance specifications. Participates and maintains records that demonstrate that proficiency testing samples are tested in the same manner as patient specimens. Follows GxP (e.g., GLP, GCLP, GCP, etc.) standards as defined by different national and international organizations (e.g., ISO, FDA, OECD, etc.) when appropriate. Performs competencies (including age-specific competencies and/or non-human species) as identified through the departmental competency program. Appropriately uses the computer systems in the department, including proper use of order/reports/charging, and maximizes personal proficiency. Responds appropriately to email and other forms of communication in a timely manner. Monitors and reports on stocks of supplies and equipment, as directed. Makes reagents as necessary. Participates in preparation for inspections where required. Attends continuing education programs sponsored by National Jewish Health, manufacturer in-services and/or professional society programs. Makes efforts to obtain at least 12 CEU credits per year including but not limited to the following: webinars, lunch and learn seminars, seminars, etc. Competencies Accountability: Accepts full responsibility for self and contribution as a team member; displays honesty and truthfulness; confronts problems quickly; displays a strong commitment to organizational success and inspires others to commit to goals; demonstrates a commitment to National Jewish Health. Laboratory Knowledge: Clearly discusses scientific principle behind laboratory testing; understands functional mission, own job requirements and impact on the organization. Customer Focus: Will look at processes and results with the laboratory in mind; understand organizational roles and associated functions; maintains personal integrity, admits mistakes, and keeps promises; follows up on promises to ensure accuracy and timeliness of fulfillment; takes personal responsibility for correcting customer or physician problems; recognizes the importance of maintaining customer and physician relationships; all work is conducted in the spirit of “what's in it for the customer or patient.” Decision Quality: Exhibits one-dimensional decisions that are advantageous to either the laboratory or the patient; comfortable making decisions with lots of consensus; knows when they can make decisions independently. Drive for Results: Can identify own mistakes and proactively fixes when identified; productivity is at expectations; adapts to personnel changes and shifts in laboratory environment; will regularly take on new initiatives as directed. Informing Communicating: Addresses issues as they arise or within an appropriate time interval; effectively uses all forms of communication; informs coworkers/leadership of when work product may be affected. Managing Change: Maintains open mind and willingness to try new ideas or approaches; analyzes both success and failure to determine how to improve; has a desire to learn. Professional Relationships: Quickly establishes and maintains rapport and credibility with laboratory team; respects differing opinions and viewpoints; is consistently polite and courteous to others; performs work in team setting and contributes to the success of the team in a meaningful way; maintains personal integrity, admits mistakes, and keeps promises; maintains a positive attitude. Problem Solving: Collects and organizes data before initiating analysis and asks questions to prioritize key issues; identifies inconsistent details within SOPs or processes; able to work through immediate problem with assistance. Supervisory or Managerial Responsibility None Travel None Core Values Be available to work as scheduled and report to work on time. Be willing to accept supervision and work well with others. Be well groomed, appropriately for your role and wear ID Badge visibly. Be in compliance with all departmental and institutional policies, the Employee Handbook, Code of Conduct and completes NetLearning by due date annually. Promotes a workplace culture based on mutual respect and merit, where all individuals are treated fairly and provided with equal opportunity to contribute to the mission and goals of the institution. Adheres to safe working practices and at all times follows all institutional and departmental safety policies and procedures. Wears appropriate PPE as outlined by the infection control policies and procedures. Demonstrates compliance with all state, federal and all other regulatory agency requirements. Minimum Qualifications Education: Bachelors of Science degree in biology, chemistry or a related scientific field required. Work Experience: Previous laboratory experience preferred. Special Training, Certification or Licensure: None Salary Range: $22.76 - $30.10 Benefits At National Jewish Health, we recognize that our outstanding faculty and staff are the essence of our organization. For every aspect of health care, our employees are our greatest asset. With that in mind, we have designed a valuable, comprehensive benefits package to meet the needs of our employees and their families. Comprehensive Medical Coverage: Multiple Cigna health plans for Colorado, regional office and remote employees. Health Savings Accounts (HSA) and Flexible Spending Accounts (FSA) available to pair with some plans. Paid Time Off: Generous PTO accruals to use for vacation and sick days, and six paid holidays, all compliant with Colorado state sick leave regulations. Dental & Vision Plans: Coverage effective the first of the month after hire. Retirement Savings: 403(b) plan with employer contributions after two years. Wellness Incentives: Earn up to $200 annually for preventive health activities. Tuition Reimbursement: Up to $5,250 annually for full-time and part-time employees. Child Care Assistance: Childcare Flex Spending Account (FSA) with annual employer contribution. Loan Forgiveness: Public Service Loan Forgiveness (PSLF) eligible employer. Disability & Life Insurance: Employer-paid plans and optional buy-up choices. Voluntary Benefits: Full suite of coverage options such as Accident, Hospital Indemnity and Legal Plan Exclusive Discounts: Savings on local services, insurance, and RTD bus passes. Anticipated Application Deadline: 2025-10-17

Open Fertility is committed to making exceptional fertility care accessible to more people than ever. From egg freezing to IVF, we simplify and streamline treatments so patients can pursue their reproductive goals with confidence. We're looking for passionate, driven individuals who want to make a meaningful impact in people's lives. As part of our rapidly growing team, you'll help innovate fertility care and transform the patient experience. Our clinics are currently open in Roseville, CA and Astoria, NY, with Denver, CO coming soon. Our Core Values: Open Possibilities: Helping patients achieve their reproductive goals. Open Access: Making high-quality fertility care available to those paying out of pocket. Open Arms: Welcoming every patient with compassion and understanding. Role Summary This position is responsible for performing high quality IVF laboratory medical procedures. The embryologist consults and advises other staff groups/members regarding IVF laboratory procedures and outcomes, and human assisted reproductive techniques (ART). The embryologist works in a collaborative relationship with the IVF Laboratory Supervisor and other team members, as well as with other Spring Fertility departments as needed. The Embryologist are required to rotate in Andrology/Endocrinology laboratory as needed to cover or help as needed. The Embryologist position requires the candidate to be proficient and independent in all basic and advanced IVF laboratory procedures. Day to day duties include: Provide high quality service to couples seeking treatment for infertility, including diagnostic and therapeutic services. Conducts the full range of basic and advance ART laboratory procedure under the direction of the Laboratory Director Works together with Laboratory Director to coordinate work for an effective use of resources. Works collaboratively with the IVF Laboratory Director and the IVF team to proactively identify evolving “best practices” as well as area of improvement in the Laboratory process and department operations. Complies with regulations and laws for human ART in U.S. and California, adheres to the policy and rules of SPRING Fertility, and assures that works is performed in accordance with ASRM standards. Scrupulously follows laboratory and clinic SOPs as well as comply with all safety policies and standards. Meets quality standards and numerical goals for laboratory procedures, as set by Laboratory Director. Conducts at required standards all the ART tasks, including but not limited to the following procedure: ICSI (be at same level with other embryologist for fertilization rate 90%), biopsy (70% implantation rate and 95% survival rate), media and dishes set up, eggs retrievals, sperm preparation, eggs inseminations, fertilization checks, stripping of cumulus cells for ICSI procedure, embryo grading (Gardner grading), participates in PT external and internal, successfully performs embryo transfers of fresh and frozen embryos. Communicate effectively and compassionately with patients and other SPRING Fertility team members. Conducts daily quality control activities Performs all ancillaries' duties as request to maintain a clean and operating laboratory, including cleaning, equipment maintenance and inventory control. Education, Licenses, Certifications Bachelors in Science in Biological or Chemistry required; degree in reproductive Biology preferred Technical Supervisor certification from the American Board of Bioanalysis (ABB) within two years from when eligible. Minimum of 5 years of experience in embryology field. Good command of written and spoken English. Employment Type This is a full time exempt onsite position that requires early hours, rotating weekends and holidays. Compensation The salary range for this role is 70,000-150,000. Salary is based on several factors including job related knowledge and skill set level for embryology, depth of experience, certifications and/or degrees. Benefits Investing in you today Competitive Medical, Dental, and Vision Plans Paid Time Off to enjoy “you” time! Additional benefits - Commuter Benefits, Discounted rates on home, auto and pet insurance Investing in your future 401k Match with up to 4% matching Fertility Benefits Discount Program Paid Life and Disability Insurance Don't have it all? We still welcome you to apply! At Open Fertility, we believe that everyone who wants a family deserves to have one, regardless of gender, sexual orientation, race, ethnicity, or religion. Just as we acknowledge and value the diversity of goals, life experiences, and unique paths to parenthood among our patients, we also actively celebrate diversity within our organization. We are an equal opportunity employer, and we are committed to a safe and inclusive work environment for all. We recognize that diversity among our team allows us to not only more effectively serve our patients, but also to advance innovation and opportunity within our field. We encourage qualified applicants of every background, ability, and life experience to apply to our employment opportunities. The Human Resources Department will make reasonable efforts in the recruitment process to accommodate applicants with disabilities. If selected for an interview, and you require accommodation, please notify the recruiter who reached out to you. If you need assistance in navigating our website and the job application process, please email us at ****************************** CCPA disclosure notice here.

Kindbody is the leading fertility clinic network and global family-building benefits provider for employers offering the full-spectrum of reproductive care from preconception to postpartum through menopause. Kindbody is the trusted fertility benefits provider for 132 leading employers, covering almost 2.9 million lives. As the fertility benefits provider, technology platform, and direct provider of care, Kindbody delivers a seamless, integrated experience with superior health outcomes at lower cost, making fertility care more affordable and accessible for all. Kindbody has raised $315 million in debt and equity funding from leading investors including Perceptive Advisors, JP Morgan Chase's Morgan Health, GV (formerly Google Ventures), RRE Ventures, Claritas Health Ventures, Rock Springs Capital, Distributed Ventures, Whatif Ventures and TQ Ventures. Visit ***************** and follow us on Instagram, Twitter, and Linkedin. Kindbody's clinically-managed program covers the full-spectrum of reproductive health, including both female and male fertility, which encompasses fertility assessments and education, fertility preservation, genetic testing, in vitro fertilization (IVF), donor and surrogacy services, and adoption, as well as a full continuum of reproductive care including physical, mental, and emotional support. About the Role As an experienced Senior Embryologist reporting to our Lab Managers in various locations, you will be working in a fast-paced, rapidly growing environment where you will be relied on for your expertise, professionalism, and collaboration. Proposed Schedule: 18 days per month in lab (travel day included) and 1 week remote admin work, subject to change based on the needs of the business. Responsibilities Perform assisted reproductive technology methods including, but not limited to, semen preparation, oocyte identification conventional IVF, ICSI, embryo culture and grading, laser assisted hatching, trophectoderm biopsy, sperm, oocyte and embryo cryopreservation (vitrification). Maintain accurate laboratory records Perform quality control procedures and monitor KPIs Participate in the laboratory's quality management program Coordinate with reproductive endocrinologists and OB/GYNs to assist their patients with reproductive health issues and clinical research. Educate patients on infertility evaluations, medications, treatment protocols and procedures Provide patient/couple counseling, procedure teaching, communicates physician orders and instructions Ensure all patient information is documented appropriately in our EMR according to our procedures Works independently to assure the program goals are achieved Support and promote excellence in customer service Provide feedback to HQ on process improvement and job specifications to help gain efficiencies in the day to day Who You Are Willingness to be flexible and travel nationwide to any of our 20 clinics 6+ years experience in clinical embryology {3-4 of which are micromanipulation} Able to work independently with minimal supervision Proficiency in all IVF laboratory methods including micromanipulation techniques and vitrification Detail oriented, meticulous record-keeping Strong communication skills & a team player Familiarity with all state and local regulations including tissue bank licensing Experienced in EMR and G-Suite

**University of Colorado Anschutz Medical Campus** **Department:** **Immunology and Microbiology** **Job Title:** **Laboratory Science Professional** #:** **00841242 - Requisition #:** **38093** Key Responsibilities: + Utilize a variety of laboratory techniques required for research projects. + Perform experiments and tabulate and analyze research findings. **Work Location:** Onsite **Why Join Us:** **Why work for the University?** + Medical: Multiple plan options + Dental: Multiple plan options + Additional Insurance: Disability, Life, Vision + Retirement 401(a) Plan: Employer contributes 10% of your gross pay + Paid Time Off: Accruals over the year + Vacation Days: 22/year (maximum accrual 352 hours) + Sick Days: 15/year (unlimited maximum accrual) + Holiday Days: 10/year + Tuition Benefit: Employees have access to this benefit on all CU campuses + ECO Pass: Reduced rate RTD Bus and light rail service **Qualifications:** **Minimum Qualifications:** + Bachelor's degree in biology, molecular biology, chemistry, genetics or related field + One (1) year professional-level research experience. + The candidate must have experience with animal studies, immunological assays, and cell culture-based assays. Substitution **Preferred Qualifications:** + Master's degree in biology, molecular biology, chemistry, genetics or related field + Two (2) years of experience in an experimental or wet laboratory. The candidate must have experience with animal studies, immunological assays, and cell culture-based assays. **Knowledge, Skills and Abilities:** + Knowledge of basic laboratory safety procedures. + Experience with animal studies, immunological assays, and cell culture-based assays. + Ability to communicate effectively, both in writing and orally. + Ability to establish and maintain effective working relationships with + employees at all levels throughout the laboratory and institution + Ability to interpret and master complex research protocol information **How to Apply:** **Screening of Applications Begins:** **Anticipated Pay Range:** **HIRING RANGE** **$50,357 - $64,054** **Equal Employment Opportunity Statement:** **ADA Statement:** **Background Check Statement:** **Vaccination Statement:** **Job Category** **Primary Location** **Schedule** **Posting Date** **Unposting Date** **To apply, visit ******************************************************************** (****************************** Copyright 2025 Jobelephant.com Inc. All rights reserved. Posted by the FREE value-added recruitment advertising agency (***************************** Laboratory Science Professional - 38093 University Staff The Morrison Laboratory at the University of Colorado Anschutz Medical Campus is a dynamic, fast-paced research laboratory focused on viral immunology and medical countermeasure development (i.e., therapeutics and vaccines). We seek a new team member to take a lead role in performing cutting-edge experimental science. This is an exciting opportunity to join a fantastic group of scientists and develop key research skills. In addition, opportunities exist to learn state-of-the-art research techniques at the forefront of immunological and infectious disease research. - this role is expected to work onsite and is located in Aurora, Colorado. The Department of Immunology and Microbiology is a highly collaborative group of scientists committed to the performance of rigorous research that improves human health. We support the career development of all our staff with numerous opportunities to gain new knowledge and skills. We have AMAZING benefits and offerexceptional amounts of holiday, vacation and sick leave! The University of Colorado offers an excellent benefits package including: There are many additional perks & programs with the CU Advantage (******************************************************* URL=************************** . : Or a combination of education and related technical/paraprofessional experience may be substituted for the bachelor's degree on a year-for-year basis Applicants must meet minimum qualifications at the time of hire. For full consideration, please submit the following document(s):1. A letter of interest describing relevant job experiences as they relate to listed job qualifications and interest in the position2. Curriculum vitae / Resume3. Three to five professional references, including name, address, phone number (mobile number if appropriate), and email address Questions should be directed to: Thomas E. "Tem" Morrison; ****************************** (******************************************************* URL=******************************) Immediately and continues until position is filled. For best consideration, apply by January 22, 2025. The starting salary range (or hiring range) for this position has been established as The above salary range (or hiring range) represents the University's good faith and reasonable estimate of the range of possible compensation at the time of posting. This position may be eligible for overtime compensation, depending on the level.Your total compensation goes beyond the number on your paycheck. The University of Colorado provides generous leave, health plans and retirement contributions that add to your bottom line.Total Compensation Calculator (******************************************************* URL=****************************** CU is an Equal Opportunity Employer and complies with all applicable federal, state, and local laws governing nondiscrimination in employment. We are committed to creating a workplace where all individuals are treated with respect and dignity, and we encourage individuals from all backgrounds to apply, including protected veterans and individuals with disabilities. The University will provide reasonable accommodations to applicants with disabilities throughout the employment application process. To request an accommodation pursuant to the Americans with Disabilities Act, please contact the Human Resources ADA Coordinator at ******************************** (******************************************************* URL=********************************) . The University of Colorado Anschutz Medical Campus is dedicated to ensuring a safe and secure environment for our faculty, staff, students and visitors. To assist in achieving that goal, we conduct background investigations for all prospective employees. CU Anschutz strongly encourages vaccination against the COVID-19 virus and other vaccine preventable diseases (******************************************************* URL=*********************************************************************************** . If you work, visit, or volunteer in healthcare facilities or clinics operated by our affiliated hospital or clinical partners or by CU Anschutz, you will be required to comply with the vaccination and medical surveillance policies of the facilities or clinics where you work, visit, or volunteer, respectively. In addition, if you work in certain research areas or perform certain safety sensitive job duties, you must enroll in the occupational health medical surveillance program (******************************************************* URL=************************************************************************************* . Application Materials Required: Cover Letter, Resume/CV, List of References : Research Services : Aurora Department: U0001 -- Anschutz Med Campus or Denver - 21577 - SOM-IMM MICRO GENERAL OPER : Full-time : Oct 22, 2025 : Ongoing Posting Contact Name: : Thomas E. "Tem" Morrison; Posting Contact Email: ****************************** (******************************************************* URL=******************************) Position Number: 00841242jeid-529a911255b30c42b0611d0ed70b7c66 The University of Colorado does not discriminate on the basis of race, color, national origin, sex, age, pregnancy, disability, creed, religion, sexual orientation, gender identity, gender expression, veteran status, political affiliation, or political philosophy. All qualified individuals are encouraged to apply.

Full-time Description At SPL, we turn science into impact. We're searching for a detail-oriented Sample Management Technician to join our laboratory team in Commerce City, CO. In this role, you'll handle the intake, documentation, and organization of environmental samples to support compliance and decision-making. From logging samples into the Laboratory Information Management System (LIMS) to overseeing storage and distribution, your work ensures accuracy, efficiency, and integrity across the lab. If you're reliable, organized, and eager to learn in a fast-paced laboratory setting, we'd love to hear from you! Why You'll Love This Role Contribute to the accurate intake, tracking, and organization of environmental samples; Build hands-on skills across a variety of lab support areas, including inventory, storage, distribution, and shipping; Work closely with teammates to keep daily lab operations running smoothly and safely; Help drive efficiency, reliability, and overall success within the laboratory. What You'll Do Receive and document samples from clients, couriers, shipping, laboratory, and/or field staff; Verify that all samples meet condition standards and comply with organizational policies, quality requirements, and applicable regulatory guidelines; Accurately record sample information, details, and required analyses in laboratory software system; Label, organize, and distribute samples to appropriate personnel in a timely manner; Maintain orderly and secure sample storage areas and oversee the proper placement, retrieval, and disposal of samples in accordance with established protocols; Prepare sample kits and manage outbound shipments as required; Provide assistance to colleagues and support related operational functions, including inventory management, supply preparation, and general support activities; Perform other duties as assigned. Requirements What Makes You a Great Fit High School Diploma or equivalent required; Basic computer skills, including database and spreadsheet entry; Strong recordkeeping skills with attention to detail; Effective organizational and multitasking abilities, with the capacity to perform under pressure; Strong communication skills and ability to work both independently and collaboratively. The Perks of Being Part of Our Team Grow Your Future: 401(k) plan with company matching to boost your retirement savings; Health & Wellness Covered: Comprehensive dental, vision, and health insurance plans; Spend Smart, Live Well: Flexible HSA and FSA accounts to help manage healthcare costs; Safety Net On Us: Employer-paid short-term and long-term disability coverage; Celebrate & Recharge: 9 paid holidays plus a generous PTO plan to balance work and life; Extra Protection: Employer-paid voluntary life and AD&D insurance; Family First: Paid parental leave available for both parents; Support When You Need It: Employee Assistance Program (EAP) for personal and professional help; Exclusive Perks: Discounts on products, services, and experiences just for you. Your Schedule and The Fine Print Full-time position following a standard Monday-Friday schedule; Must be able to work outside of scheduled hours, including evenings or weekends, as required to meet operational or workload needs. Our Commitment to Diversity and Inclusion At SPL, we believe that a diverse team is a strong team. We are proud to be an equal opportunity employer, committed to creating an inclusive environment where all employees can thrive. We make all employment decisions based on qualifications, merit, and business needs, without regard to race, color, religion, sex, gender identity or expression, sexual orientation, national origin, age, disability, veteran status, or any other legally protected characteristic. We are also committed to providing reasonable accommodations to applicants and employees with disabilities or for sincerely held religious beliefs, in accordance with applicable laws. If you need assistance or an accommodation during the application process, please let us know. Visa Sponsorship At this time, SPL is not able to offer visa sponsorship for this position. We sincerely appreciate your interest and understanding, and we encourage you to explore other opportunities with us that may be a fit in the future. Salary Description $20-$23 per hour

Kelly Science & Clinical is seeking a **Research Associate - Process Analytics** for a **contract** position at a cutting-edge **Client** in **Louisville, CO** . If you're passionate about bringing the latest scientific discoveries to life and are ready to take the next step in your career, trust The Experts at Hiring Experts. **Pay:** $61,200 - $75,600 **Schedule:** Full-time Onsite Mon-Fri **Overview** Client is a game-changing biotech start-up focused on transforming the treatment of cancer with a novel integrated immunotherapy platform. Their vision is to develop off-the-shelf therapies capable of treating any tumor, any time. This position plays a critical role in advancing Client's pipeline and analytical development capabilities. The Research Associate will support characterization of Lentiviral Vector (LVV) and work closely with other functions to test LVV samples. **Responsibilities:** + Assist with method design, execution, and analysis to support development of gene therapy products + Perform routine impurity and characterization testing (e.g., ELISA, qPCR, dd PCR, flow cytometry) to support process development + Maintain clear records of experimental work using an electronic notebook system that adheres to company guidelines + Manage sample submissions in Benchling for assigned methods and ensure timely data turnaround + Exemplify company core values and adhere to policies to ensure safety and quality of gene therapy products and facility **Qualifications:** + BS in Biology, Biochemistry, or related discipline with no previous working experience OR Associate's Degree and 2 years of hands-on laboratory experience (equivalent combinations of education and experience considered) + Hands-on experience with one or more of the following techniques: dd PCR, qPCR, ELISA, and flow cytometry **Preferred Qualifications:** + Excellent communication skills and ability to work collaboratively in a multidisciplinary team + Experience with basic data analysis is a plus + Self-motivated, organized, and clear documentation skills + Ability to work in a fast-paced environment, meet deadlines, and prioritize multiple projects **Physical Requirements:** + 100% compliance with PPE requirements in laboratory environments + Ability to perform physical tasks including standing, walking, bending, kneeling, and occasionally lifting up to 50 lbs + Regular on-site presence required for analytical development and execution **What happens next:** Once you apply, you'll proceed to next steps if your skills and experience look like a good fit. But don't worry - even if this position doesn't work out, you're still in our network. That means our team of expert Science & Clinical recruiters will have access to your profile, making your opportunities limitless. p#! As part of our promise to talent, Kelly supports those who work with us through a variety of benefits, perks, and work-related resources. Kelly offers eligible employees voluntary benefit plans including medical, dental, vision, telemedicine, term life, whole life, accident insurance, critical illness, a legal plan, and short-term disability. As a Kelly employee, you will have access to a retirement savings plan, service bonus and holiday pay plans (earn up to eight paid holidays per benefit year), and a transit spending account. In addition, employees are entitled to earn paid sick leave under the applicable state or local plan. Click here (********************************************************************* for more information on benefits and perks that may be available to you as a member of the Kelly Talent Community. Why Kelly Science & Clinical? Kelly Science & Clinical is your connection to premier scientific and clinical companies looking to hire industry experts just like you. Our team creates expert talent solutions to solve the world's most critical challenges. Every day, we match science professionals with dream jobs that fit their skills, interests, and career goals-it's the way we think job searching should be. Nearly 100 percent of our science recruiters have a professional background and education in science, so we know a thing or two about the science market and how to get your expertise noticed. About Kelly Work changes everything. And at Kelly, we're obsessed with where it can take you. To us, it's about more than simply accepting your next job opportunity. It's the fuel that powers every next step of your life. It's the ripple effect that changes and improves everything for your family, your community, and the world. Which is why, here at Kelly, we are dedicated to providing you with limitless opportunities to enrich your life-just ask the 300,000 people we employ each year. Kelly is committed to providing equal employment opportunities to all qualified employees and applicants regardless of race, color, sex, sexual orientation, gender identity, religion, national origin, disability, veteran status, age, marital status, pregnancy, genetic information, or any other legally protected status, and we take affirmative action to recruit, employ, and advance qualified individuals with disabilities and protected veterans in the workforce. Requests for accommodation related to our application process can be directed to the Kelly Human Resource Knowledge Center. Kelly complies with the requirements of California's state and local Fair Chance laws. A conviction does not automatically bar individuals from employment. Kelly participates in E-Verify and will provide the federal government with your Form I-9 information to confirm that you are authorized to work in the U.S. Kelly Services is proud to be an Equal Employment Opportunity and Affirmative Action employer. We welcome, value, and embrace diversity at all levels and are committed to building a team that is inclusive of a variety of backgrounds, communities, perspectives, and abilities. At Kelly, we believe that the more inclusive we are, the better services we can provide. Requests for accommodation related to our application process can be directed to Kelly's Human Resource Knowledge Center. Kelly complies with the requirements of California's state and local Fair Chance laws. A conviction does not automatically bar individuals from employment.

Job Description About Summit Pathology: Located in Loveland, CO, Summit Pathology Laboratories is an independent pathology laboratory serving hospital systems and physician offices in Colorado, Wyoming and Nebraska. We take pride in providing outstanding general surgical pathology, as well as, world class expertise in additional areas such as breast pathology, cytopathology, hematopathology, gastrointestinal pathology and dermatopathology. Summit Pathology provides state of the art disease detection and exceptional customer service Job Summary Summit Pathology in Loveland, CO has an opportunity for a qualified Histologist to become part of our team of dedicated professionals.. Responsibilities and Duties Embedding, microtomy, special staining, immunohistochemistry and equipment maintenance to assure timely and high quality preparation of histology specimens Applicants will demonstrate competency in using multiple computer systems, practice excellent customer service skills, be willing to work any shift, and demonstrate independent judgement. Qualifications and Skills Two years' experience at the bench level New Graduate from a Histology Program will be considered ASCP Certification, preferred Must have strong mental and visual concentration Good hand/eye coordination. Strong interpersonal skills with emphasis on communication Starting pay range for this position: $27-$35 per hour depending on experience and qualifications. Benefits for a full-time employee are as follows: Five (5) Medical Insurance options by Cigna Four (4) Dental Insurance options by Cigna Vision Insurance by Cigna 401 K by Ascensus Benefit offerings by ID Shield - Identity Theft Protection, Legal Shield - Legal Protection, TeleHealth Paid Time Off & Holiday Pay Powered by JazzHR 6xC9Rz94GG

Job DescriptionSalary: $21.00 USD to $23.00 USD Probi USA is a dynamic and rapidly expanding manufacturing company based in Lafayette, CO. With a reputation for excellence in producing probiotics and nutritional supplements, Probi USA serves as a trusted contract manufacturer for numerous esteemed private labels and brands worldwide. Our dedicated team of employees shares a commitment to delivering top-tier nutraceutical products to the market. Position Summary: The Microbiology Technician conducts microbiological and laboratory analyses, ensuring compliance with Good Laboratory Practices (GLP). Responsibilities include calibrations, verifications, sample preparation and tracking, out-of-specification (OOS) investigations, and continuous improvement initiatives. The role requires effective workload planning and collaboration with laboratory and production teams to deliver timely, high-quality results. The technician also supports quality operations on the manufacturing floor. Schedule: Sunday - Thursday 7:00 a.m. to 3:30 p.m. MST, or Tuesday - Saturday 7:00 a.m. to 3:30 p.m. Key Job Duties: Perform microbiological and physical analyses of raw, in-process, and finished materials (GMP environment) Maintain and restock laboratory supplies Conduct stability testing and prepare media Record and archive analytical results (paper/electronic) Monitor cold storage, incubators, and stability chambers; escalate issues as needed Manage environmental monitoring programs and documentation (GMP/GLP) Maintain a clean, organized laboratory (inventory control, sanitation) Review and update Standard Operating Procedures (SOPs) Coordinate sample submissions to internal and third-party labs Support raw material sampling and release documentation Assist with quality systems monitoring (ATP/allergen, scale verifications, temperature monitoring, production line clearance) Undertake additional duties or special projects assigned. Proactively identify and suggest process improvements Company Requirements: Microbiology laboratory techniques and GMP/GLP compliance Analytical and problem-solving skills Attention to detail and accuracy in documentation Effective workload planning and time management Collaboration and communication within cross-functional teams Advanced computer proficiency (Microsoft Office Suite; ERP/QMS systems) Ability to work independently and as part of a team Experience with quality tools (five-why analysis, flow charts, check sheets) Basic equipment maintenance and troubleshooting skills Adaptability to new systems and processes Must be able to work safely in laboratory and manufacturing environments and ensure the safety of others. Must be comfortable around heavy equipment and be able to lift 40 lbs. Able to adhere to strict confidentiality policies and procedures. Ability to read, write, and converse in the English language. Must follow GMP/GLP, PPE, and company safety policies in the performance of job duties. Must maintain good attendance. Able to pass a background check. Work Experience and Education Requirements: Bachelors degree in microbiology/biology, or other related science, or 10+ years of progressive experience related to microbiology analysis Minimum 1 year experience in GMP microbiology laboratory BENEFITS FOR US EMPLOYEES Medical, vision, and dental coverage after 30 days (and first day of the following month) with approximately85% being paid by employer. Three (3) plans to choose from. Long-term and short-term disability insurance at no cost to employee. PTO (Paid Time Off) accrues on hire with up to 4 weeks (20 days) for new hire and increases the longer you are with the company. Participation in the company 401(K) and Roth plan after 6 months of employment with up to 4% employer match. Nine (9) paid holidays. 17 hour per calendar year to volunteer in the community. $100 Wellness dollars per year. Free daily uniforms, safety shoe vouchers. Employee Referral Bonus Tuition Reimbursement Monthly birthday and anniversary celebrations. Team-building events throughout the year including summer and winter celebrations. If you meet these qualifications and are eager to join a dynamic team dedicated to excellence in manufacturing, we encourage you to apply for the Process Engineer position at Probi USA. We look forward to welcoming a talented individual who shares our passion for quality and innovation. At Probi USA, we believe hiring should be fair, objective, and centered around helping candidates succeed. Thats why we have partnered with Alva Labs to use science-based and fair assessments. The Psychometric Assessments from, Alva Labs help us understand key traitssuch as logic and personalitythat contribute to success in this role. Many Candidates tell us they enjoy taking these assessments as it gives them personal insights on how they naturally work and help support why they would fit in a role that is fair and unbiased. Please watch for an email from Alva Labs with your assessment link. Completing the assessment is required to move forward in our process. Thank you for taking this important step with us! Probi USA is an Equal Employment Opportunity (EEO)/Affirmative Action Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, national origin, age, disability, marital status, veteran status or any other protected factor. IND123

Vantage Hemp is a private startup company that has established a world-class large-scale hemp extraction facility in Greeley, CO. The company aims to become a key player in the rapidly growing CBD Industry and plans to expand quickly using cutting-edge extraction technology. Position Summary: This is a hands-on, full-time position with duties that include playing an integral role in the research and development, troubleshooting of large scale production and development of new products at Vantage Hemp. This position will support research of existing and new product lines. The role is predominantly lab-based and located at our production facility in Greeley, CO. Essential Duties and Major Responsibilities: Conduct research studies to further the company's research for existing and new product lines. Conduct processes on a small scale to assist in the development and troubleshooting of large-scale production at Vantage Hemp. The processes may involve distillation, extraction, crystalizing, and winterization. Also, filtration and liquid chromatography. Researches, gathers data; writes, rewrites, and edits research briefs, plans, project proposals, and other written materials; and shares research information, summarizing data collection methods and research findings, with internal and external audiences. Aid in the research into new syntheses and processes for future considerations of new products. Assist in the development of formulations for final product lines. Report all findings in weekly meetings to the executive team. Maintain an up-to-date notebook. Assist with other duties as assigned. Education and Experience needed for the role: Bachelor's degree in Chemistry, Chemical Engineering, or Biochemistry required. Masters degree in a related scientific field preferred. 2+ experience in a lab conducting chemical research and/or development. Knowledge or experience in cannabinoid, or plant related molecule extraction and processing. Prior experience extraction of CBD. Specialized skills needed to be successful: Demonstrate scientific creativity and take initiative. Ability to multi-task and effectively manage timelines. Ability to work in a team environment but have a high level of independence for planning and executing experiments. Well-organized working style with flexibility/adaptability to change. Knowledge of GMP requirements, ICH/FDA Guidelines. Effective oral and written communications. Proficient with Microsoft Office and data analysis/interpretation. Must be 18 years of age or older. Work Hours: The expected hours for this role will be 5 days a week, Monday - Friday, 8 hours a day. Employees' hours vary and are dependent on business needs, and some evenings and weekends may be needed to satisfy the needs of the position. Annual Salary: $57,000 to $65,000 (depending on experience) Benefits: For Full-Time eligible employees, paid time off (3 weeks), 80 hours of sick time, and Employer-paid health and dental coverage for the employee only. Accepting Application Until: 12/31/2025 or until position is filled What types of benefits do we offer? For Full-Time eligible employees, Paid time off (3 weeks - accrued), 80 hours of sick time (prorated from hire), paid company holidays, comprehensive health and dental coverage for the employee, GREAT culture, and a fun place to work. The above statements reflect the principal functions of the occupation described and shall not be construed as a detailed description of all the work requirements that may be inherent in the occupation. **Colorado Residents: In any materials you submit, you may redact or remove age-identifying information such as age, date of birth, or dates of school attendance or graduation. You will not be penalized for redacting or removing this information.

Posting Details Information Position Number T99892 Functional Title Bilingual Research Assistants (English/Spanish) Position Type Temporary Staff Position Eclass ST - SHRA Temp Hourly University Information UNC Greensboro, located in the Piedmont Triad region of North Carolina, is 1 of only 57 doctoral institutions recognized by the Carnegie Foundation for both higher research activity and community engagement. Founded in 1891 and one of the original three UNC System institutions, UNC Greensboro is one of the most diverse universities in the state with 20,000+ students, and 3,000+ faculty and staff members representing 90+ nationalities. With 17 Division I athletic teams, 85 undergraduate degrees in over 125 areas of study, as well as 74 master's and 32 doctoral programs, UNC Greensboro is consistently recognized nationally among the top universities for academic excellence and value, with noted strengths in health and wellness, visual and performing arts, nursing, education, and more. For additional information, please visit uncg.edu and follow UNCG on Facebook, Twitter, and Instagram. Primary Purpose of the Organizational Unit The mission of the Department of Communication Sciences and Disorders is the preparation of diverse students as exemplary, culturally responsive professionals and leaders in the fields of speech-language pathology and audiology. The Department is committed to providing the highest quality academic, research, and clinical training, and to instill in students a desire to make significant contributions to the profession, to the people whom we serve, and to our community. Position Summary * Assist with the administration of language assessments to Latino preschool children (training provided) at preschools in the Greensboro and High Point areas. * Assist with data entry Minimum Qualifications * Experience with children * Experience with data collection and entry * Ability to closely follow lab procedures /protocols * Native-like fluency in both English and Spanish (for Bilingual research assistants) * Excellent verbal and written communication skills. * Valid Driver's License and reliable personal transportation to and from preschools * CITI certification (UNCG Basic Course/Student Researcher Modules/Human Research) or willing to complete certification prior to starting the position Preferred Qualifications Background in communication science disorders, early childhood education, education, or psychology preferred Tenure Status N/A Special Instructions to Applicants Recruitment Range $15/hr Org #-Department Comm Sciences and Disorders - 13001 Job Open Date 09/27/2023 For Best Consideration Date Job Close Date Open Until Filled Yes FTE 0.500 Type of Appointment Temporary Time Limited Duration Number of Months per Year 3 FLSA Non-Exempt ADA Checklist ADA Checklist "R" for Rare (0-30%), "O" for Occasional (30-60%), "F" for Frequent (60-90%), "C" for Constant (90-100%). Physical Effort Hand Movement-Repetitive Motions, Hand Movement-Grasping, Holding, Finger Dexterity, Vision-Skilled Trades, Reading, Writing, Eye-hand coordination, Vision-Color Distinction, Vision-Preparing/Analyzing figures, Vision-Visual inspection, Vision-Measuring/Assembling at distance close to eye, Hearing, Talking, Standing, Sitting, Walking, Lifting-0-30 lbs., Lifting-30-60 lbs., Pushing/Pulling, Climbing-Stairs, Bending, Squatting, Crawling, Reaching Work Environment Driving - Car/Truck, Driving - Standar/Automatic, Inside, Outside Applicant Documents Required Documents * Resume/CV * Cover Letter * List of References Optional Documents Supplemental Questions Required fields are indicated with an asterisk (*). * * Please indicate how you learned of the vacant position for which you are applying: * UNCGjobsearch Website * Greensboro News & Record * Carolina Peacemaker * Other Newspaper * The Chronicle of Higher Education * Inside Higher Ed * Other Professional Journal * NCWorks.gov * UNC System Job Board * Other Online Job Board * Personal Networking * Other * If you selected "Other", please provide the name of the resource here. (Open Ended Question) * * Are you eligible to work in the United States without sponsorship? * Yes * No