Microbiologist jobs in Irvine, CA

We are seeking a highly motivated and detail-oriented Research Technician to join the Structural Quantum Optics ( SQO ) group at Chapman University. The successful candidate will play a central role in establishing a new laboratory, assisting in optical setup and alignment, supporting equipment procurement, and conducting cutting-edge experiments involving entangled photons, Timepix cameras, and single-photon detectors. This position offers hands-on experience with advanced optical instrumentation and the opportunity to contribute to impactful research in a collaborative academic environment Responsibilities Assist in the setup, alignment, and maintenance of optical experiments, including arranging and mounting optics on optical tables. Support the procurement process by identifying, sourcing, and ordering optical components, detectors, and related equipment. Conduct experiments involving spontaneous parametric down-conversion ( SPDC ) sources of entangled photons. Operate, calibrate, and troubleshoot advanced single-photon detection systems, including Timepix cameras and APDs. Maintain laboratory organization, ensuring safe and efficient use of equipment and resources. Collect, analyze, and interpret experimental data; prepare reports, presentations, and contribute to publications. Collaborate with faculty, postdoctoral researchers, and graduate students on experimental design and problem-solving Analyze experimental data using scientific software tools, prepare graphs and summaries, and assist in drafting reports, publications, or presentations. Maintain lab equipment, manage inventory of materials and consumables, and ensure compliance with safety protocols and lab cleanliness standards. Participate in research meetings, present updates, and collaborate with other team members on experimental planning and data interpretation. Required Qualifications Bachelor's degree in physics, Electrical Engineering, Optical Engineering, or a related field. Strong organizational skills and attention to detail Excellent written and oral communication skills Ability to work independently and as part of a research team Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint) Hands-on experience with optical systems, including alignment of lasers, nonlinear crystals, mirrors, lenses, and beam-splitters. Ability to work both independently and collaboratively in a team-oriented research environment. Familiarity with photon detection systems, quantum optics experiments, and imaging systems. Proficiency in scientific data acquisition and analysis (e.g., MATLAB , Python, LabVIEW).

Artech is the 10th Largest IT Staffing Company in the US, according to Staffing Industry Analysts' 2012 annual report. Artech provides technical expertise to fill gaps in clients' immediate skill-sets availability, deliver emerging technology skill-sets, refresh existing skill base, allow for flexibility in project planning and execution phases, and provide budgeting/financial flexibility by offering contingent labor as a variable cost. Job Description • The Quality Assurance Microbiology Laboratory Scientist is responsible for supporting all activities, as well as, performing laboratory testing to insure the materials used and the products manufactured at Company are free of microbiological contamination and in compliance with Good Manufacturing Practice (GMP) and to ensure achievement of Neutrogena's standards for quality. • This individual will comply with Company's policies, procedures, and quality standards as well as safety and environmental regulations. Qualifications: • Minimum Education: A Bachelor s degree in a related scientific field required from an accredited college or university, degree in Microbiology is preferred. Minimum Experience: Two years + of related work experience. • Experience working in a cGMP laboratory setting is required. • Knowledge and experience with current Good Laboratory Practices (GLPs) and current Good Manufacturing Practices (cGMPs) is required. Excellent organization, communication, and problem solving skills is required. Detail oriented, with the ability to work within a team environment as well as thrive in a role as an individual contributor. • This position is located in Los Angeles, California and requires the candidate to work professional work schedule. • Position will support a Tuesday to Saturday or Sunday through Thursday schedule. As the business requires, this candidate will need to cover off shifts for the lab, supporting a 24/7 facility operations. Qualifications Minimum Education: A Bachelor s degree in a related scientific field required from an accredited college or university, degree in Microbiology is preferred. Minimum Experience: Two years + of related work experience. Additional Information Sneha Shrivastava Technical Recruiter (Clinical/Scientific) Artech Information Systems LLC 360 Mt. Kemble Avenue, Suite 2000 | Morristown, NJ 07960 Office: ************ | Fax: ************ Connect with us on - LinkedIn | Facebook | Twitter

Integrated Resources, Inc., is led by a seasoned team with combined decades in the industry. We deliver strategic workforce solutions that help you manage your talent and business more efficiently and effectively. Since launching in 1996, IRI has attracted, assembled and retained key employees who are experts in their fields. This has helped us expand into new sectors and steadily grow. Job Description Under general supervision investigates the growth and characteristics of microscopic organisms such as bacteria, algae and fungi. Designs, conducts and interprets biological experiments to support development programs and identifies biological pathways and agent. Provide biological scientific support to technology and product development. Review scientific and technical summaries, and provides recommendations for potential business applications. Following SOPs and special test designs; analyzes test data and completes required documentation, initiates and manages QA test method improvements, equipment, and process validations. Serve as a team member in the QA Microbiology laboratory; Leads in the implementation of validation and test methods and test correlations. Prepares and executes all protocols and reports for validation work. Will coordinate all validation activities by constant communication with related departments and personnel; oversees and reviews validation area processes and procedures. Responsible for preparing and analyzing timelines and reports to ensure project deliverables arrive on time and within budget. Responsible for providing day-to-day strategic guidance and direction to the Laboratory Technicians regarding validation and process control procedures. Strong Technical writing skills is a mandatory. Clean and maintain laboratory areas and equipment according to procedures. Individual is accustomed with basic and advanced scientific principles and must have laboratory experience. Can follow written direction and maintain a laboratory notebook. Will update SOPs and Work Instructions as directed. Being able to work independently is of the utmost. Has good communication skills and is computer literate. Also responsible for performing more complex laboratory functions and study support. This role will also include documentation improvement, implementation of new equipment upgrades and technology. Sets up, operates and maintains laboratory instruments, monitors experiments, makes observations, calculates and records results, and often develops conclusions. Perform all laboratory processes in accordance with cGMPs, SOPs, TMs safety rules and project/task schedule. Support and coordination of test analysis for the Regulatory Affairs, Manufacturing and R&D departments. Performs QC/equipment maintenance, understands lab safety involving potentially infectious bio-waste and is a team player. Will investigate testing abnormalities and implement non-conformance reporting and corrective action plans. Performs environmental monitoring testing and other special projects by supporting substaining activities in environmentally controlled areas as well as area expansions. Qualifications Minimum a 4 year degree in the sciences (preferential in Microbiology/Engineering/Chemistry/Biochemistry) with 3-5 years' work experience with a proven track record in Equipment Validation and general laboratory techniques within the medical device and/or pharmaceutical industry or master's degree in engineering and 2-3 years of experience in the field or in a related area. Familiar with standard concepts, practices, and procedures within a particular field. Technical writing is a necessary for creation of required reports, specifications, summarizations and other technical documentation. GMP, GLP, GDP, FDA, and OSHA knowledge is required Additional Information Kind Regards, Sasha Sharma Clinical Recruiter Integrated Resources, Inc. IT Life Sciences Allied Healthcare CRO DIRECT # - 732-662-7964

Job Description Certified Group is committed to delivering expert solutions and quality testing our customers can feel confident in - on time, every time - so the world can trust in what it consumes. As a leading North American provider of laboratory testing, regulatory consulting, and certification & audit services, Certified Group includes Food Safety Net Services (FSNS), FSNS Certification & Audit, Certified Laboratories, EAS Consulting Group, and Labstat International Inc. Certified Group provides analytical testing and regulatory guidance services in the food & beverage, dietary supplements & NHP, cosmetics, OTC, personal care, tobacco, nicotine, cannabis, and hemp industries. We have embarked on an important journey to unify and strengthen our culture by living these core values: Start with the Customer, Drive to Deliver, Commit to Safety and Quality, and Believe in the Team - including believing in you. We are currently looking for a Microbiologist to join our growing team! JOB SUMMARY The function of this job is to perform advanced analytical and microbiological testing of food products, ingredients, and environmentals. The position consistently exercises independent judgment and discretion in performing the application and evaluation of approved microbiological techniques and methodologies used in analytical testing, and the interpretation of test results. This role has training and supervisory responsibilities as needed. ESSENTIAL RESPONSIBILITIES Accurately perform and read test results and notify Laboratory Management of deviations Prepare and analyze samples for indicator organisms, pathogens, and chemistries Apply aseptic/microbiological techniques in daily workload Apply independent judgement in the interpretation of qualitative test results Conduct additional testing as needed based upon independent review of test results Accurately perform final determination of special micros and complete final results disposition Communicate results including pathogenic confirmations and maintain a positive relationship with clients Report inventory and expendable supplies/materials needed for testing requirements Provide routine preventive maintenance by daily cleaning, sanitizing, trash disposal, and equipment quality control Assist in quality control duties to by taking incubator temperatures, inoculating control organisms, running media controls, etc. Assist with training and research assignments including troubleshooting Independently pursue an assigned series of processes, procedures, or techniques in accordance with FSNS policies/procedures and customer requirements Assisting in developing and revising Standard Operating Procedures (SOPs) Maintain a high degree of technical competence by reading scientific journals, attending professional workshops, and being aware of food industry issues and trends Perform all activities in a neat, safe, hygienic, and efficient manner Share information in an open and timely manner Assist with managing priorities and schedule Responsible for the safety of oneself and others working within their area Responsible for the completion of required training Travel is required and at the discretion of management OTHER DUTIES Perform other duties as assigned As needed from time to time, assist in performing Login Technician, Media Technician, and/or Micro Technician. If assigned, conduct responsibilities of Branch Safety Coordinator outlined in the corporate safety manual and report to the Corporate Safety Officer for assigned duties SUPERVISORY RESPONSIBILITIES This job has no regularly assigned supervisory responsibilities, although the position is expected to train others, and step in to perform supervisory responsibilities when the Sr. Microbiologist, Lead or the Supervisor is not available. MINIMUM QUALIFICATIONS Bachelor's degree in Life Science or related field, microbiology preferred Two or more years of experience in a commercial food-testing or analytical laboratory Or equivalent combination of education and experience Working knowledge of aseptic sampling technique, automated lab equipment, and acceptable methods and procedures Familiar with GLP, OSHA guidelines, FDA, BAM, APHA, ISO, and USP methods and procedures Broad knowledge of concepts, practices, and procedures of a food testing laboratory Ability to travel when necessary KNOWLEDGE, SKILLS, and ABILITIES To perform the job successfully, an individual should demonstrate the following: Computer - Proficient in standard business office software, LIMS, and internet search tools. Customer Service - Responds promptly to customer needs; Responds to requests for service and assistance; Meets commitments. Verbal & Written Communication; Language Skills - Clarity of speech, remaining calm and focused, being polite and making effective presentations to diverse groups. Edits work for correct data, spelling, and grammar. Ability to read and comprehend simple instructions, short correspondence, and memos. Mathematical Skills - Ability to add, subtract, multiply, and divide in all units of measure, using whole numbers, common fractions, and decimals; Ability to perform financial calculations, compute rate, ratio, and percent and to draw and interpret bar graphs. Analytical, Problem Solving, & Organizational Skills - Gathers and analyzes information skillfully and can efficiently execute on plans/ideas. Ability to deal with problems involving a few concrete variables in standardized situations. Interprets data and test results. Independent Judgement and Discretion - Proficient and confident in exercising independent judgement and discretion on a consistent basis throughout the day in performing the testing, analytical and interpretive responsibilities of the position. 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. FSNS complies with its reasonable accommodation obligations under the Americans with Disabilities Act and state law. Regularly required to stand, sit, walk, use hands and arms, talk and hear Lift up to 25 pounds Color vision and depth perception 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. Potential exposure to odors, fumes, airborne particles, hazardous chemicals, and microbiological pathogens Noise level varies from quiet to loud Temperature varies from hot to cold Interactive and fast-paced team oriented tasks Safety: Required to wear appropriate protective clothing Required to use appropriate protective equipment Responsible for the safety of oneself and others working within their area PROFICIENCY REQUIREMENTS Employees in this role will be evaluated after 90 calendar days from date of hire and annually thereafter based on the following proficiencies: In addition to the responsibilities of this position, maintain competency in duties performed by technicians in other departments (Log-In, Media, Main) to provide assistance when needed Exercise of sound independent judgment and discretion Knowledge of all qualitative, quantitative testing, and confirmations performed Resource for all technicians in Main Lab Proficient in the passing and first approval process and may complete second approvals Excellent aseptic technique and use of the biological hood Understand client specifications Ability to assume the responsibilities and make decisions of the Sr. Microbiologist, Lead, or Supervisor, when they are not available Ensure daily, weekly, and monthly sanitation and QC are complete Help resolve technical issues with machines Proficiency in testing for all path lab analyses on A2LA Scope ( Versed in GLP, FDA, USDA, AOAC, and other method reference sources Manage workload and ensure TAT is met by delegation of work to self and others Assist Technical Manager, as needed All Certified Group employees must be proficient in the following: Ability to multitask and quickly move from one task to the next Ability to complete tasks with accuracy General knowledge of all FSNS safety protocols & general OSHA laboratory safety guidelines Working knowledge of ISO 17025 Quality procedures general to their primary job and area of responsibility Ability to perform laboratory opening and closing procedures Benefits: Progressive 401k Retirement Savings Plan Employer Paid Short- Term and Long-Term Disability, and Life Insurance Group Medical Tuition Reimbursement Flexible Spending Accounts Dental Paid Holidays and Time Off Many positions which qualify for the company bonus program Certified Group values diversity in its workforce. The company is firmly committed to a policy of Equal Opportunity and will administer its policies in a manner that treats each employee and applicant for employment on the basis of merit. Certified Group will take affirmative action to seek out qualified applicants without regard to race, color, religion, sex, national origin, age, handicap, or veteran status. Monday through Friday, 8:00AM to 5:00PM

Hi, Greetings!!! I am Sree from Infinite Computing Systems . I am looking for a for Sterilization Microbiologist for a my direct client that is among the founders of the scientific practice of pharmacy, expanding its business to meet rising global health needs by championing new areas of medical research. And they holds the No. 1 position in rapid testing for cardiometabolic disease, infectious disease and in toxicology. This is an Onsite position at Sylmar, CA. If you are interested let me know the best number and time to reach you so that we can have a quick discussion and take it further. You can also reach me at ************. Job Description Job Title: Sterilization Microbiologist Duration: 06/28/2021 to 12/31/2021 Location: Sylmar CA (onsite) Performs sterilization validation for new and existing products utilizing Ethylene Oxide and Radiation sterilization methods. Support R&D for sterilization validation of new products and changes to existing products. 1. Responsible for compliance with applicable Corporate and Divisional Policies and procedures. 2. Conduct sterilization qualification for new products and/or changes to existing products. 3. Performs sterilization validation for radiation sterilized products including dose setting and quarterly dose audits. 4. Performs sterilization validation for ethylene oxide sterilized products including new product qualification, annual revalidations, residual EO studies, and D-value studies. 5. Provides product development teams sterilization Subject Matter Expert support 6. Assist in Supplier Quality audits of contract sterilization facilities and third party manufacturers. 7. Conducts dose audit failure investigations. 8. Conducts Ethylene Oxide Biological indicator sterility positive investigation. Understands business environment and relates extensive knowledge of internal and external technological activities to trends. Interfaces with senior management on significant matters, often requiring the coordination of activity across organizational units. Participates in the development of other technical contributors by facilitating training and providing feedback and guidance. May lead a project team. Provides technical leadership to business units. Acts as a mentor to less-experienced staff and may provide work direction or supervise other technical employees. Exercises judgment independently. Plans and organizes project assignments of substantial variety and complexity. Initiates or maintains schedule for projects and project milestones. Establishes priorities of individual or project assignments. Selects methods and techniques to lead a project to completion. Erroneous decisions or recommendations would typically result in failure to achieve major organizational objectives Qualifications Bachelor's degree plus 9+ years of related work experience with a complete understanding of specified functional area, or an equivalent combination of education and work experience. Requires 5 to 10 years direct experience with Radiation and/or Ethylene Oxide sterilization. (Advanced degree preferred.)) Comprehensive knowledge of a Radiation and or Ethylene Oxide sterilization. Uses in-depth knowledge of business unit functions and cross group dependencies/ relationships. Is recognized as an expert in work group and across functions. Will perform this job in a quality system environment. Failure to adequately perform tasks can result in noncompliance with governmental regulations. Works on complex problems where analysis of situations or data requires an in-depth evaluation of various factors. Exercises judgment within broadly defined practices and policies in selecting methods, techniques and evaluation criteria for obtaining results. Has broad knowledge of various technical alternatives and their potential impact on the business Additional Information Interested resource please share resume at snair@infiite-usa. com

Certified Group is a leading North American provider of laboratory testing and audit and certification services. The Certified Group of companies includes Food Safety Net Services (FSNS), Certified Laboratories, EAS Consulting Group, Labstat International Inc., Advanced Botanical Consulting & Testing (ABC Testing Inc.), Microconsult Inc. and Micro Quality Labs Inc. The Certified Group provides analytical testing and regulatory guidance services in the food & beverage, dietary supplements & NHP, cosmetics, OTC, personal care, tobacco, cannabis, nicotine and hemp industries. We are currently looking for a Microbiologist to join our team! ESSENTIAL RESPONSIBILITIES Study the growth, characteristics and effects of bacteria and other microorganisms to better understand their relation to human, plant and animal health. Perform sterility testing Perform API strips & troubleshoot issues and concerns regarding cross-contamination Adapt and understand the procedures from CTFA, AOAC and others as needed. Perform Total Plate Counts, Enrichments, Preservative Effectiveness Testing, raw material testing, bulk testing, water testing and other tests. Perform other duties as assigned. MINIMUM QUALIFICATIONS Must have a B.S. in Microbiology At minimum, 2 years of microbiological testing experience in the cosmetic, nutritional or pharmaceutical industries. Knowledge of current CTFA/PCPC, AOAC and other industry standard methods and procedures. Understanding of pharmaceutical, cosmetic and nutritional microbiology. Understanding and knowledge of the European, United States, Japanese and other Pharmacopeias. Experience performing microbial testing on pharmaceutical, cosmetic and nutritional raw materials, water samples, bulk & finished products. Example of these tests are: Total Plate Count (TPC), Yeast & Mold, Enrichments and Preservative Effectiveness Testing (PET). Computer literate. Be able to work with Microsoft programs, search engines, basic spreadsheets, etc. Able to handle multiple tasks and work in a fast paced environment. Able to adapt to changes to improve company process. May assist in overseeing work performed by Microbiology Technician. Benefits : Progressive 401k Retirement Savings Plan Employer Paid Short- Term and Long-Term Disability, and Life Insurance Group Medical Tuition Reimbursement Flexible Spending Accounts Dental Paid Holidays and Time Off Many positions which qualify for the company bonus program Certified Group values diversity in its workforce. The company is firmly committed to a policy of Equal Opportunity and will administer its policies in a manner that treats each employee and applicant for employment on the basis of merit. Certified Group will take affirmative action to seek out qualified applicants without regard to race, color, religion, sex, national origin, age, handicap, or veteran status.

Job Description Clinical Laboratory Scientist (CLS) / Clinical Microbiologist Scientist About Us At Primex Clinical Laboratories, we're dedicated to enhancing health with precision and passion. Since 1996, our presence in clinical diagnostics has been unwavering, serving clients across Central and Southern California, Nevada, and American Samoa. We pride ourselves on delivering personalized service and high-quality testing with quick, accurate results. Position Summary We are seeking a detail-oriented and experienced Clinical Laboratory Scientist (CLS)/Clinical Microbiologist Scientist to join our laboratory team. The role involves performing microbiological and clinical laboratory testing to support accurate diagnosis, treatment, and monitoring of patient health. The ideal candidate is skilled in microbiology techniques, follows strict quality and safety protocols, and thrives in a collaborative, fast-paced clinical environment. Key Responsibilities Perform routine and specialized microbiology testing (culture, identification, and susceptibility testing of microorganisms). Process and analyze patient specimens in compliance with laboratory procedures and regulatory requirements (CLIA, CAP, and state guidelines). Operate and maintain laboratory instruments and equipment. Interpret, record, and report laboratory results accurately in the Laboratory Information System (LIS). Participate in quality control, proficiency testing, and quality improvement activities. Follow biosafety and infection control procedures to ensure a safe work environment. Collaborate with pathologists, physicians, and other laboratory staff to ensure timely and accurate results. Stay current with advances in microbiology and laboratory testing practices. Qualifications Required: Valid Clinical Laboratory Scientist (CLS) license or Clinical Microbiologist Scientist License. Bachelor's degree in Medical Technology, Microbiology, Biology, or related field. Hands-on experience in microbiology testing and general clinical laboratory practices. Preferred: At least 2 years of experience in a clinical microbiology laboratory. Familiarity with automated microbiology systems and molecular diagnostic techniques. Strong problem-solving, organizational, and communication skills. Work Environment & Physical Requirements Laboratory setting with exposure to biohazardous materials. Compliance with PPE requirements. Demonstrate a cooperative attitude towards working harmoniously with colleagues. Schedule & Location 6am - 2:30 pm, Full-time, Wednesday to Sunday, or; 6am - 2:30 pm, Full time, 4 weekdays plus rotating weekends' or; 6am - 3:30 pm, Part time, 3-4 day per week, rotating weekends and vacation, holiday and after hours coverage as necessary. This position is an on-site at Primex Clinical Laboratories, Inc. 16742 Stagg St. #120 Van Nuys, CA 91406. Primex Clinical Laboratories is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, gender identity or expression, sexual orientation, national origin, age, disability, veteran status, or any other legally protected status.

How will you make an impact? This microbiologist role will have a strong background in performing method development, method validation, method transfer activities as well as routine testing of raw materials, in-process testing and finished product. This exciting role will support microbiological activities for the Glaukos organization, which includes R&D as well as commercial manufacturing. The candidate must have experience in cGMPs, regulatory body requirements and FDA compliance and must be proficient in microbiological testing per USP/EP/JP. The candidate must have an understanding of aseptic processes and manufacturing. What You'll Do: Develop and implement microbiological strategies and procedures to ensure compliance with industry standards and regulations Perform method development, feasibility and validation of raw materials, in-process and final product. Conduct routine microbiological testing and analysis of samples, ensuring accuracy and reliability of results. Perform routine and stability testing of GLP and GMP supplies Write and revise SOP's, validation protocols/reports Perform testing as needed to generate data for validation and special projects. Make recommendations and validate new laboratory equipment (e.g., Installation Qualification, Operational Qualification (IQOQ), and Performance Qualification (PQ) Maintain accurate and up-to-date documentation of all microbiological activities, including test results, procedures, and reports Review and interpret test results, prepare reports, and communicate findings to relevant stakeholders Identify and implement improvements to existing microbiological processes, methods, and techniques to enhance efficiency and productivity Collaborate with cross-functional teams, such as quality assurance, research and development, and production, to support product development and continuous improvement initiatives Stay updated with the latest advancements and trends in the field of microbiology and recommend and implement new technologies and methodologies as appropriate Ensure compliance with relevant regulatory requirements and standards, such as Good Manufacturing Practices (GMP), Hazard Analysis and Critical Control Points (HACCP), and ISO standards How will you get here? Bachelor's degree in Microbiology, Biology or related scientific field Minimum 8 years of related pharmaceutical experience in a cGMP environment Proficiency in microbiological techniques such as aseptic testing, microbial monitoring, gram staining, and plating Proficiency in testing according to AAMI/ISO/USP Standards Knowledge and control of laboratory equipment including calibration and maintenance Ability to understand and perform all required tasks by adhering to company Standard Operating Procedures and all current Good Manufacturing Practices Understanding of quality systems including change control, deviations and CAPAs; support investigations as needed Ability to handle multiple tasks concurrently and complete tasks in a timely manner Strong written and verbal language skills to effectively read and write SOP's and related labreports and effective communication skills to present data with personnel at all levels in the organization Excellent teamwork skills, organizational skills, and strong attention to detail Knowledgeable in regulatory requirements and industry standards related to microbiology Proficient in using microbiological testing equipment and software; Knowledge and proficiency in computer software (e.g. Microsoft Office programs) Attention to detail and high level of accuracy in performing microbiological tests and analysis and excellent analytical and problem-solving abilities to interpret test results, troubleshoot issues, and recommend solutions Ability to work collaboratively in cross-functional teams and adapt to changing priorities and deadlines Strong organizational and time management skills to prioritize tasks and meet project timelines Ability to lift 25 lbs. Ability to stand or sit 8 or more hours a day Work in a sterile environment wearing appropriate gowning and protective equipment #GKOSUS

How will you make an impact? This microbiologist role will have a strong background in performing method development, method validation, method transfer activities as well as routine testing of raw materials, in-process testing and finished product. This exciting role will support microbiological activities for the Glaukos organization, which includes R&D as well as commercial manufacturing. The candidate must have experience in cGMPs, regulatory body requirements and FDA compliance and must be proficient in microbiological testing per USP/EP/JP. The candidate must have an understanding of aseptic processes and manufacturing. What You'll Do: Develop and implement microbiological strategies and procedures to ensure compliance with industry standards and regulations Perform method development, feasibility and validation of raw materials, in-process and final product. Conduct routine microbiological testing and analysis of samples, ensuring accuracy and reliability of results. Perform routine and stability testing of GLP and GMP supplies Write and revise SOP's, validation protocols/reports Perform testing as needed to generate data for validation and special projects. Make recommendations and validate new laboratory equipment (e.g., Installation Qualification, Operational Qualification (IQOQ), and Performance Qualification (PQ) Maintain accurate and up-to-date documentation of all microbiological activities, including test results, procedures, and reports Review and interpret test results, prepare reports, and communicate findings to relevant stakeholders Identify and implement improvements to existing microbiological processes, methods, and techniques to enhance efficiency and productivity Collaborate with cross-functional teams, such as quality assurance, research and development, and production, to support product development and continuous improvement initiatives Stay updated with the latest advancements and trends in the field of microbiology and recommend and implement new technologies and methodologies as appropriate Ensure compliance with relevant regulatory requirements and standards, such as Good Manufacturing Practices (GMP), Hazard Analysis and Critical Control Points (HACCP), and ISO standards How will you get here? Bachelor's degree in Microbiology, Biology or related scientific field Minimum 8 years of related pharmaceutical experience in a cGMP environment Proficiency in microbiological techniques such as aseptic testing, microbial monitoring, gram staining, and plating Proficiency in testing according to AAMI/ISO/USP Standards Knowledge and control of laboratory equipment including calibration and maintenance Ability to understand and perform all required tasks by adhering to company Standard Operating Procedures and all current Good Manufacturing Practices Understanding of quality systems including change control, deviations and CAPAs; support investigations as needed Ability to handle multiple tasks concurrently and complete tasks in a timely manner Strong written and verbal language skills to effectively read and write SOP's and related labreports and effective communication skills to present data with personnel at all levels in the organization Excellent teamwork skills, organizational skills, and strong attention to detail Knowledgeable in regulatory requirements and industry standards related to microbiology Proficient in using microbiological testing equipment and software; Knowledge and proficiency in computer software (e.g. Microsoft Office programs) Attention to detail and high level of accuracy in performing microbiological tests and analysis and excellent analytical and problem-solving abilities to interpret test results, troubleshoot issues, and recommend solutions Ability to work collaboratively in cross-functional teams and adapt to changing priorities and deadlines Strong organizational and time management skills to prioritize tasks and meet project timelines Ability to lift 25 lbs. Ability to stand or sit 8 or more hours a day Work in a sterile environment wearing appropriate gowning and protective equipment #GKOSUS

Lead all laboratory activities and functions within the Microbiology Laboratory. Main responsibility consists of the testing of the routine external PCDs (Product Challenge Devices) used for the in-house steam and ethylene oxide sterilization processes, including the generation of any applicable test method and other related documents needed for the laboratory and any associated testing, IQ/OQ of all laboratory equipment, and routine monitoring of all temperature-controlled incubators and refrigerator. Take a proactive role in supporting the manufacturing team, provide internal customer support, and build a high level of trust with internal customers and MV personnel. Support any non-conformance investigation activities. Job duties: + Responsible for routine finished product sterility testing of steam and ethylene oxide external PCDs, including the tracking status of all testing within the laboratory. + Must interpret and apply specifications and test procedures when carrying out monitoring and testing responsibilities. + Responsible for the general cleanliness and appearance of the Micro Lab by keeping laboratory equipment, supplies, and overall environment in good operational status. + May prepare media reagents, testing materials, and equipment as required. + Responsible for ordering and maintaining materials, and supplies. + Record data in controlled company forms, validated spreadsheets, and build records. + May be required to work on special projects such as investigations and non-routine testing. + Maintain neat and legible records. + Follow cGMPs, GLPs, SOPs, USP, and FDA guidelines in all appropriate functions and notify management of any observed discrepancies in laboratory. + Comply with applicable Laws and Regulations, adhere to Quality Management System processes and requirements as well as demonstrate Ethics and Integrity in all matters and at all levels throughout the organization. + Perform additional duties as assigned. **Auto req ID:** 13064BR **Location MV:** Aliso Viejo, California, USA **Department Name:** 524-New Product Quality **Qualifications:** 1. HS diploma or equivalent. 2. Minimum five (5) years of related work experience. 3. Strong computer skills including MS Word, Excel, Teams, Outlook, etc. 4. Good written and verbal communication skills. 5. Ability to read, write, and speak in English. 6. Good laboratory or manufacturing practices and ability to follow required safety procedures. 7. Strong background and understanding of aseptic laboratory practices. 8. Good laboratory or manufacturing practices and ability to follow required safety procedures. 9. Experience with reading and preparing technical documentation. 10. Flexible to work nights and weekends, if necessary. **Desired Qualifications** 1. Ability to analyze, investigate, and help solve technical issues involving steam and/or ethylene oxide sterilization and related equipment. 2. Ability to work independently and work efficiently in a fast-paced environment with shifting priorities. 3. Excellent time management, prioritization, and organizational skills. 4. Ability to promote effective working relationships at all levels, create a positive work environment, and collaborate with others in a team-based environment. 5. Excellent attention to detail. 6. Experience with steam or ethylene oxide sterilizers. 7. Related experience with working and handling biological indicators. 8. Experience in the medical device industry. **External-Facing Title:** Microbiology Lab Technician **Posting Country:** US - United States **Salary Range:** $27.00/hour Financial compensation packages may be higher or lower than what is listed, and will ultimately depend on factors including relevant experience, internal equity, skillset, knowledge, geography, education, business needs and market demand. We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, ethnicity, disability, religion, national origin, gender, gender identity, gender expression, marital status, sexual orientation, age, protected veteran status, or any other characteristic protected by law.

Job DescriptionBioPhase Solutions specializes in recruiting top talented professionals for Southern California's Scientific community. We are currently looking for a QC Microbiologist I to work for a leading Orange County area biotechnology company. Pay Rate: $29-32/hour Summary:Perform microbiological testing of raw materials, intermediates, API, drug product release and stability samples, as well as collection and testing of environmental monitoring samples, in accordance with cGMP requirements, company policies and procedures as directed by laboratory management. Responsibilities Responsibilities: Perform routine microbiological laboratory analysis, such as Environmental Monitoring, Bioburden, Microbial Limits (preparatory & screening), Sterility, Endotoxin (Gel-Clot & Kinetic methods), operate autoclave, and prepare media in accordance with Customer, schedule and cGMP requirements. Read and understand test methodologies, study protocols, and Standard Operating Procedures in order to review or execute testing in compliance with necessary policies and procedures. Record/review data in controlled notebooks, data sheets, and electronic systems (i.e. LIMS, etc.) in accordance with cGMP requirements. Work on routine tasks where analysis of situations or data requires review and evaluation of limited factors, limited judgment is required in resolving problems and making routine recommendations. Exercise judgment within defined practices and policies in selecting methods, techniques, and evaluation criteria for obtaining results. Notify supervisor of any discrepancy in laboratory testing or general laboratory operations. In case of any observed discrepancies, initiate and follow through with the required quality exception documentation as needed. Assume ownership of assigned quality documentation, such as exceptions, change controls, and CAPAs, ensuring that documentation is initiated and closed on time, required actions are thorough and meet procedural requirements as well as customer needs. Obtain and maintain aseptic gowning qualification. Recommend equipment, facility and process improvements to your supervisor. Maintain clear, accurate and traceable manufacturing records to ensure compliance with Good Documentation Practices (GDP) Maintain laboratory and workspace cleanliness by adhering to the 5S method of organization. Abide by safe work practices and adhere to general safety rules, performing all duties in a safe manner and never placing yourself or those around you in an unsafe condition. Report all unsafe conditions to your supervisor. This list of duties and responsibilities is not all inclusive and may be expanded to include other duties and responsibilities, as management may deem necessary. Qualifications: Minimum of 1-2+ years industry experience. Bachelor's degree or equivalent in scientific discipline required. Knowledge of cGMP regulations, and FDA and ICH guidelines as they pertain to aseptic manufacturing operations. Knowledge of aseptic manufacturing regulations, aseptic technique, clean room behaviors, and environmental monitoring operations. Knowledge of USP, Pharm. Eur. and other compendial methods and procedures. Knowledge of microbiological practices, procedures, and common analyses, such as Environmental Monitoring, Bioburden, Microbial Limits (preparatory & screening), Sterility, Endotoxin (GelClot & Kinetic Chromogenic methods), validation - Inhibition/Enhancement Sterility Test Method Validation (Bacteriostasis/Fungistasis), and Preservative Efficacy Testing. Knowledge in the use of LIMS and electronic documentation systems (i.e. MasterControl). Please send resumes to *********************** and visit our website at ******************* for additional job opportunities!!!

THIS ANNOUNCEMENT IS BEING REPOSTED TO REOPEN THE FILING PERIOD TO ALLOW ADDITIONAL APPLICATION FILING AND UPDATE BULLETIN LANGUAGE. EXAM NUMBER: PH4999C TYPE OF RECRUITMENT We welcome applications from anyone! FIRST DAY OF FILING: The application filing period will begin on Monday, November 3, 2025 at 8:30 a.m. (PT) - Continuous. We will keep accepting applications until the position is filled. The application window may close unexpectedly once we have enough qualified candidates. CHECK OUT OUR OUTSTANDING BENEFITS! We offer one of the strongest public-sector benefits packages in the country, including diverse healthcare choices, and strong retirement plans. For more information about the outstanding benefits offered by Los Angeles County, please visit us here: ********************************* ABOUT THIS POSITION: We are pursuing qualified candidates to fill the Public Health Microbiologist I positions within the Department of Public Health. The position performs a variety of standardized public health laboratory tests within a specialized area (such as bacteriology, virology, serology, or parasitology) or across specialty lines. For information about the specific classification standards for this position, please visit the following link: Public Health Microbiologist I.What will I do as a Public Health Microbiologist I? * Conducts specialized parasitology examinations to identify ova, worms, and protozoa present in fecal specimens. * Performs microbiological examinations for the detection and identification of viral agents utilizing live host systems such as tissue cultures, embryonated eggs, and suckling and adult white mice; examines brain material from various animals for suspected rabies. * Isolates and identifies fungi of medical significance by correlating information derived from stained smears, wet mounts, biochemical patterns, and colony morphology. * Makes microbiological examinations of body fluids, discharges, secretions and blood specimens to determine the presence of mycobacteria, gonorrhea, typhoid, salmonella, shigella, and related organisms, and of foods suspected of causing food poisoning. * Performs serological laboratory examinations including agglutination, precipitation, absorption, immunofluorescence and complement fixation tests in connection with the detection and control of syphilis and other diseases. * Conducts specific biochemical tests on blood, blood plasma, urine and other body fluids to determine the presence and quantity of specific metabolic substances, and performs such hematological procedures as electrophoresis, complete blood counts, blood sedimentation rates, hemoglobin determinations, and hematocrits. * Calibrates laboratory instruments following prescribed methods and performs other quality control procedures to assure the operational accuracy of equipment and test reproducibility; performs first-line maintenance on such equipment. * Gives bench-level instruction on the detailed aspects of assignments to approved trainees, newly hired microbiologists, and professional personnel from medical laboratories in the community who have been referred or seek assistance in the proper conduct of test procedures. REQUIREMENTS TO QUALIFY: A current Public Health Microbiologist's certificate* issued by the California State Department of Public Health. LICENSE: A valid California Class C Driver License or the ability to utilize an alternative method of transportation to perform job-related essential functions may be required. PHYSICAL CLASS: 2 - Light: This class includes administrative and clerical positions requiring light physical effort that may include occasional light lifting to a 10 pound limit and some bending, stopping, or squatting. Considerable ambulation may be involved. SPECIAL REQUIREMENT INFORMATION: * In order to receive credit for any required certifications, you must attach a legible copy of the certificate/letter with your application online at the time of filing or within fifteen (15) calendar days from application submission to *********************** For information on how to obtain the letter/certificate from the California State Department of Public Health verifying eligibility to work as a public health microbiologist, click on the link below: ******************************************************************* We do not accept password-protected documents. Ensure documents are unlocked before attaching to your application or sending to the exam analyst. DESIRABLE QUALIFICATIONS: The experience listed below must be work experience beyond the Minimum Requirements. * Experience utilizing software programs such as Microsoft Office (word, excel, power point or access) to create documents, reports, databases, flow charts, etc. * Experience in a research, clinical, or public health laboratory. * Experience with laboratory techniques including microscopy, gel electrophoresis, nucleic acid extraction, polymerase chain reaction (PCR), DNA sequencing, etc. * Experience using diagnostic testing methodologies to include limitations of testing, reference methods, appropriate test utilization, and test interpretation. * Experience using diagnostic testing methodologies for bacterial serotyping, water, and dairy sample testing. EXAMINATION CONTENT This assessment type will evaluate the education and experience you list on a questionnaire and assign a score based on a standardized scoring system. This part of the assessment is worth 100% of your total score and assesses: Requirements and Desirable Qualifications. Candidates must meet the requirements to qualify and must achieve a passing score of 70% or higher on the examination in order to be added on the Eligible List. Passing this examination and being added to the Eligible List does not guarantee an offer of employment. ELIGIBILITY & VACANCY INFORMATION Candidates who passed the assessment are placed on the Eligible List in the order of their score group for a period of twelve (12) months following the date of eligibility. The Eligible List resulting from this examination will be used to fill vacancies in the Department of Public Health as they occur. Applications will be processed as they are received and added to the Eligible List accordingly. AVAILABLE SHIFT Any, including evenings, nights, weekends and holidays. APPLICATION AND FILING INFORMATION HOW TO APPLY: We only accept applications filed online. Applications submitted by U.S. mail, fax, or in person are not accepted. Apply online by clicking on the "Apply" green button at the top right of this posting. This website can also be used to get application status updates. Please fill out the application completely. Provide relevant job experience including employer's name and address, job title, beginning and ending dates, number of hours worked per week, and description of work performed. If the application and/or Supplemental Questionnaire is/are incomplete, the application will be REJECTED. IMPORTANT NOTES: We may verify information included in the application at any point during the examination and hiring process, including after an appointment has been made. Falsification of information could result in refusal of application or rescission of appointment. Copying verbiage from the Requirements or class specification as your work experience will not be sufficient to demonstrate meeting the requirements. Doing so may result in an incomplete application and may lead to disqualification. We will send notifications to the email address provided on the application, so it is important that you provide a valid email address. If you choose to unsubscribe or opt out from receiving our emails, it is possible to view notices by logging into governmentjobs.com and checking the profile inbox. It is every applicant's responsibility to take steps to view correspondence, and we will not consider claims of missing notices to be a valid reason for extensions. Register the below domains as approved senders to prevent email notifications from being filtered as spam/ junk mail. * *********************** * *********************** New email addresses need to be verified. This only needs to be done once per email address and can be done at any time by logging in to governmentjobs.com and following the prompts. This is to enhance the security of the online application and to prevent incorrectly entered email addresses. COMPUTER AND INTERNET ACCESS AT PUBLIC LIBRARIES: For candidates who may not have regular access to a computer or the internet, applications can be completed on computers at public libraries throughout Los Angeles County. SOCIAL SECURITY NUMBER: Please include your Social Security Number for record control purposes in the format XXX-XX-XXXX. Federal law requires that all employed persons have a Social Security Number. NO SHARING OF USER ID AND PASSWORD: All applicants must file their application online using their OWN user ID and password. Using a family member or friend's user ID and password may erase a candidate's original application record. VETERAN'S CREDIT: If you are a veteran, you may be eligible for veteran's credit, which is an additional 10% of the total points added to a passing score. We will need a copy of your form DD214 to review, so please include that with your application or email it to *********************** as soon as possible so, if you are eligible for veteran's credit, we can include it before the list is available. ANTI-RACISM, DIVERSITY, AND INCLUSION (ARDI): The County of Los Angeles recognizes and affirms that all people are created equal and are entitled to all rights afforded by the Constitution of the United States. We are committed to promoting Anti- racism, Diversity, and Inclusion efforts to address the in equalities and disparities amongst race. We support the ARDI Strategic Plan and its goals by improving equality, diversity, and inclusion in recruitment, selection, and employment practices. Department Contact Name: Exam Analyst Department Contact Phone: ************** Department Contact E-mail: *********************** California Relay Services Phone: ************** ADA Coordinator Phone: ************** Teletype Phone: ************** Alternate Teletype Phone: **************

The posted pay scale represents the range the Company reasonably expects to pay candidates for this position. The actual wage for this position may depend on factors such as experience and education, specific skills and abilities, alignment with similar internal candidates, marketplace factors, an applicable collective bargaining agreement, and Company business practices. Under limited supervision, collects specimens and performs clinical laboratory tests to obtain data for use in the diagnosis and treatment of disease in accordance with accepted standards and practices. Inputs data and retrieves reports from computer as necessary. In the absence of supervisor, may function as lead shift CLS, resolving technical and operational issues in conjunction with administration or house supervisor. Additionally, may function as bench supervisor in absence of technical supervisor, creating or reviewing QC and/or QA documentation as needed and delegated.QUALIFICATIONS: CA license as a Clinical Laboratory Scientist Bachelor's Degree in Biology or Chemistry. Minimum 6 years' experience in relevant areas of the lab, including transfusion services. Experience with state and federal regulations including CA, CAP, and Cal/OSHA. Lead CLS experience in one or more laboratory departments preferred. Benefits : Medical, dental and vision coverage is provided for all full time and part time employees* Medical is 100% employer paid including dependents* Employee Assistance Program Basic Life and AD&D 401k plan with company match Generous PTO plan* Pet Insurance Discount Program* Employee Discount Program**Per diem staff ineligible

The posted pay scale represents the range the Company reasonably expects to pay candidates for this position. The actual wage for this position may depend on factors such as experience and education, specific skills and abilities, alignment with similar internal candidates, marketplace factors, an applicable collective bargaining agreement, and Company business practices. Under limited supervision, collects specimens and performs clinical laboratory tests to obtain data for use in the diagnosis and treatment of disease in accordance with accepted standards and practices. Inputs data and retrieves reports from computer as necessary. In the absence of supervisor, may function as lead shift CLS, resolving technical and operational issues in conjunction with administration or house supervisor. Additionally, may function as bench supervisor in absence of technical supervisor, creating or reviewing QC and/or QA documentation as needed and delegated.QUALIFICATIONS: CA license as a Clinical Laboratory Scientist Bachelor's Degree in Biology or Chemistry. Minimum 6 years' experience in relevant areas of the lab, including transfusion services. Experience with state and federal regulations including CA, CAP, and Cal/OSHA. Lead CLS experience in one or more laboratory departments preferred. Benefits : Medical, dental and vision coverage is provided for all full time and part time employees* Medical is 100% employer paid including dependents* Employee Assistance Program Basic Life and AD&D 401k plan with company match Generous PTO plan* Pet Insurance Discount Program* Employee Discount Program**Per diem staff ineligible

Caltech is a world-renowned science and engineering institute that marshals some of the world's brightest minds and most innovative tools to address fundamental scientific questions. We thrive on finding and cultivating talented people who are passionate about what they do. Join us and be a part of the diverse Caltech community. Job Summary Provide technical assistance to a group of professors and their graduate and undergraduate students and postdoctoral scholars involved in engineering research on materials and structures; materials include polymers, metals, and composites. Work involves design and set-up of new and existing research facilities, including the knowledge to operate laboratory equipment for research and train new students. This would include hydraulic, optical, electronic, piezo, 3D printing, X-ray instrumentation and composites manufacturing. Training of students and postdoctoral scholars to adopt safe research practices is also included in this job. Essential Job Duties Independently operate and maintain equipment related to solid and structural mechanics research. Train and assist students and postdoctoral scholars in the safe operation of this equipment and document operating procedures when necessary. Learn from engineering sketches, technical documentations, and oral instructions, circuits and devices for measurements and fixtures for mechanical testing and repair mechanical instruments. Coordinate with external companies for regular maintenance, upgrades, and emergency repairs. Order supplies and provide technical support in optics, photography, 3D printing, X-ray optics, and data acquisition. Perform experiments for and under the direction of faculty. Basic Qualifications MS degree or higher in Aerospace Engineering, Mechanical Engineering, or Civil Engineering with at least 8 years of relevant experience. Preferred Qualifications Experience in taking initiative and performing tasks with minimal guidance. Ability to interact with a group of individuals and set priorities for tasks to be performed. Ability to function in an engineering research laboratory environment. Background in some of the following is desirable: machining, electronics (hardware and software), optics (visible, infra-red, and X-rays), high-speed photography, instrumentation such as 3D printers, oscilloscopes, strain gages and load cells, and personal computers. Required Documents Resume Cover Letter

Company DescriptionJobs for Humanity is partnering with CEDARS-SINAI to build an inclusive and just employment ecosystem. Therefore, we prioritize individuals coming from the following communities: Refugee, Neurodivergent, Single Parent, Blind or Low Vision, Deaf or Hard of Hearing, Black, Hispanic, Asian, Military Veterans, the Elderly, the LGBTQ, and Justice Impacted individuals. This position is open to candidates who reside in and have the legal right to work in the country where the job is located. Company Name: CEDARS-SINAI Job Description Join us as we translate today's discoveries into tomorrow's medicine! The Postdoctoral Scientist in the Tatonetti Lab at Cedars-Sinai will create and lead research to improve drug safety by leveraging clinical and molecular data. In the Tatonetti Lab we use advanced data science methods, including artificial intelligence and machine learning, to investigate drug safety, drug-drug interactions, and cancer pharmacology. Using emerging resources, such as electronic health records (EHR) and genomics databases, we are working to advance the science of pharmacology with a focus on serving traditionally underrepresented populations. To learn more, visit TLab - Data-Driven Drug Safety (tatonettilab.org). Are you ready to be a part of breakthrough research? Working independently but in close cooperation and in consultation with the Dr. Tatonetti and other Research Scientists, the Postdoctoral Scientist will perform routine and complex laboratory procedures throughout training period. May develop, adapt, and implement new research techniques and protocols. Analyzes and interprets data. May assist in preparation of grant proposals. Participates in publications and presentations as author or co-author. Not responsible for generating grant funds. Primary Duties and Responsibilities: May assist in the preparation of grant proposals, but is not responsible for generating grant funds. May participate in publications and presentations as author or co-author. Designs and performs experiments. Will keep appropriate experimental records and documentation and analyze the results with the PI. Analyzes, interprets, summarizes, and compiles data. Operates and maintains equipment and instruments. May observe MD-patient or MD-human research subject interactions as it pertains directly to the research being performed. Education: Doctorate (MD, PhD, VMD, or DDS) in area directly related to field of research specialization. Experience and Skills: Acquires thorough technical and theoretical knowledge of research project and objectives during one to five (1-5) year post-doctoral appointment. Works independently on research projects designed by a mentor (typically the PI) within the area of specialization. Demonstrated aptitude to perform experimental protocols and procedures, including detailed data collection, and analysis, operation and maintenance of specialized equipment. Excellent written and oral communication skills are essential. Knowledge of safety standards. Working Title: Postdoctoral Scientist - Tatonetti Lab - Data-Driven Precision Pharmacology Department: Computational BioMedicine Business Entity: Cedars-Sinai Medical Center Job Category: Academic/Research Job Specialty: Postdoctoral Position Type: Full-time Shift Length: 8 hour shift Shift Type: Day Base Pay:$64,500.00 - $93,600.00

Perform behavioral, biochemical and electrophysical experiments on animals, analyze and report results. Required Qualifications 1. B.S. or higher degree in microbiology, biochemistry, molecular biology, cell biology or a related biological field; 2. Must have research laboratory experience (1-2 years minimum). 3. Must have experience in animal handling and observation.

Research Support Technician, Animal Breeding - (10032545) Description Join the forefront of groundbreaking research at City of Hope where we're changing lives and making a real difference in the fight against cancer, diabetes, and other life-threatening illnesses. Our dedicated and compassionate faculty and staff are driven by a common mission: Contribute to innovative approaches in predicting, preventing, and curing diseases, shaping the future of medicine through cutting-edge research. We're in search of a Research Support Technician - Animal Breeding to join our Animal Care Program team. The Research Support Technician is responsible for performing tasks and procedures associated with managing the production of research animal breeding colonies, including mating, weaning, animal identification, tissue biopsy, data collection, and communication with researchers using these services. As a successful candidate, you will:Monitor animal health and report any signs of illness or distress. Maintain clean cages, ensure food and water availability, and support overall animal well-being. Follow breeding plans, wean and separate litters, perform tissue biopsies, and animal identification. Accurately document breeding and husbandry activities; respond to researcher inquiries. Monitor and report environmental conditions and equipment issues in animal rooms. Clean and sanitize animal holding areas and support spaces regularly. Perform weekly animal census, reconcile discrepancies, and manage animal transfers. Assist with procedures including restraint, sample collection, and humane euthanasia. Qualifications Your qualifications should include High School or equivalent. No animal breeding experience required; 2 or more years of experience working in a laboratory animal care or veterinary technician position or related field. Required Certification/Licensure:AALAS ALAT certification (or obtained within 12 months of hire). City of Hope employees pay is based on the following criteria: work experience, qualifications, and work location. City of Hope is an equal opportunity employer. To learn more about our Comprehensive Benefits, please CLICK HERE. Primary Location: United States-California-DuarteJob: ResearchWork Force Type: OnsiteShift: DaysJob Posting: Oct 23, 2025Minimum Hourly Rate ($): 23. 339800Maximum Hourly Rate ($): 30. 394800

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