Microbiologist jobs in Santa Monica, CA - 267 jobs

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

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

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

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 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

- Prepare samples for analytical and microbiological testing of nutraceutical products, supplement ingredients, utilities, and environmental samples. - Perform Quality Control microbiological testing for food and nutraceutical manufactured products. - Conduct environmental monitoring of cleanrooms, including air, surface, and personnel monitoring. - Collect water samples per approved schedules and ensure timely testing and documentation. - Perform and review microbiological assays, including: o Gram stain o Sterility testing o Microbial identification o Growth promotion testing o Plate reading and interpretation - Perform and review visual inspection of finished products. - Perform microbiological utility testing, including water system monitoring. - Perform and oversee microbiological testing of probiotic raw materials and finished products, including: o Enumeration of probiotic strains o Strain verification o Stability and viability assessment - Enter data accurately into laboratory systems, trend microbiological data, and prepare reports and presentations for management review. - Assist with investigations related to out-of-specification (OOS) results and deviations associated with microbiological testing. - Perform routine maintenance and cleaning of laboratory equipment and laboratory spaces. - Review and approve final product microbiological test results to support product release. - Support audits and inspections (internal, customer, NSF, regulatory) as needed. - Perform other duties as assigned to support Quality and Manufacturing operations. Skills Environmental monitoring, gram staining, sterility testing, Microbiology, Aseptic technique, Quality control, Bioburden, Plating, Media, Sop, swabbing, strain verification, enumeration of probiotic strains, plate reading, probiotic raw materials, trending reports, deviation, out of spec, water testing, air monitoring, surface testing, NSF, GMP, microbiological testing Top Skills Details Environmental monitoring,gram staining,sterility testing,Microbiology Additional Skills & Qualifications - Bachelor's degree in microbiology, Biology, or a related scientific discipline. - Hands-on experience with microbiological techniques, including: o Environmental air monitoring o Water testing o Surface monitoring - Experience with aseptic techniques and cleanroom operations. - Ability to grow and work within aseptic core and support cleanroom areas. - Knowledge of GMP regulations, SOPs, and Quality Control processes in a commercial manufacturing environment. - Ability to lift- up to approximately 25 lbs. - Ability to pass a vision exam for visual inspection activities. - Proficiency in Microsoft Word, Excel, PowerPoint, and related applications. - Strong interpersonal, verbal, and written communication skills. - Ability to work effectively in a fast-paced, small company environment with minimal supervision. - Flexibility to adjust workload based on changing priorities and to work overtime as needed. Preferred Qualifications - Experience with probiotic microbiological testing, including enumeration, identification, and stability studies of probiotic strains (strongly preferred). - Experience in dietary supplement, nutraceutical, food, or pharmaceutical manufacturing environments. - Familiarity with NSF certification requirements and regulatory expectations for Experience Level Intermediate Level Job Type & Location This is a Contract to Hire position based out of Chatsworth, CA. Pay and Benefits The pay range for this position is $20.00 - $40.00/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: - Medical, dental & vision - Critical Illness, Accident, and Hospital - 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available - Life Insurance (Voluntary Life & AD&D for the employee and dependents) - Short and long-term disability - Health Spending Account (HSA) - Transportation benefits - Employee Assistance Program - Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in Chatsworth,CA. Application Deadline This position is anticipated to close on Jan 23, 2026. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com (%20actalentaccommodation@actalentservices.com) for other accommodation options.

Job Description Clinical Laboratory Scientist (CLS) / Core Laboratory 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) 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 high-complexity testing in Chemistry, Hematology, Coagulation, Urinalysis, and related Core Lab sections. Analyze and verify patient results in accordance with laboratory procedures and regulatory requirements (CLIA, CAP, and state guidelines). Operate, calibrate, and maintain laboratory analyzers and instrumentation, troubleshooting issues as needed Review, interpret, and release laboratory test results in the Laboratory Information System (LIS) with accuracy and timeliness. . Perform and document quality control, proficiency testing, and participate in quality improvement initiatives. Adhere to all biosafety, infection control, and PPE requirements to maintain a safe laboratory environment. Collaborate with pathologists, physicians, and other laboratory staff to support accurate clinical decision-making. Remain current with Core Lab best practices, instrumentation updates, and changes in testing methodologies. 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. Experience with Molecular. Additional Requirements This position is an on-site at Primex Clinical Laboratories, Inc. 16742 Stagg St. #120 Van Nuys, CA 91406. Compliance with PPE and safety protocols required. Ability to stand, walk, bend, and lift as needed for laboratory operations. Must demonstrate a cooperative, team-oriented approach to working with colleagues. 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.

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).

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!!!

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 Are you ready to be a part of breakthrough research? Principal Investigator, Joshua Sasine, MD, PhD is looking for a Postdoctoral Scientist to join the team! The Sasine Laboratory focuses on three areas: • The communication between the bone marrow microenvironment and multiple myeloma, a cancer of antibody-secreting plasma cells. • Macromolecule delivery via extracellular vesicles. • Chimeric antigen receptor (CAR) T cell therapy interactions with normal myeloid cells. The Sasine lab has characterized paracrine factors that govern the biology of hematopoietic stem cells and hematopoietic cancers. Now, we are leveraging our expertise in this area to create biotechnology to intervene on these processes. To learn more about this important work, please visit the Sasine Laboratory website. We are actively seeking a Postdoctoral Scientist who will work independently but in close cooperation and in consultation with the Principal Investigator and Research Associates. In this role, the candidate will perform routine and complex laboratory procedures throughout the training period as they develop, adapt, and implement new research techniques and protocols. The candidate will analyze and interpret data and may assist in preparation of grant proposals. The candidate will participate in publications and presentations as the first author or co-author. The individual in this position will not be responsible for generating grant funds. Primary Job Duties and Responsibilities: May assist in 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 P.I. Analyzes, interprets, summarizes and compiles data. Operates and maintains equipment and instruments Education: Doctorate (MD, PhD, VMD, or DDS) in area directly related to field of research specialization. Experience and Skills: Highly motivated and works independently on research projects designed by a mentor (typically the PI) within area of specialization. Acquires thorough technical and theoretical knowledge of research project and objectives during one to five (1-5) year post-doctoral appointment. Demonstrated aptitude to perform experimental protocols and procedures, including detailed data collection, and analysis, and operation and maintenance of specialized equipment. Knowledge of safety standards and maintenance of specialized equipment. Education: Doctorate (MD, PhD, VMD, or DDS) in area directly related to field of research specialization. Experience: Highly motivated and works independently on research projects designed by a mentor (typically the PI) within area of specialization. Acquires thorough technical and theoretical knowledge of research project and objectives during one to five (1-5) year post-doctoral appointment. Demonstrated aptitude to perform experimental protocols and procedures, including detailed data collection, and analysis, and operation and maintenance of specialized equipment. Knowledge of safety standards and maintenance of specialized equipment. Physical Demands: Able to perform moderate lifting. Able to sit, stand and walk for prolonged periods of time. Able to read papers and online documents. Able to operate standard office equipment. Able to exercise physical ability and perspective acuity to satisfactorily perform essential job functions. Working Title: Postdoctoral Scientist - Sasine Lab - Hematology & Cellular Therapy Department: Home Dept - Medicine Research 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

This position serves as support for the Associate Dean for Enrollment Management, the Supervisor for Personnel and Curriculum and the Student Success Support Analyst. Incumbents learn to assist in gathering resource data in areas of scheduling, enrollment, curriculum, personnel, and hiring. Will learn to compile and analyze data for historical trend tracking, and crafts reports and presentations. Will learn to update and maintain College data tracking spreadsheets and file records. Provides continuity in policy and procedures, processes all assignments, meets all deadlines, and completes all paperwork required. Communicates and disseminates information to various units in the University. Key Responsibilities * Provides College research support by gathering data, conducing analyses, and preparing reports. * Assists with personnel, curriculum and scheduling processes with a focus on the data analytic aspects of these processes. * Assists with the development of procedures, policies and practices and then communicates these to college and university units. * Assists assembling surveys on-line processes for Assigned Time, Travel Awards, Equipment and Materials calls, voting, surveys for evaluations and new surveys needed for personnel and fiscal assignments. Department CLA Administration Time Base 1.0 time-base, 40 hours per week. Duration of Appointment This is a temporary position for 1 year with no permanent status granted. Temporary assignments may expire prior to the ending date. Classification Research Technician I Compensation Salary placement is determined by the education, experience, and qualifications the candidate brings to the position, internal equity, and the hiring department's fiscal resources. * Hiring Range: The hiring range for this position is $4,595 (Step 1) - $4,974 (Step 5) per month commensurate with candidate's education, experience, skills, and training. * CSU Classification Salary Range: The CSU Classification Salary Range for this position is $4,595 (Step 1) - $6,694 (Step 20) per month. Benefits At California State University (CSU), we prioritize the health, growth, and success of our employees. Our benefits program is just one way the CSU demonstrates its dedication to your success and well-being. Employees with a .50 FTE appointment exceeding six months and one day are eligible for full benefits. Eligible employees have access to this comprehensive benefits package, which includes: * Generous Paid Time Off: Up to 24 vacation days per year (based on employee group and/or service), 14 paid holidays, and 12 sick days annually with unlimited accrual. * Comprehensive Health Coverage: A variety of medical, dental, and vision plans to suit your needs. * Retirement Plans: Participation in CalPERS defined benefit plan and access to voluntary savings plans like 403(b), 401(k), and 457. * Educational Benefits: Tuition fee waivers for employees and eligible dependents. * Employee Assistance Program (EAP): Confidential counseling and support services for employees and their families. * Additional Perks: Access to wellness programs, professional development opportunities, and various insurance options including life, disability, and pet insurance. The CSU offers comprehensive benefit packages tailored to individual bargaining units. Candidates are encouraged to review the applicable CSU Employee Benefits Summary for details on the benefits available. Additionally, the CSU Total Compensation Calculator is available to help prospective employees understand the full value of the CSU benefits package and how it complements your base salary. Knowledge, Skills, and Abilities The ideal candidate is capable of carrying out professionally complex assignments while independently planning and developing sound approaches and solutions that meet departmental program, faculty, and student needs. They possess strong knowledge of budget management, fiscal resource allocation, and accountability practices. This individual effectively represents the department to all constituencies, delivering essential information through clear written and oral communication. They excel at building and maintaining collaborative working relationships with program faculty, academic departments, the dean's office, and various campus and community partners. The ideal candidate also demonstrates solid working knowledge of Windows, Word, email, spreadsheets, databases, webpages, and CMS platforms, and is adept at creating and implementing programs and events that strengthen engagement among students, faculty, the campus community, and local partners. Ability to communicate with an ethnically and culturally diverse campus community. Ability to follow all university policies, procedures, and guidelines including but not limited to safety, civility, information security, and non-discrimination policies and procedures. Ability to contribute to a positive university experience for each and every student and assist in achieving the university's commitment to a "vision of excellence." Education and Experience * Equivalent to a bachelor's degree in a related field and one year of experience in technical research or statistical work required. * Academic department or program experience preferred. Application Procedures Click "Apply Now" to complete the CSULB Online Employment Application. Please fill out the application completely. It is important that all sections of the online application are completed fully and accurately. Be sure to include all relevant education and experience. Your application will be used to determine whether you meet the minimum qualifications for this position. Physical Summary Sedentary work - Involves mainly sitting. Walking and standing are minimal. Lifting is limited to lightweight objects. (10 pounds or less). Additional Information CSULB is not a sponsoring agency for staff and management positions (i.e. H-1B Visas). A background check (including a criminal records check) must be completed satisfactorily and is required for employment. CSULB will make a conditional offer of employment, which may be rescinded if the background check reveals disqualifying information, and/or it is discovered that the candidate knowingly withheld or falsified information. Failure to satisfactorily complete the background check may affect the continued employment of a current CSU employee who was conditionally offered the position. Due to the nature of this position, current CSULB employees are subject to a criminal record check unless they have successfully completed a criminal background check through CSULB within the past 12 months. Equal Employment Statement Consistent with California law and federal civil rights laws, CSULB provides equal opportunity in employment without unlawful discrimination or preferential treatment based on race, sex, color, ethnicity, national origin, or other protected status. CSULB complies with Title VI of the Civil Rights Act of 1964, Title IX of the Education Amendments of 1972, the Americans with Disabilities Act (ADA), Section 504 of the Rehabilitation Act, the California Equity in Higher Education Act, California's Proposition 209 (Art. I, Section 31 of the California Constitution), other applicable state and federal anti-discrimination laws, and CSU's Nondiscrimination Policy. We prohibit discriminatory preferential treatment, segregation based on race or any other protected status, and all forms of discrimination, harassment, and retaliation in all university programs, policies, and practices. California State University Long Beach expects respectful, professional behavior from its employees in all situations. Acts of harassment or abusive conduct are prohibited. Demonstrated appropriate professional behavior, treating others with civility and respect, and refusing to tolerate abusive conduct is expected of all employees. Accommodations We provide reasonable accommodations to applicants and employees with disabilities. Applicants with questions about access or requiring a reasonable accommodation for any part of the application or hiring process should contact StaffHR-Accommodations@csulb.edu. Out of State Employment Policy California State University, Long Beach, as part of the CSU system, is a State of California Employer. As such, the University requires all employees upon date of hire to reside in the State of California. As of January 1, 2022 the CSU Out-of-State Employment Policy prohibits the hiring of employees to perform CSU-related work outside the state of California. Advertised: Jan 16 2026 Pacific Standard Time Applications close: Jan 30 2026 Pacific Standard Time

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

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 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 Microbiology Technician to join our growing team! JOB SUMMARY Prepare samples for analytical and microbiological testing of nutraceutical products and supplements ingredients, and environmentals. The role is responsible for the application of approved microbiological techniques and methodologies used in analytical testing. ESSENTIAL RESPONSIBILITIES * Assist in microbial challenge testing of new products to determine adequacy of preservation. * Bioburden panel testing, water testing, environmental testing (ie air plates, swabs, conductivity) * Apply aseptic techniques in daily workload. * Inventory and report expendable supplies/materials needed for testing requirements * Provide routine preventive maintenance by daily cleaning, sanitizing, and trash disposal * Perform quality control monitoring by taking incubator temperatures, inoculating control organisms, running media controls, etc. * Maintain laboratory condition, to include equipment, supplies * Perform all activities in a neat, safe, hygienic, and efficient manner * Prepare media for microbial quality and preservative adequacy testing. * Document media preparation and media control information in appropriate logbooks. * Maintain appropriate notebooks and computer logs required for the department. * Organize the destruction of product discards and assist with special projects. * Share information in an open, and timely manner with Supervisor * Perform other duties as assigned. MINIMUM QUALIFICATIONS: * BS degree in microbiology or related field with 1-2 years of lab experience. * At minimum, 1 or more years of Quality Assurance or Microbiological testing experience in the cosmetic, nutritional, or pharmaceutical industries * Able to handle multiple tasks and work in a fast-paced environment. * Able to adapt to changes to improve company processes. * Able to carry up to 50 pounds. * Able to stand and sit for long periods of time. * Must be able to rotate one weekend day. PHYSICAL DEMANDS * Dexterity of hands and fingers to operate a computer keyboard, mouse and to handle other communications/computer components * Potential exposure to odors, fumes, airborne particles, hazardous chemicals, and microbiological pathogens * Noise level varies from quiet to loud * Temperature varies from hot to cold * Interactive and fast-paced team oriented tasks * Occasionally lift and/or move up to 25 pounds. * Color vision and depth perception Benefits: * Progressive 401k Retirement Savings Plan * Employer Paid Short- Term and Long-Term Disability, and Life Insurance * Group Medical * Tuition Reimbursement * Flexible Spending Accounts * Dental * Paid Holidays and Time Off * 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.

The Microbiology & Sterilization Specialist will be instrumental in supporting integration, remediation, and sustainment activities related to sterilization, microbiology, and environmental control processes. This role involves assessing current practices, updating procedures, and ensuring compliance with applicable standards and regulatory requirements. The specialist will work closely with cross-functional teams to maintain robust sterilization and microbiological control programs that ensure product quality and patient safety. Responsibilities * Conduct updated gap assessments of existing microbiology and sterilization processes, procedures, and controls. * Identify deficiencies and develop remediation plans to align with regulatory expectations and industry standards. * Update, revise, and improve procedures related to sterilization, microbiological testing, and environmental monitoring. * Serve as a steward for the enforcement and implementation of relevant standards and regulations within the Quality and Sterilization domains. * Ensure alignment with ISO (EO sterilization), FDA regulations, GMP requirements, and internal quality system procedures. * Support routine GQO activities related to sterilization oversight and environmental control programs. * Provide technical guidance on bioburden, endotoxin testing, and environmental monitoring practices. * Support cleanroom operations, sterilization validation activities (IQ/OQ/PQ), and ongoing compliance initiatives. * Collaborate with cross-functional partners to ensure consistent application of microbiological and sterilization best practices. Essential Skills * Minimum 3 years of experience in EO sterilization or microbiology within the medical device or pharmaceutical industry. * Hands-on experience with sterilization validation (IQ/OQ/PQ), cleanroom operations, and regulatory compliance. * Demonstrated ability to assess and remediate sterilization or microbiological processes. Job Type & Location This is a Contract position based out of Irvine, CA. Pay and Benefits The pay range for this position is $35.00 - $42.00/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life & AD&D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in Irvine,CA. Application Deadline This position is anticipated to close on Jan 23, 2026. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Research Technician will be responsible for carrying out administrative research tasks, including scheduling, managing receipts and preparing expense reports in Concur. Responsibilities Track and manage lab expenses, including receipt documentation and financial reporting. Perform administrative duties, including Concur expense report management and scheduling. Support general lab operations and perform other duties as assigned. Required Qualifications Experience with Concur for expense tracking and report management. Proficiency in Microsoft Office Suite (Excel, Word, PowerPoint, Outlook). Data entry and management skills using Excel or other software. Strong organizational and problem-solving skills. Ability to work both independently and collaboratively in a research environment.

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

Job DescriptionBioPhase Solutions specializes in recruiting top talented professionals for Southern California's Scientific community. We are currently looking for a QC Microbiologist to work for a Greater Los Angeles area cosmetics contract manufacturing company. Pay Rate: $20-24/hour depending on experience. 2nd shift: 1:00pm - 9:30pm plus OT and weekends as needed Summary:Responsible for all aspects of microbiological issues, including but not limited to the following: writing and validating microbiological procedures, testing samples and interpretation of results. Responsible for obtaining samples and coordination the timing and testing of each sample as described in the SOP. Responsibilities: Perform microbiological testing of bulk samples, finished goods, raw materials and other samples as outlined in SOP's. Perform preservative efficiency/challenge testing. Review, interpret and perform test protocols as directed. Develop and coordinate document control related to microbiological testing. Maintains and coordinates equipment calibration to support QC compliance in key aspects. Maintain various logbooks with departmental data. Support the department by typing memos, reports and spreadsheets with distribution and filing as required. Email, fax or make telephone calls as needed. Understand, exercise, and monitor all GMP and safety requirements and procedures in the work environment. Support other areas of QC with clerical support as needed. Will require use of gloves, safety glasses Performs other duties as assigned. Experience: Bachelor's Degree in Microbiology or related field. At a minimum, completed two years of course work and laboratory experience in Microbiology. Knowledge of microbiological methodologies and practices. Excellent English written and verbal communication skills. Advanced statistical and mathematical skills. Please send resumes to *********************** and visit our website at ******************* for additional job opportunities!!!

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