Microbiologist jobs in Manhattan Beach, CA - 541 jobs

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

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

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. Tuesday through Saturday, 9:00 AM to 5:30 PM

EASTVALE, California, United States of America At Solina, our community of close to 5,000 people share a passion for food and live our entrepreneurial culture. We design customised savoury solutions for our clients operating in the food industry, food service, butchery and nutrition markets. With sustainability at the heart of our business model, we aim to produce food that is good in every sense of the word: delicious, nourishing, affordable, sustainable and convenient. Solina is a fast-growing business, with around 50 production sites and R&D laboratories present in more than 19 countries mainly in Europe and North America. By constantly rethinking culinary solutions, we make food matter for people and the planet. If you're ready for a new adventure in a dynamic, expanding, passionate, international company, join us ! Solina USA, is a proud Solina Group company, specializing in the creation of customized seasonings and sauces. We take pride in our four strategically located production facilities across the United States which empower us to deliver high-quality, innovative flavor solutions efficiently to our customers. Our focus is on catering to Quick Service Restaurants, Fast casual, Casual dining, and food manufacturers, where our commitment lies in providing exceptional flavor solutions tailored to their unique needs. Solina USA has a proven national reputation of providing an exceptional customer experience by providing a high-quality product at a cost-competitive price point. We create dynamic relationships where our creativity can be visible through our customers culinary vision making "Food Matter." SUMMARY OF POSITION The Corporate Microbiologist is a key technical leader responsible for ensuring the microbiological safety, quality, and regulatory compliance of the company's portfolio of dressings, sauces, and spice blends. This role serves as the company's Process Authority for acidified foods, providing expert review, validation, and oversight of thermal and acidification processes in accordance with FDA requirements. In addition, the Corporate Microbiologist partners closely with R&D, Technical Services, Regulatory Affairs, Operations, and Quality teams to guide food safety decisions throughout the product lifecycle-from concept development to commercialization. The ideal candidate brings deep expertise in food microbiology, strong communication skills, and the ability to influence cross-functional teams. ESSENTIAL FUNCTIONS This document in no way states or implies that these are the only duties to be performed by the employee occupying the position. * Provide and apply technical knowledge (data, literature, etc.) and leadership to assure that the manufacturing processes and environments are microbiologically safe for the production of food products. * Evaluate and provide guidance on proper design of food processing equipment to world-class RTE standards. * Conduct and document data based risk assessments using technical, scientific, regulatory, and industry inputs. This include active review, interpretation, and communication of recommendations for food safety assessments or investigations. * Interpret sensitive food safety related technical information and provide objective science based recommendations. * Process Authority & Regulatory Compliance (Acidified Foods) o Serve as the company's designated Process Authority for acidified food products, ensuring compliance with appropriate FDA regulations. o Review, validate, and approve acidified product formulations, pH targets, critical factors, and thermal/hold processes. o Create, verify, and maintain process filings and scheduled processes for the FDA. o Conduct or oversee validation studies, challenge studies, and hazard assessments to support product safety. * Food Microbiology & Safety Expertise o Provide subject-matter expertise on microbiological hazards, shelf-life, and preservation strategies for new and existing products. o Support the design and interpretation of microbiological testing plans, challenge studies, and environmental monitoring programs. o Evaluate ingredient and process changes for microbiological impact and risk. o Develop and maintain internal microbiological specifications and guidelines. * Product Development Support o Partner with R&D and Technical Services during formulation and scale-up to ensure food safety is built into all product designs. o Review new product formulations, processing conditions, and packaging selections for microbiological viability and regulatory compliance. * Quality Systems & Continuous Improvement o Provide technical leadership for investigations of microbiological deviations, contamination events, and shelf-life failures. o Deliver internal training on microbiology, sanitation, process controls, and food safety topics to enhance organizational capability. * Communicate complex scientific concepts in a clear, actionable manner to both technical and non-technical stakeholders. * Maintain abreast of current and evolving food safety considerations and best practices. Remain current on evolving food safety considerations and best practices, including US regulatory requirements related to acidified foods, thermal processing, and low-acid canned foods, advising the organization on implications. REQUIRED SKILLS, EDUCATION, AND EXPERIENCE * PhD in Food Microbiology, Food Science, Microbiology, or related discipline (Master's with extensive industry experience may be considered). * Certified Process Authority preferred; willingness and ability to become certified if not already. * Minimum 5-8 years of experience in food manufacturing, food microbiology, process validation, or related roles. * Strong working knowledge of FDA regulations governing acidified foods (21 CFR 114), food safety plans, and microbiological risk management. * Demonstrated experience conducting validation studies, challenge studies, and shelf-life assessments. * Ability to translate microbiological concepts into practical manufacturing and product development recommendations. PREFERRED QUALIFICATIONS * Functional food safety expert in RTE manufacturing. In-depth knowledge of food safety, food microbiology, manufacturing processes, food regulations, sanitary design and quality management. * Experience in dressings, sauces, condiments, emulsions, marinades, RTU/RTS sauces, or dry spice blends. * Knowledge of thermal processing, pH control systems, and ingredient interactions affecting microbial stability. * Experience supporting FDA process filings and working directly with regulatory agencies. * Familiarity with environmental monitoring programs and pathogen control strategies. * Exceptional communication, documentation, and cross-functional collaboration skills. * Ability to work and interact effectively with all levels in the organization including Plant employees, Peers, and Senior Leaders * Ability to work in a multicultural environment with respect and sensitivity for diversity SUPERVISORY RESPONSIBILITY * None TRAVEL REQUIREMENTS 0-15% WORKING CONDITIONS Working conditions described here are representative of those experienced by an employee daily while performing this job's functions. * Typically sits for extended periods at a computer workstation. * Ability to work in lab, pilot plant, and plant environments when required. * May be required to work weekends to meet department and business demands. SPECIAL REQUIREMENTS Employment is contingent upon successfully passing an employee reference check, criminal background check, and drug screening. We are open to talents of all backgrounds. Our recruitment process is based on competences, and we openly welcome all candidates of all types according to our DEI Commitment

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.

* 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 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.

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.

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

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: **************

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!!!

Under supervision this position will work closely with Senior Researchers assisting in the design and implementation of research studies. Specific Responsibilities/Accountabilities * Handles administrative support duties for the grant (e.g., scheduling of internal meetings; staff meeting agenda preparation). * Supervises student workers on research tasks and supports the research of senior researchers. * Conducts basic data analysis with supervision from senior researchers. * With support from senior researchers, manage large volumes of quantitative data (including quality control), develops and maintains electronic codebooks of all databases. * Transcribe audio and video data to translate into quantitative metrics. * Assist seniors researchers with creating sophisticated PowerPoint presentations. * Synthesize literature and assist with development of instruments/measures. * Perform other duties as assigned or requested. Loyola Marymount University Expectations Exhibit behavior that supports the mission, vision, and values of the university. Communicate and employ interpersonal actions that model high standards of professional, responsible, accountable, and ethical conduct. Demonstrate a commitment to outstanding customer service. Requisite Qualifications * Typically a Bachelors Degree in Psychology, Sociology or Political Science or related field or equivalent experience. Incumbent will be expected to continue upgrading knowledge, skills, and abilities needed to keep abreast of methods used in the lab as well as regulation/policy changes. * Previous psychological or educational research work experience in an academic research setting. * Previous research experience and some experience with quantitative skills, including knowledge of statistics; * Strong organizational skills and a track record of working collaboratively with others in professional or extracurricular settings * Ability to be highly organized to facilitate record-keeping, data management, managing multiple responsibilities and collaboration with student research assistants. Demonstrated ability to work independently and collaboratively. * High intrinsic motivation and excellent self-management. Ability to take responsibility in meeting deadlines and making progress without direct supervision. * Exemplary communication skills (both written and oral). * Demonstrated computer competency and preferably knowledgeable of Word, PowerPoint, Excel, Qualtrics and SPSS. The above statements are intended to describe the general nature and level of work being performed. They are not intended to be construed as an exhaustive list of all responsibilities, duties and skills required of personnel so classified. Staff Regular Salary range $22.26 - $26.68 Salary commensurate with education and experience. Please note that this position may not be eligible for visa sponsorship now or in the future. Loyola Marymount University, a Carnegie classified R2 institution in the mainstream of American Catholic higher education, seeks outstanding applicants who value its mission and share its commitment to inclusive excellence, the education of the whole person, and the building of a just society. LMU is an equal opportunity employer committed to providing an environment free from discrimination and harassment as defined by federal, state and local law. We invite all persons in the full diversity of their being, life experience, and beliefs to apply. (Visit *********** for more information.)

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 Bachelor's degree 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

Seeking a part-time technician to aid in ecological research projects relating to plant competition, climate change, and microclimates. Hours are flexible. Specific duties: assist in the construction, set-up, and maintenance of the experiments, with responsibilities including building project infrastructure; collecting soil resource, plant trait, and plant diversity data; collecting and weighing seeds; digitizing and quality-checking data; and other related tasks as needed. All skills can be taught on the job. Required qualifications: Must have enthusiasm for learning new skills, be able to work well independently, be adaptable, reliable, detail-oriented, well-organized, and have good communication skills. Must be comfortable working in laboratories, workshops, and outdoors, including in adverse weather conditions typical of northern California. Must be comfortable lifting 25 pounds and occasionally engaging in strenuous physical activity in the field. Preferred qualifications: Experience with plant identification, especially in California serpentine grassland ecosystems Experience with data management, including maintaining a high-quality research notebook Experience with workshop and technical skills, including building simple structures out of wood, plastic, or other materials, or with soldering and cutting and stripping cables Knowledge of basic field first aid Degree or enrollment in courses in biology, environmental sciences, engineering, earth systems, or a related field To apply, please submit a resume or CV and a one-page cover letter. Questions can be directed to: Andrea Nebhut at ***************************. Applications are due 11/30/25.

Description Looking to join a passionate team dedicated to developing and manufacturing life-saving biopharmaceuticals? Avid Bioservices is a leading clinical and commercial biologics CDMO focused on creating innovative solutions to meet the needs of our clients and improve patient outcomes. Your Role: As a Sr. Microbiologist, Quality Control, you will lead the way in ensuring compliance with environmental regulations and Good Manufacturing Practices (GMP) by performing microbiological testing in a biopharmaceutical manufacturing organization. You will utilize state-of-the-art technology to monitor air, water, and surfaces for potential contaminants, inoculate microbial cultures for growth promotion testing, and perform bioburden testing. You will also review and trend data, generate charts, and maintain inventory of supplies. Your work will contribute to the production of life-saving biopharmaceuticals, making a positive impact on public health and the environment. Perform bioburden testing of water and in-process samples per USP, EP requirements, and gram staining of recovered microorganisms. Read EM plates and document results on relevant forms. Perform growth promotion testing. Perform Trending in LIMS (MODA or Labware). Maintain inventory of department supplies and place purchase orders. Inoculate microbial cultures for growth promotion testing. Prepare cultures to send out for identification when needed. Support investigations for EM out-of-limit results, including notification and re-testing of alert and action OOLs. Perform data review of environmental monitoring and assist in the preparation of environmental monitoring data trending reports. Monitor temperatures of Manufacturing and Microbiological QC refrigerators, freezers, cryo-freezers, and cold-room area. Other tasks as assigned. Minimum Qualifications: B.S. in Microbiology or related field with a minimum of 4-5 years of experience in a GMP facility working in a Microbiology lab; or master's degree in microbiology or related field with a minimum of 1-3 years of experience. Experience in performing the following tasks on a routine basis: Bioburden testing of water systems, raw materials, in-process materials/components, and finished product. Gram staining and experience with colony morphology. Aseptic microbiological techniques used in the microbiology lab to prevent contamination and cross-contamination. Trend Report and/or Protocol writing. Support Investigations to determine root cause and corrective action. Growth promotion testing. Knowledge of aseptic techniques and behavior. Must have knowledge of cGMP and should have necessary skills working in controlled environments. Experience with LIMS (preferable Labware and or MODA) Working knowledge of USP, EP, and Annex 1. Position Type/Expected Hours of Work: This role is a full-time position with a Sunday through Wednesday schedule, working 10 hours each day (4 days x 10 hours), with operating hours typically from 7:00am to 6:00pm. Compensation: We offer competitive compensation packages for this role, including a base salary, performance-based bonuses, and comprehensive benefits such as health, dental, and vision insurance, 401(k) matching, and paid time off. The compensation range for this role is $65,800 to $75,000 annually depending on experience and qualifications. Additionally, we offer opportunities for career growth and development as well as a supportive and inclusive work environment. Who you are: You have a "bring it on!" team player approach and an unshakable positive attitude, always ready to tackle anything that comes your way. Your written and verbal skills are out of this world, and you communicate with clarity and confidence. You have exceptional multitasking skills and an unparalleled attention to detail that ensure the smooth running of everything. You are a master at building relationships, capable of establishing connections with anyone, be it team members, clients, vendors, or suppliers. Physical Demands & Work Environment: In this dynamic role, expect a blend of regular activities like sitting, standing, and walking, with occasional physically engaging tasks such as lifting objects up to 25 pounds. The work environment might expose you to electrical shocks, toxic chemicals, vibrations, or loud noise levels occasionally. However, reasonable accommodations are available to enable individuals with different abilities to perform effectively, ensuring a supportive and adaptable work setting. Your visual acuity, including close, distance, and color vision, will be essential in navigating through the diverse day-to-day demands of this position.

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

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.