public health microbiologist

Hoag Health System

<div>Primary Duties and Responsibilities
The Clinical Lab Scientist II (CLS II) performs a range of standard and technically demanding procedures and analysis on patient specimens in one or more clinical laboratory disciplines. This role recognizes critical and significant findings, reports test results, and maintains records of patient tests. Also, recognizes technical, instrumental, or physiological problems that could adversely affect tests or results, resolves, and documents. Performs calibration and maintenance of laboratory instruments. Adheres to quality control protocols to ensure accuracy of results. Monitors the accuracy and precision of all laboratory tests personally performed. Actively participates in continuing education programs. Communicates technical and general information to manager and medical staff.
In addition to the above, the CLSII analyzes data for trends, ensures, departmental standard operating procedures and competency documents reflecting current practice, and documents nonconforming events. May act as lead on weekends or other periods of reduced staffing.
Projects an image of professionalism in communication, appearance and conduct. Supports the laboratory mission. Participates in the continuous quality improvement process. Maintains a working knowledge of departmental standard operating procedures. This knowledge may include the use of specialized instrumentation, quality control requirements, and preventative maintenance. Performs other duties as assigned.</div>
 <div></div>
 <div>Education and Experience
<ul><li>Baccalaureate Degree in medical technology or related science required.
</li><li>Two to three years relevant clinical laboratory experience as an CLS required.
</li></ul>License Required
Must meet and maintain current State of California licensure requirements for one of the following.
<ul><li>Clinical Laboratory Scientist
</li><li>One of the following Limited Clinical Laboratory Scientist:
<ul><li>CHEMISTRY - Clinical Chemist Scientist
</li><li>HEMATOLOGY/URINALYSIS - Hematologist Scientist
</li><li>TRANSFUSION SERVICE - Clinical Immunohematologist Scientist
</li><li>MICROBIOLOGY - Clinical Microbiologist Scientist / Public Health Microbiologist</li></ul></li></ul></div>

Clinical Lab Scientist II : Orange Coast Women's

Colgate-Palmolive

<div>No Relocation Assistance Offered 
Job Number #169860 - Hodges, South Carolina, United States 
 
Who We Are 
 
Colgate-Palmolive Company is a global consumer products company operating in over 200 countries specializing in Oral Care, Personal Care, Home Care, Skin Care, and Pet Nutrition. Our products are trusted in more households than any other brand in the world, making us a household name! 
 
Join Colgate-Palmolive, a caring, innovative growth company reimagining a healthier future for people, their pets, and our planet. Guided by our core values&mdash;Caring, Inclusive, and Courageous&mdash;we foster a culture that inspires our people to achieve common goals. Together, let's build a brighter, healthier future for all. 
Microbiologist
Join our Quality team in Greenwood, SC, and play a critical role in ensuring product safety and excellence! As the Microbiologist, you will be responsible for product and raw materials testing, troubleshooting, and the full implementation of the facility's Micro Control Plan. You'll drive continuous improvement initiatives and leverage your expertise to maintain our high quality and compliance standards in a 24/7 manufacturing environment. This is your opportunity to own laboratory quality control systems and influence key operational decisions.
Key Responsibilities:<ul><li>
Perform comprehensive microbiological testing of raw materials, water, work-in-process, and finished product for approval and release.</li><li>
Own the maintenance of the Laboratory Quality Control Systems and ensure cGMP compliance, including performing failure investigations and properly documenting Out of Specification (OOS) results.</li><li>
Lead the development and implementation of the plant-wide Microbiological Control Program.</li><li>
Support nonconformance resolution, identify corrective and preventative actions (CAPA), and provide related Microbiology</li><li>
Cleaning &amp; Sanitization training to plant employees and assist with product, equipment, and C&amp;S validations.</li><li>
Maintain and utilize Key Performance Indicators (KPIs) to drive continuous improvement, identify trends, and draw conclusions.</li></ul>
Required Qualifications:<ul><li>
B.S. in Microbiology or a related Science.</li><li>
Minimum 2-3 years of experience as a Microbiologist in a manufacturing laboratory work environment.</li><li>
Experience with basic lab equipment (e.g., pH meters, balances, Celsis Luminometer) and common microbiology lab instrumentation (e.g., autoclaves, biohazard cabinets).</li><li>
Demonstrated experience with general documentation practices and cGMP compliance, including notebooks and data entry forms with specific attention to detail.</li><li>
Familiarity with quality systems such as failure investigations, Corrective and Preventive Actions (CAPA), calibration, and change control.</li><li>
Ability and flexibility to work a rotating schedule to support a 24/7 plant facility operation.</li></ul>
Preferred Qualifications:<ul><li>
Working knowledge and practical experience with Good Laboratory Practices (GLP) and techniques such as Gram staining, microscopy, isolation plating, media preparation, and microorganism identification methods.</li><li>
Experience in an FDA-regulated environment or an industrial environment implementing cGMPs.</li><li>
Demonstrate Results Orientation and the ability to prioritize duties to get effective results.</li><li>
Experience with SAP &amp; LIMS</li></ul> 
Compensation and Benefits 
Salary Range $62,000.00 - $93,000.00 USD 
 
Pay is determined based on experience, qualifications, and location. Salaried employees may also be eligible for discretionary bonuses, profit-sharing, and long-term incentives for Executive-level roles. 
 
Benefits: Salaried employees enjoy a comprehensive benefits package, including medical, dental, vision, basic life insurance, paid parental leave, disability coverage, and participation in the 401(k) retirement plan with company matching contributions subject to eligibility requirements. Additional benefits include a minimum of 15 vacation/PTO days (hourly employees receive a minimum of 120 hours) and 13 paid holidays (vacation days are prorated based on the employee's hire date within the calendar year). Paid sick leave is adjusted based on role and location in accordance with local laws. Detailed information regarding paid sick leave entitlements will be provided to employees upon hiring and may be subject to adjustments based on changes in legislation or company policies. 
 
Our Commitment to Inclusion 
Our journey begins with our people&mdash;developing strong talent with diverse backgrounds and perspectives to best serve our consumers around the world and fostering an inclusive environment where everyone feels a true sense of belonging. We are dedicated to ensuring that each individual can be their authentic self, is treated with respect, and is empowered by leadership to contribute meaningfully to our business. 
 
Equal Opportunity Employer 
Colgate is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity, sexual orientation, national origin, ethnicity, age, disability, marital status, veteran status (United States positions), or any other characteristic protected by law. 
 
Reasonable accommodation during the application process is available for persons with disabilities. Please complete this request form should you require accommodation. 
 
For additional Colgate terms and conditions, please click here. 
 
#LI-On-site</div>

Microbiologist

Refined Reports Data

Key Responsibilities:<ul><li>Research and Analysis:</li><li>Conduct experiments to study microorganisms (bacteria, viruses, fungi, etc.) in controlled laboratory settings.</li><li>Investigate the interactions between microorganisms and human/animal/plant systems.</li><li>Perform genetic, biochemical, and microbiological analyses of samples.</li><li>Develop methods for isolating, identifying, and cultivating microorganisms.</li><li>Data Collection and Interpretation:</li><li>Analyze results from microbiological tests and research to identify patterns and implications.</li><li>Maintain accurate records of research findings, including laboratory notes, test results, and statistical data.</li><li>Utilize advanced software and technologies for data analysis and interpretation.</li><li>Microbial Culture and Identification:</li><li>Grow and maintain microbial cultures under various conditions (e.g., temperature, pH, salinity) to identify new strains or pathogens.</li><li>Prepare culture media and reagents for microbiological experiments.</li><li>Use microscopes, petri dishes, and other lab equipment to study microorganisms.</li><li>Quality Control and Safety Compliance:</li><li>Ensure compliance with safety standards and laboratory protocols, particularly in handling pathogenic microorganisms.</li><li>Develop and implement quality control measures to ensure the accuracy and reliability of test results.</li><li>Supervise laboratory technicians and assistants.</li><li>Reporting and Documentation:</li><li>Prepare detailed reports and research papers for publication in scientific journals or internal use.</li><li>Communicate findings to colleagues, clients, or stakeholders through presentations and meetings.</li><li>Assist in the preparation of grants and funding proposals for future research projects.</li><li>Collaboration:</li><li>Work with other scientists, clinicians, or regulatory bodies to contribute to broader scientific initiatives or public health goals.</li><li>Provide technical advice on microbiological issues to other departments, organizations, or public health agencies.</li><li>Skills and Qualifications:</li><li>Education:</li><li>Bachelor's degree in Microbiology, Biology, or a related field (entry-level).</li><li>Master's or Ph.D. in Microbiology or a specialized field may be required for advanced positions.</li><li>Technical Skills:</li><li>Strong understanding of microbiological laboratory techniques, including culturing, staining, and microscopy.</li><li>Proficiency in using laboratory equipment (e.g., autoclaves, PCR machines, spectrophotometers).</li><li>Familiarity with data analysis software (e.g., SPSS, R, Microsoft Excel).</li></ul>Job Types: Full-time, Permanent, FresherPay: &#8377;25,465.78 - &#8377;40,040.66 per monthBenefits:<ul><li>Health insurance</li><li>Paid sick time</li><li>Provident Fund</li></ul>Work Location: In person

Curium Pharmaceuticals

<div>About Curium
Curium is the world&rsquo;s largest nuclear medicine company with more than a century of industry experience. We develop, manufacture and distribute world-class radiopharmaceutical products to help patients around the globe. Our proven heritage combined with a pioneering approach are the hallmarks to deliver innovation, excellence and unparalleled service. 

With manufacturing facilities across Europe and the United States, Curium delivers SPECT, PET and therapeutic radiopharmaceutical solutions for life-threatening diseases to over 14 million patients annually. The name &lsquo;Curium&rsquo; honors the legacy of pioneering radioactive researchers Marie and Pierre Curie, after whom the radioactive element curium was named and emphasizes our focus on nuclear medicine. The tagline &lsquo;Life Forward&rsquo; represents our commitment to securing a brighter future for all those we serve: An enhanced quality of care for our patients. A trusted partner to our customers. A supportive employer to our valued team. 

<div><div><div><h2 class="jobSectionHeader">
Summary of Position</h2>
</div><div>
Perform assigned quality control activities within the Microbiology Department in order to comply with applicable SOP's and cGMPs. Work under limited supervision with considerable latitude for the use of initiative and independent judgment. Provide timely testing and notification of any aberrant occurrence to Management / Supervision that presents potential negative impact to manufactured or marketed product. Must have the ability to work collaboratively, multitask, and adapt to changing priorities and schedules. 


Work schedule: Monday - Friday 8am - 5pm</div></div><div><div><h2 class="jobSectionHeader"> 
Essential Functions</h2>
</div><div><ul><li>Author, revise, review and approve site procedures and policies related to Environmental Monitoring and Sterility as applicable.</li>
<li>Serve as lead investigator for Environmental Non-Conformance and OOS investigations, including root cause analysis, and implementation of corrective and preventative actions.</li>
<li>Employ aseptic techniques in the performance of testing per USP and Curium Standard Operating Procedures (SOP) and Standard Test Methods (STM) for Sterility, Endotoxin, Bioburden on drug products, intermediates and raw materials.</li>
<li>Train new employees in aseptic techniques.</li>
<li>Perform Growth Promotion testing per USP Method on various microbiological media.</li>
<li>Prepare and analyze Biological Indicators in support of various Validation and Qualification activities.</li>
<li>Read plates to quantify microbial growth and subculture pure isolates as required.</li>
<li>General laboratory housekeeping duties.</li>
<li>Collaborate with other team members to ensure the consistent and timely completion of all testing and other tasks in support of business needs.</li>
<li>Assist with laboratory investigations including OOS, root cause analysis, and implementation of corrective and preventative actions.</li>
<li>Ensure a safe and quality-minded working environment through conformance with training, general awareness, and compliance to safety/Quality guidelines and SOPs.</li>
<li>Ensure the maintenance of their department, premises, and equipment.</li>
<li>Perform all work in compliance with site safety and radiation protection guidelines.</li>
<li>Attend mandatory trainings as required by site regulatory requirements and management.</li>
<li>Perform other general duties associated with the position as required by supervision.</li>
<li>Must maintain operational compliance with US and international regulatory agencies and guidelines (i.e. FDA, EU, HC, TGA, PIC/S, ISO, USP, NRC, cGMP, etc.).</li>
</ul></div></div><div><div><h2 class="jobSectionHeader">Requirements</h2>
</div><div><ul><li>Bachelor Degree preferred, Associate Degree or completion of 4 college-level life science courses required.</li>
<li>Three or more years of relevant experience required.</li>
<li>Previous experience with aseptic process simulations preferred.</li>
<li>Quality and production experience in a cGMP / FDA regulated facility is required.</li>
<li>Good interpersonal skills, good hands on, analytical, problem solving and decision-making skills.</li>
<li>Excellent written and verbal communications skills.</li>
<li>Good computer skills, including utilizing personal computers and data entry programs.</li>
<li>Ability to work independently and with others to accomplish goals and priorities.</li>
<li>Flexibility and teamwork skills.</li>
<li>High level of energy and regular, consistent attendance.</li></ul> 

Working Conditions:
<ul><li>Willingness to work in plant producing radioactive materials and requiring all employees to participate in safety programs designed to minimize potential and/or actual exposure levels.</li>
<li>Responsibilities include the ability to lift up to 70 pounds, kneeling, crouching, twisting the upper body, walking, bending, stooping, pushing, pulling, reaching, must be able to physically negotiate stairs and evacuation ladders with or without accommodation, wear and operate safety equipment, enter vessels, and inspect equipment.</li>
<li>Material handling devices (e.g., hand truck, fork truck, and conveyors) are used when possible, however, use of proper lifting and movement techniques is necessary to prevent injury.</li>
<li>Must be willing to wear a variety of Personal Protective Equipment (PPE) and hearing protection as needed.</li>
<li>May be required to sit or stand for long periods of 8+ hours a day while performing duties.</li>
<li>Must possess good hand-eye coordination; close attention to detail is required.</li>
<li>Must be able to work indoors and outdoors with exposure to mechanical/moving parts, hazards including corrosive, flammable and toxic material, dust, dirt, odors, and irritants.</li>
<li>Willingness to complete safety training within allotted timeframes, and work in a team-based environment.</li>
<li>Must be able to work outside of regular work hours, including off shift, weekend, and holiday work as business needs require.</li>
</ul>
</div></div></div>Disclaimer
The above statements are intended to describe the general nature and level of work being performed by employees assigned to this classification. They are not intended to be construed as an exhaustive list of all responsibilities, duties and skills required of employees assigned to this position. 

Equal Opportunity Employer
Curium is an equal opportunity employer and believes everyone deserves respect, dignity and equality. All applicants will be considered for employment without attention to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran or disability status.</div>

Amros Pharmaceuticals

We're looking for a highly skilled Senior Microbiologist to join our pharmaceutical team.Requirements:Minimum of 2 years of hands-on experience as a Microbiologist within a regulated pharmaceutical company setting.Proven expertise in environmental monitoring, sterility testing, water testing, and microbial limit tests.Strong knowledge of GMP/GLP regulations.If you're ready to take the next step in your career and contribute to critical quality control operations, we want to hear from you!Job Type: Full-timeExperience:<ul><li>Pharmaceutical: 2 years (Preferred)</li></ul>Work Location: In person

Senior Microbiologist

Getz Pharma

<div>
 
 
 Job Summary :
 
 
 
 The incumbent must be able to support in microbiological testing and documentation. In addition, the candidate must be able to perform environmental monitoring in sterile and non-sterile production areas, and also perform microbiological tests.
 
 
 
 
 
 
 Job Responsibilities:
 
 
 <ul>
 <li>
 Implementation of cGMP and other regulatory standards to maintain and sustain performance of the Lab.
 </li>
 <li>
 Provide support in documentation during qualification and validation studies, during Audits, and area qualification
 </li>
 <li>
 Involvement and support during equipment qualifications, hold time studies and cleaning validation.
 </li>
 <li>
 Environmental monitoring of Microbiology and sterile production, and trend charting of Environmental monitoring results.
 </li>
 <li>
 Testing of stability products,
 </li>
 <li>
 Media preparation and GPT
 </li>
 <li>
 Identification of Environmental and water Isolates
 </li>
 <li>
 Sampling testing and Reporting of new PW plant.
 </li>
 <li>
 Maintenance of microbial cultures.
 </li>
 </ul>
 
 
 
 
 
 Key Requirements:
 
 
 <ul>
 <li>
 A minimum qualification of BS Microbiology/Biotechnology/Biosciences
 </li>
 <li>
 A minimum of 1-4 years of relevant work experience
 </li>
 <li>
 Understanding of Good Microbiological lab practices and 5s, and of Environmental monitoring of clean rooms and basic understanding of gowning procedures.
 </li>
 <li>
 Basic understanding of Media preparation, GPT test, lab equipment and process flow.
 </li>
 <li>
 Understanding of identification steps, microbial limit test,bioburden, and culture preservation
 </li>
 </ul>
 
 
</div>

Senior Executive Microbiologist

Prospect Medical Holdings, Inc.

<div>
 
 Job Description
 
 
 
 The Clinical Microbiologist Scientist (CMS) conducts a wide range of standardized and highly specialized microbiological analyses. They ensure the accuracy, reliability, and timely delivery of patient test results across all phases&mdash;pre-analytical, analytical, and post-analytical&mdash;which are critical for patient diagnosis, management, and treatment. Additionally, the Scientist supports effective communication by skillfully using computer and phone systems, fostering strong customer relationships, and consistently demonstrating professionalism, empathy, and respect toward all patients and colleagues.
 
 
 
 Responsibilities
 
 
 
 <ul>
 <li>
 The Clinical Microbiologist Scientist (CMS) is responsible for performing precise laboratory testing, implementing quality control measures, and ensuring the accurate and timely distribution of test results within the microbiology department. This role focuses on the identification of microorganisms and their clinical significance, rather than conducting a broad range of tests. The CMS strictly adheres to the laboratory&rsquo;s quality control policies, meticulously documenting all quality control activities, instrument calibrations, procedural adjustments, and maintenance performed to maintain the highest standards.
 </li>
 <li>
 Actively engages in continuous process improvement initiatives within the microbiology department to enhance workflow efficiency and test accuracy. Strictly adheres to turnaround time (TAT) guidelines for both STAT and routine microbiological tests to support timely patient diagnosis and treatment. Ensures full compliance with infection control protocols specific to microbiology, HIPAA regulations, and all other relevant regulatory standards to maintain a safe and confidential laboratory environment.
 </li>
 <li>
 Empathizes with patient and patient support systems, expresses compassion and understanding for the situation and demonstrates care, which is appropriate for the age, and cultural, religious, gender identity, or ethnic background. Engages in caring behaviors, taking conscious ownership for work and takes deliberate/thoughtful actions regarding how to best carry out interactions with the patient, families, physicians, and co-workers.
 </li>
 <li>
 Identifies and troubleshoots issues that could negatively impact test accuracy or the timely reporting of results, taking corrective action or promptly notifying the Director, Manager, or Supervisor as needed. This includes recognizing atypical microbial growth or contamination and swiftly collaborating with appropriate personnel to resolve these concerns. Maintains thorough documentation of all corrective actions taken whenever test systems deviate from the laboratory&rsquo;s established performance standards, ensuring traceability and quality assurance.
 </li>
 <li>
 Adheres strictly to the microbiology laboratory&rsquo;s protocols for the safe handling, storage, and proper disposal of specimens, reagents, and biohazardous waste to maintain a safe working environment and prevent contamination. Accurately performs microbiological tests, ensures precise reporting, and maintains comprehensive records of patient test results to support reliable diagnosis and treatment. Keeps detailed documentation demonstrating that proficiency testing samples are processed and analyzed with the same rigor and procedures as patient specimens to ensure consistent quality and compliance with regulatory standards.
 
 
 </li>
 </ul>
 
 Qualifications
 
 
 
 
 Southern Cali Hospital Culver City
 
 
 
 
 Required Qualifications:
 
 
 
 <ul>
 <li>
 Bachelor&rsquo;s degree in medical technology/clinical laboratory science/Biological Science or Equivalent
 </li>
 <li>
 Current Licensure as a Clinical Microbiologist Scientist (CMS) License or a CLS license with the experience applicable to microbiology in the State of California
 </li>
 <li>
 Ability to establish and maintain effective working relationships across the hospital
 </li>
 <li>
 Ability to maintain a work pace appropriate to the workload
 </li>
 <li>
 Excellent written and verbal communication skills in English
 </li>
 <li>
 Must be willing to work variable shifts and overtime as required
 </li>
 <li>
 Must demonstrate customer service skills appropriate to the job
 </li>
 <li>
 Ability to identify and distinguish colors
 
 
 </li>
 </ul>
 
 Preferred Qualifications:
 
 
 
 <ul>
 <li>
 Experience with lab/hospital computer systems and software
 </li>
 <li>
 Applicable prior experience in a clinical microbiology laboratory, including experience with various identification platforms and antimicrobial susceptibility testing methods.
 </li>
 <li>
 Bilingual skills to communicate effectively with patients and families
 
 
 </li>
 </ul>
 
 Pay Rate: Min - $53.55 | Max - $71.94
 
 
 
 
 About Us
 
 
 
 Southern California Hospital at Culver City has been taking care of generations of Culver City and west LA residents. We are a full-service, acute care hospital with a 24/7 emergency department and nationally recognized patient safety. Now at 420 beds, SCH-CC is a general acute care hospital that utilizes many of the latest medical treatments and technologies. The hospital offers a wide range of inpatient and outpatient acute care services, including an orthopedic center, cardiovascular services, acute rehabilitation, sub-acute care, psychiatric care and chemical dependency programs. Additionally, SCH-CC operates a 24-hour emergency services center, which serves as a paramedic receiving station and is staffed by board-certified emergency physicians and nurse specialists.
 
 
 
 Union Pay Info: https://www.pmh.com/schccunion-8hr/
 
</div>

Clinical Microbiologist Scientist - Part Time, Evening/Mid (Culver City)

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