quality control microbiologist

CALO

<div>About Calo
Launched in Bahrain in November of 2019, Calo is on a mission to make healthy easy. We&rsquo;re a team of dedicated people driving this mission by providing better, faster, and cheaper ways to access food through technology.
Role overview<div>
We are looking for a Microbiologist who will be responsible for ensuring the microbiological safety and quality of all meal kit components and finished products. This role involves developing, implementing, and executing microbiological testing programs, conducting environmental monitoring, and performing root cause analysis to prevent and resolve potential contamination issues. The Microbiologist will play a critical role in supporting the company's commitment to delivering safe, fresh, and high-quality meals to our customers. 
Key Responsibilities:<ul><li>
Microbiological Testing:<ul><li>
Perform a variety of microbiological analyses on a routine basis, including testing raw materials, in-process samples (e.g., prepared sauces, fresh cuts), and finished meal.</li><li>
Test for a range of microorganisms, including pathogens (e.g., Listeria, Salmonella, E. coli) and indicator organisms (e.g., total plate count, yeast and mold, coliforms).</li><li>
Conduct shelf-life studies and challenge tests to validate product freshness and safety.</li><li>
Utilize and maintain laboratory equipment such as incubators, autoclaves, and rapid pathogen detection systems.</li></ul></li><li>
Environmental/Pathogen Monitoring Program (EMP):<ul><li>
Develop and execute a comprehensive environmental monitoring program for all food preparation and packaging areas.</li><li>
Collect and analyze swabs from food contact surfaces, non-food contact surfaces, and the general environment.</li><li>
Identify potential harborage sites for pathogens and recommend corrective actions to prevent microbial growth.</li></ul></li><li>
Data Analysis and Reporting:<ul><li>
Accurately record, analyze, and interpret all microbiological data.</li><li>
Prepare and present technical reports on test results, trends, and findings to the Food Safety and Quality Manager and other cross-functional teams.</li><li>
Assist in the development and maintenance of a robust data management system for all microbiological information.</li></ul></li><li>
Problem-Solving and Investigation:<ul><li>
Lead or support investigations into out-of-specification results or customer complaints related to microbial contamination.</li><li>
Conduct root cause analysis to identify the source of contamination and implement effective corrective and preventative actions.</li><li>
Collaborate with the production, culinary, and supply chain teams to troubleshoot issues and improve processes.</li></ul></li><li>
Compliance and Documentation:<ul><li>
Ensure all laboratory procedures and documentation adhere to established SOPs, GMPs, and regulatory standards (e.g., SFDA, HACCP).</li><li>
Stay current with the latest food safety regulations, testing methodologies, and industry best practices.</li><li>
Assist in preparing for and participating in all internal, third-party, and regulatory audits.</li></ul></li></ul>
Ideal Candidate
Qualifications<ul><li>
Bachelor&rsquo;s degree in Microbiology and Chemistry.</li><li>
Minimum of 3 years of experience in a food microbiology laboratory, preferably within a high-volume food production, RTE meals, or food service environment</li><li>
Must be based in Saudi Arabia</li></ul>
Knowledge and Competency<ul><li>
Proficient in GLP, aseptic techniques, and microbiological laboratory procedures.</li><li>
Skilled in pathogen detection methods (e.g., PCR, ELISA), rapid testing, and traditional plating techniques.</li><li>
Solid understanding of HACCP principles and food safety regulations.</li><li>
Excellent analytical, decision-making, and problem-solving skills.</li><li>
Great attention to detail with a results-driven approach.</li><li>
Excellent written and verbal communication skills in English.</li><li>
Able to promote and uphold a strong food safety culture.</li><li>
Adaptable, fast learner, and able to manage multiple tasks in a fast-paced environment.</li></ul>
Personality<ul><li>
Reliable, trustworthy, and committed to laboratory safety and food safety protocols.</li><li>
Pleasant personality with the ability to collaborate and communicate effectively across teams.</li></ul></div>
w1QAlPKlkV</div>

Microbiologist

FujiFilm

<div>Position Overview:

The Microbiologist I will be responsible for assisting the QC microbiological aspects of cGMP compliance and testing at the FUJIFILM Biotechnologies Texas Quality Control Laboratory. 
Company Overview:

The work we do at FUJIFILM Biotechnologies Texas has never been more important&mdash;and we are looking for passionate, mission-driven people like you who want to make a real difference in people&rsquo;s lives. 
 
From developing the next vaccine to advancing cell and gene therapies, we collaborate with industry leaders to tackle complex challenges and deliver meaningful solutions. 
 
If you&rsquo;re ready to help transform the future of medicine, join FUJIFILM Biotechnologies. We offer a flexible work environment and we&rsquo;re proud to cultivate a culture that will fuel your passion, energy, and drive&mdash;what we call Genki. 
 
Our state-of-the-art biomanufacturing facility is located in in College Station, Texas, which combines a small-town feel with vibrant culture, top-notch schools, and close proximity to big city life. Nestled between major hubs, it&rsquo;s a dynamic location that blends convenience with innovation. 
 
Fujifilm is globally headquartered in Tokyo with over 70,000 employees across four key business segments of healthcare, electronics, business innovation, and imaging. We are guided and united by our Group Purpose of &ldquo;giving our world more smiles.&rdquo; Visit: https://www.fujifilm.com/us/en/about/region/careers
Job Description:

Primary Responsibilities:<ul><li>
Collect environmental monitoring (Total Air, Viable Air and Viable Surface) in a cleanroom/controlled environment.</li><li>
Collect Utility Monitoring Samples (RODI/WFI) routinely and for qualification of systems.</li><li>
Sample Compressed Gas/Process Gas system.</li><li>
Autoclave materials and components for use in the QC laboratory.</li><li>
Routine QC laboratory cleaning</li><li>
Management of inventory items for the laboratory</li><li>
Ensure the lab is maintained (organized, clean, &amp; properly supplied).</li><li>
Perform other duties as assigned.</li></ul><div>
Qualifications:
</div><ul><li>Associate&rsquo;s degree preferably in Biochemistry, Chemistry, Biology, or related field; OR,</li><li>
High School Diploma or GED and 1+ year of relevant experience.</li><li>
Ability to analyze raw data, assess assay and system suitability criteria.
</li><li>Ability to follow safety procedures outlined in the Chemical Hygiene Plan.</li><li>
Utilize SDS sheets to properly assess chemical hazards, spill response procedures, and PPE requirements if indicated.</li><li>
Good attention to detail and ability to utilize problem solving/trouble shooting skills.</li><li>
Good computer skills.</li><li>
Demonstrated written and oral communication skills.</li><li>
Strong organization and analytical skills.</li><li>
Role model for company core values of trust, delighting our customers, Gemba, and Genki.</li></ul><div>
Physical Requirements:</div>
The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee is regularly required to:<ul><li>
Experience prolonged standing, some bending, stooping, and stretching.</li><li>
Use hand-eye coordination and manual dexterity sufficient to operate a keyboard, photocopier, telephone, calculator, and other office equipment is required.</li><li>
Ability to sit for long periods to work on a computer.</li><li>
Potential for exposure to hazardous chemicals, gases, fumes, odors, mists, and dusts, and other hazardous materials.</li><li>
Ability to lift/pull/push 50 lbs on occasion and 15 lbs regularly.</li><li>
Ability to wear personal protective equipment including safety glasses, lab coat, and gloves.
</li><li>Attendance is mandatory.</li></ul><div>
Join us! FDB is advancing tomorrow&rsquo;s medicine, impassioning employees to chase the impossible and continually expand their potential. We are a company of emboldened goal seekers &ndash; driven by an innate desire to better ourselves, our families, our workplace, our company, our community and the world at large.</div><div> 
To all agencies: Please, no phone calls or emails to any employee of FUJIFILM about this requisition. All resumes submitted by search firms/employment agencies to any employee at FUJIFILM via-email, the internet or in any form and/or method will be deemed the sole property of FUJIFILM, unless such search firms/employment agencies were engaged by FUJIFILM for this requisition and a valid agreement with FUJIFILM is in place. In the event a candidate who was submitted outside of the FUJIFILM agency engagement process is hired, no fee or payment of any kind will be paid.</div> 
<div></div>
EEO Information:
<div>
Fujifilm is committed to providing equal opportunities in hiring, promotion and advancement, compensation, benefits, and training regardless of nationality, age, gender, sexual orientation or gender identity, race, ethnicity, religion, political creed, ideology, national, or social origin, disability, veteran status, etc.</div>
ADA Information:
<div>
If you require reasonable accommodation in completing this application, interviewing, completing any pre-employment testing, or otherwise participating in the employee selection process, please direct your inquiries to our HR Department (FDBTHR@fujifilm.com or (979) 431-3500).</div></div>

QC Analyst I, Microbiology

Sandoz

<div>
 
 
 Job Description
 
 
 
 
 
 Major accountabilities:
 
 
 
 <ul>
 <li>
 OOx/Deviation handling.
 </li>
 <li>
 CAPA definition -KPI trending -Ensure all activities in compliance with cGxP, incl. data integrity review and approval of analytical data / tests (analytical release) Stability -Stability testing (Projects) &ndash; protocol preparation, evaluation, report preparation.
 </li>
 <li>
 Reporting (Stability plan preparation, trend analysis, evaluation)
 </li>
 <li>
 Performance of Stability studies, protocols and comparative reports for supplier qualification -Review and approval of analytical tests (analytical release)
 </li>
 <li>
 Microbiological QC -Perform Microbiological testing of materials and utilities, environmental and personnel monitoring -Provide expert Support for site qualification and validation activities -Maintain and calibrate equipment incl. plan preparation -Support in supplier qualification -Trending and analysis of KPI/KQI -Support sample planning and sampling execution -Reporting of technical complaints / adverse events / special case scenarios related to Sandoz products within 24 hours of receipt -Distribution of marketing samples (where applicable)
 
 
 </li>
 </ul>
 
 
 Job Description:
 
 
 
 
 <ul>
 <li>
 To prepare, update, and track revisions of laboratory procedures in accordance with current and legal regulatory guidelines.
 </li>
 <li>
 To work in compliance with current GMP rules and company procedures.
 </li>
 <li>
 To conduct and report necessary activities within the quality management system (OOS/OOT, Deviation Investigation, Change Control, and Corrective and Preventive Actions).
 </li>
 <li>
 To perform and report microbiological analyses of raw materials, semi-finished products, finished products, and packaging materials.
 </li>
 <li>
 To carry out and report the microbiological method validation and verification studies.
 </li>
 <li>
 To implement the environmental monitoring program, evaluate results, and report findings.
 </li>
 <li>
 To perform and evaluate the microbiological controls of compressed air systems.
 </li>
 <li>
 To perform and evaluate microbiological analyses of the water system.
 </li>
 <li>
 To perform microbiological analyses of detergents and disinfectants used.
 </li>
 <li>
 To perform, evaluate, and report disinfectant efficacy studies in accordance with pharmacopeia and related standards.
 </li>
 <li>
 To prepare all culture media and solutions used in the laboratory according to instructions and to perform growth promotion studies.
 </li>
 <li>
 To prepare for and participate in customer and regulatory audits.
 </li>
 <li>
 To conduct and report Microbiological Risk Assessments and OPEX studies.
 </li>
 <li>
 To perform bulk holding time (BHT) studies, evaluate results, and report findings.
 </li>
 <li>
 To ensure the calibration and verification of used equipment are carried out and tracked.
 </li>
 <li>
 To support the qualification and calibration processes of laboratory equipment.
 </li>
 <li>
 To ensure the regular and effective operation of the microbiology laboratory.
 </li>
 <li>
 To ensure the preparation of periodic trend reports and their timely implementation.
 </li>
 <li>
 To ensure that laboratory records are accurate and complete.
 </li>
 <li>
 To track, prepare, and report reference cultures of microorganisms.
 </li>
 <li>
 To perform and report microorganism identifications.
 
 
 </li>
 </ul>
 
 
 Key Performance Indicators:
 
 
 
 
 <ul>
 <li>
 The relevant KPIs that are defined in the Quality Control areas apply: e.g. analytical lead times -Timely and GMP-compliant analysis &amp; documentation of the results.
 </li>
 <li>
 Error rate: Number of OOS (analysis errors) related to the number of analyzes -No complaints about official inspections.
 </li>
 <li>
 Individual performance is assessed using the PMP performance dialog together with the manager
 
 
 </li>
 </ul>
 
 Minimum Requirements:
 
 
 Work Experience:
 
 
 
 <ul>
 <li>
 Functional Breadth.
 </li>
 <li>
 Preferably at least 4 years of experience in a microbiology laboratory, particularly in the pharmaceutical industry (especially in non-sterile manufacturing).
 </li>
 <li>
 Collaborating across boundaries.
 </li>
 <li>
 A GMP environment/equivalent.
 </li>
 <li>
 Bachelor&rsquo;s degree in Microbiology, Biology, Molecular Biology &amp; Genetics, or Bioengineering from the university.
 </li>
 <li>
 Good command of English (reading, writing, speaking).
 </li>
 <li>
 Knowledge and experience in microbiological analysis techniques (e.g., disinfectant efficacy studies, non-sterile product analysis tests, etc.).
 </li>
 <li>
 Proficiency in MS Office programs.
 
 
 </li>
 </ul>
 
 
 Skills:
 
 
 
 
 <ul>
 <li>
 Continuous Learning.
 </li>
 <li>
 Dealing With Ambiguity.
 </li>
 <li>
 Decision Making Skills.
 </li>
 <li>
 Gxp.
 </li>
 <li>
 Industry Standards.
 </li>
 <li>
 Laboratory Equipment.
 </li>
 <li>
 Laboratory Excellence.
 </li>
 <li>
 Quality Control (QC) Testing.
 </li>
 <li>
 Quality Control Sampling.
 </li>
 <li>
 Self-Awareness.
 </li>
 <li>
 Technological Expertise.
 </li>
 <li>
 Total Quality Management.
 </li>
 <li>
 Team-oriented, with strong communication skills, responsible, and detail-oriented.
 </li>
 <li>
 Possesses problem-solving and analytical thinking skills.
 </li>
 <li>
 Able to keep up with the busy work tempo
 
 
 </li>
 </ul>
 
 
 Languages:
 
 
 
 
 <ul>
 <li>
 English.
 </li>
 </ul>
</div>

Microbiogy Specialist

<div>Major accountabilities:
<ul><li>OOx/Deviation handling.
</li><li>CAPA definition -KPI trending -Ensure all activities in compliance with cGxP, incl. data integrity review and approval of analytical data / tests (analytical release) Stability -Stability testing (Projects) &ndash; protocol preparation, evaluation, report preparation.
</li><li>Reporting (Stability plan preparation, trend analysis, evaluation)
</li><li>Performance of Stability studies, protocols and comparative reports for supplier qualification -Review and approval of analytical tests (analytical release)
</li><li>Microbiological QC -Perform Microbiological testing of materials and utilities, environmental and personnel monitoring -Provide expert Support for site qualification and validation activities -Maintain and calibrate equipment incl. plan preparation -Support in supplier qualification -Trending and analysis of KPI/KQI -Support sample planning and sampling execution -Reporting of technical complaints / adverse events / special case scenarios related to Sandoz products within 24 hours of receipt -Distribution of marketing samples (where applicable) 
</li></ul>Job Description:
<ul><li>To prepare, update, and track revisions of laboratory procedures in accordance with current and legal regulatory guidelines.
</li></ul>&middot; To work in compliance with current GMP rules and company procedures.
&middot; To conduct and report necessary activities within the quality management system (OOS/OOT, Deviation Investigation, Change Control, and Corrective and Preventive Actions).
&middot; To perform and report microbiological analyses of raw materials, semi-finished products, finished products, and packaging materials.
&middot; To carry out and report the microbiological method validation and verification studies.
&middot; To implement the environmental monitoring program, evaluate results, and report findings.
&middot; To perform and evaluate the microbiological controls of compressed air systems.
&middot; To perform and evaluate microbiological analyses of the water system.
&middot; To perform microbiological analyses of detergents and disinfectants used.
&middot; To perform, evaluate, and report disinfectant efficacy studies in accordance with pharmacopeia and related standards.
&middot; To prepare all culture media and solutions used in the laboratory according to instructions and to perform growth promotion studies.
&middot; To prepare for and participate in customer and regulatory audits.
&middot; To conduct and report Microbiological Risk Assessments and OPEX studies.
&middot; To perform bulk holding time (BHT) studies, evaluate results, and report findings.
&middot; To ensure the calibration and verification of used equipment are carried out and tracked.
&middot; To support the qualification and calibration processes of laboratory equipment.
&middot; To ensure the regular and effective operation of the microbiology laboratory.
&middot; To ensure the preparation of periodic trend reports and their timely implementation.
&middot; To ensure that laboratory records are accurate and complete.
&middot; To track, prepare, and report reference cultures of microorganisms.
&middot; To perform and report microorganism identifications.
Key performance indicators:
<ul><li>The relevant KPIs that are defined in the Quality Control areas apply: e.g. analytical lead times -Timely and GMP-compliant analysis &amp; documentation of the results.
</li><li>Error rate: Number of OOS (analysis errors) related to the number of analyzes -No complaints about official inspections.
</li><li>Individual performance is assessed using the PMP performance dialog together with the manager
</li></ul>Minimum Requirements:
 
Work Experience:
<ul><li>Functional Breadth.
</li><li>Preferably at least 4 years of experience in a microbiology laboratory, particularly in the pharmaceutical industry (especially in non-sterile manufacturing).
</li><li>Collaborating across boundaries.
</li><li>A GMP environment/equivalent.
</li><li>Bachelor&rsquo;s degree in Microbiology, Biology, Molecular Biology &amp; Genetics, or Bioengineering from the university. 
</li></ul><ul><li>Good command of English (reading, writing, speaking).
</li><li>Knowledge and experience in microbiological analysis techniques (e.g., disinfectant efficacy studies, non-sterile product analysis tests, etc.).
</li><li>Proficiency in MS Office programs.
</li></ul>Skills:
<ul><li>Continuous Learning.
</li><li>Dealing With Ambiguity.
</li><li>Decision Making Skills.
</li><li>Gxp.
</li><li>Industry Standards.
</li><li>Laboratory Equipment.
</li><li>Laboratory Excellence.
</li><li>Quality Control (QC) Testing.
</li><li>Quality Control Sampling.
</li><li>Self-Awareness.
</li><li>Technological Expertise.
</li><li>Total Quality Management.
</li><li>Team-oriented, with strong communication skills, responsible, and detail-oriented.
</li></ul>&middot; Possesses problem-solving and analytical thinking skills.
<ul><li>Able to keep up with the busy work tempo
</li></ul>Languages:
<ul><li>English.</li></ul></div>

QC Microbiology Specialist

WMF's Villoo Poonawalla Memorial Hospital

Operational1. Collects the data on Nosocomial infections through daily surveillance and culture reports.2. Make regular visit to the clinical area to make sure that the patients with particular infection receives an appropriate treatment in regard to the isolation precaution, and the type of treatment that the patient has to receive.3. Make sure that; the staffs are educated and updated with the protocols in relation to the infection control.4. Advise and supervise the work of staff. Arrange special teaching session to the staff and even for specific group of patients pertaining to the infection control and prevention.5. Collect data of patients with infections that require isolation precaution and use of specific antibiotics e.g. MRSA.6. Conduct clinical audit to make sure that, the high standard of care in place in relation to the infection control and prevention.7. Update self-knowledge by participating in the clinical governance meeting.8. Cascade the updated information to the infection control link nurses of the hospital.9. Share her or his concern or worries to the Infection control consultant/ microbiologist in order to get an idea and for a possible solution.10. In the hospital situation, any outbreak of infection is normally informed by the Head of the microbiology or virology department. The information will then be cascaded to the Hospital/ ward through the infection control nurses and infection control link nurses.11. The Infection Control Nurse will act as a resource person to staff around specific infection control issues concerning specific patients or groups of patients.12. The ICN will be responsible for reviewing and updating infection control policies in conjunction with the Infection Control Officer (Microbiologist).13. Should be self-directed and responsible for completing all required documentation.14. Work with team members in order to ensure effective communication of the changing infection control needs.15. Communicate infection control principles in a concrete manner that is appropriate for all health care workers.16. Be a member secretary of Infection Control CommitteeJob Type: Full-timePay: &#8377;25,000.00 - &#8377;40,000.00 per monthApplication Question(s):<ul><li>Candidate must have at least 1 year of experience of working as Infection Control Nurse with NABH certified hospital.</li></ul>Work Location: In person

Infection Control Nurse

Western India Cashew Company Pvt Ltd

Job descriptionIndustry - FMCG / Foods / BeverageCategory - MicrobiologistJob Type - PermanentJob Description :- The role is responsible for undertaking Supplier Quality Assurance (SQA) process with suppliers to ensure the evaluation and upgradation of a supplier's capability to meet company standards and coordinating with suppliers for resolution of non-conforming quality issues.Client DetailsLeading FMCG company with operations in more than countries and frequently rated as one of the Top Exporting companies to work for.Description<ul><li>- Conducting the Quality &amp; Food Safety (Q&amp;FS) audits for the suppliers facilities to meet company's standards and also benchmarking their capability as per the internal guidelines.</li><li>- Collaborating with the suppliers to ensure adherence to Average Service Level (ASL) as set by the global leadership.</li><li>- Supporting the suppliers to probe and prepare an action plan to resolve non-conformance.</li><li>- Ensuring constant upgradation and development of supplier base to meet future requirement.</li><li>- Ensuring the quality controls are working effectively throughout the supply chain.</li><li>- Interacting extensively with internal customers and suppliers.</li></ul>ProfileA successful candidate should have:- A bachelors degree with a minimum of2 years of experience working in F&amp;B sector.- Hands on experience working with SQA team in Food &amp; Beverages.- Extensive experience working with auditing systems, statistical evaluation, customer certifications, etc.- Ability to collaborate extensively with multiple stakeholders including but not limited to internal customers and suppliers.- Excellent communication skills as role involves substantial interactions with regional leadership.Job Type: Full-timeQualification: MicrobiologistBenefits:<ul><li>Provident Fund</li></ul>Schedule:<ul><li>Day shift</li></ul>Job Type: Full-timeBenefits:<ul><li>Provident Fund</li></ul>Education:<ul><li>Master's (Preferred)</li></ul>Experience:<ul><li>QC: 2 years (Preferred)</li></ul>Location:<ul><li>Karunagappalli, Kerala (Required)</li></ul>Work Location: In person

Quality Controller FMCG / Foods / Beverage Category

Search 10000+ Quality control microbiologist jobs near you this November. New roles added regularly across leading industries. Apply today.

10000 quality control microbiologist jobs NEAR_ME

Microbiologist

QC Analyst I, Microbiology

Microbiogy Specialist

Microbiogy Specialist

QC Microbiology Specialist

Infection Control Nurse

Quality Controller FMCG / Foods / Beverage Category