quality control microbiologist

Prof Compounding Centers of America

<div>Position Summary

The Quality Control Microbiologist performs quality review activities supporting both sterile and non-sterile microbiological testing. This role is responsible for reviewing routine microbiology data, documentation, and quality investigations to ensure compliance with cGMP, cGLP, ISO 17025, A2LA, and USP requirements, as well as Eagle Analytical&rsquo;s Quality Management System. The position works closely with laboratory operations to maintain data integrity, regulatory compliance, and continuous improvement across microbiology testing functions.

What You Will Do
<ul>
<li>Ensure compliance with Eagle Analytical policies, Standard Operating Procedures (SOPs), and the Quality Management System.</li>
<li>Interpret and apply regulatory and accreditation standards, including ISO 17025, cGMP, cGLP, USP, and A2LA requirements.</li>
<li>Support regulatory inspections, client audits, and accreditation assessments as required.</li>
<li>Review microbiological test data and documentation related to sterility, endotoxin, bioburden, microbial limits, environmental monitoring, and particulate matter testing.</li>
<li>Verify data integrity, accuracy, completeness, and traceability for laboratory worksheets, logbooks, and reports.</li>
<li>Maintain accurate and compliant quality records and documentation.</li>
<li>Review and approve quality investigations, including Out-of-Specification (OOS), Nonconformance Reports (NCR), Deviations (DV), Corrective and Preventive Actions (CAPA), change controls, and customer complaints.</li>
<li>Evaluate root cause analyses and corrective action plans for laboratory and process-related issues.</li>
<li>Prepare audit finding reports and determine appropriate corrective and preventive actions.</li>
<li>Support and conduct internal audits of quality systems and microbiology laboratories.</li>
<li>Perform routine compliance walk-through audits to ensure ongoing adherence to regulatory and quality requirements.</li>
<li>Manage auditing, storage, retention, and control of quality documentation and quarantined materials.</li>
<li>Write, review, and approve SOPs, work instructions, forms, and quality records to ensure regulatory compliance and operational consistency.</li>
<li>Assist in creating and maintaining quality manuals, procedures, and controlled documentation.</li>
<li>Prepare and maintain quality-related training materials as assigned.</li>
<li>Communicate findings, trends, and risks with laboratory management and quality leadership.</li>
<li>Support continuous improvement initiatives related to quality systems, documentation, and laboratory compliance.</li>
<li>Perform additional duties and special projects as assigned to support quality and regulatory objectives.</li>
</ul>
Who You Are
<ul>
<li>Bachelor&rsquo;s degree in Microbiology, Biology, or a related life science required.</li>
<li>Experience in sterile and/or non-sterile microbiology testing preferred.</li>
<li>Knowledge of cleanroom practices and microbiological testing principles.</li>
<li>Experience working in a regulated laboratory environment (ISO 17025, cGMP, cGLP) preferred.</li>
<li>Experience reviewing GMP/GLP documentation and quality investigations preferred.</li>
<li>Strong attention to detail with a demonstrated commitment to data integrity and regulatory compliance.</li>
<li>Excellent written and verbal communication skills.</li>
<li>Ability to work independently while collaborating effectively with cross-functional teams.</li>
<li>Proficiency in Microsoft Office applications and electronic document management systems.</li>
<li>ASQ certification or related quality credentials preferred.</li>
</ul>
Who We Are

Serving customers since 2004, Eagle offers the highest quality in preparation testing for sterility, bacterial endotoxins, microbial detection, beyond-use dating (BUD) determination and active ingredient potency. State-of-the-art equipment, combined with the experience and knowledge of our team, makes Eagle the best choice for all testing needs. The Eagle team is committed not only to performing the best quality control testing, but also working relentlessly with our customers on solutions if tests receive unexpected results. Learn more at www.eagleanalytical.com.<h4 class="jobSectionHeader">
Education</h4>
Preferred<ul><li>
Bachelors or better in Microbiology and Molecular Cell Sciences or related field</li><li>
Bachelors or better in Microbiology or related field</li><li>
Bachelors or better in Biology or related field</li><li>
Bachelors or better in Biochemistry or related field</li></ul><h4 class="jobSectionHeader">
Behaviors</h4>
Preferred<ul><li>
Team Player: Works well as a member of a group</li><li>
Dedicated: Devoted to a task or purpose with loyalty or integrity</li><li>
Detail Oriented: Capable of carrying out a given task with all details necessary to get the task done well</li></ul><h4 class="jobSectionHeader">
Motivations</h4>
Preferred<ul><li>
Goal Completion: Inspired to perform well by the completion of tasks</li><li>
Self-Starter: Inspired to perform without outside help</li></ul>
Equal Opportunity Employer 
This employer is required to notify all applicants of their rights pursuant to federal employment laws. For further information, please review the Know Your Rights notice from the Department of Labor.</div>

Quality Control Microbiologist

Cosmo Pharma Int. Pvt. Ltd

We are looking for a MicrobiologistExperience: 2 &ndash; 4 years with medical/Pharma companies.Location: Karachi/Azizabad site f.b AreaJob responsibilities but not limited to:<ul><li>Responsible for testing and analysis as per documented procedures/methods for the product.</li></ul><ul><li>Compilation and reporting of analysis and results.</li></ul><ul><li>Calibration of equipment&rsquo;s and instruments as per SOP in microbiology.</li></ul><ul><li>Performing laboratory analysis on all materials after appropriate sterilization.</li></ul><ul><li>Performing tests on all incoming ingredients and documents all records.</li></ul><ul><li>Developing and preparing documents for all protocols.</li></ul><ul><li>Developing and documenting various microbiology laboratory processes and preparing final reports.</li></ul><ul><li>Conducting quality control tests. Testing quality of materials or finished products.</li></ul><ul><li>Maintaining laboratory instruments to ensure proper working order and troubleshooting malfunctions when needed. Education: Bachelors/Master&rsquo;s in Microbiology</li></ul>Timing: 09.00 AM to 06:00 PMJob Type: Full-timePay: From Rs35,000.00 per monthAbility to commute/relocate:<ul><li>Karachi: Reliably commute or planning to relocate before starting work (Required)</li></ul>Work Location: In person

Microbiologist

Nestlé

<div>Main Purpose of Job
You will be responsible for quality control microbiology testing of product materials and purified water as well as performing environmental monitoring. 
Responsibilities:<ul><li>
Perform and document in-house microbiological testing on raw materials, semi-finish, and finish product according to the established standard operating procedures and approved protocols.</li><li>
Prepare necessary standards, solutions, reagents, media, and samples for sample analysis.</li><li>
Accurately record observations and perform data reviews and release inspection lot in the material management system.</li><li>
Operates and maintains laboratory instruments, while ensuring the reliability of instrumentation through proper maintenance, with ability to troubleshoot minor issues.</li><li>
Must participate and lead continuous improvement using lean principles to assist with streamlining and making the laboratory efficient.</li><li>
Handling all paper works such as Reports.</li><li>
Prepare check receiving reports according to the accurate specs.</li><li>
Reporting of abnormalities via notification of quality deviations and take immediate corrections.</li><li>
Adhere to the Nestle SHE rules and procedures at all times during the working hours to ensure own and others safety.</li></ul>
Requirements:<ul><li>
Bachelor&rsquo;s degree on Microbiology or related major.</li><li>
 More than 1 year of experience in the same position.</li></ul> 
Skills:<ul><li>
Good math's and English skills.</li><li>
proficient in relevant computer applications such as MS Office.</li><li>
Accurate and organize.</li><li>
Ability to work under pressure.</li></ul></div>

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>

Sr. Microbiogy Specialist

Staq Pharma

<div><h3 class="jobSectionHeader">Company Overview &ndash; STAQ Pharma</h3>
STAQ Pharma is an FDA-registered 503B outsourcing facility dedicated to producing high-quality, sterile injectable medications for both adult and pediatric patients. All products are compounded under Current Good Manufacturing Practices (cGMP) standards.<ul><li>
Headquartered in Denver, Colorado with an additional facility in Columbus, Ohio</li><li>
Regulated by the FDA, DEA, and State Boards of Pharmacy</li><li>
Committed to Safety, Transparency, Availability, and Quality</li><li>
Equipped with state-of-the-art facilities and advanced automation to support the preparation of ready-to-administer pharmaceuticals (syringes, pumps, bags, etc.)</li></ul><h3 class="jobSectionHeader">
Position Summary</h3>
The Quality Control Microbiology Technician supports STAQ Pharma&rsquo;s environmental monitoring program and ensures compliance with cGMP standards and internal procedures. This role plays a key part in maintaining the integrity of cleanroom operations and supporting microbiological testing efforts across the facility.
Schedule: Monday to Friday, 2pm-10:30pm 
However, in the event of a production delay, the employee is expected to remain on-site to support operations until production is complete.<h3 class="jobSectionHeader">
Key Responsibilities</h3><ul><li>
Conduct viable and non-viable environmental monitoring (EM) of all classified cleanroom areas</li><li>
Perform surface sampling, active air, and passive air sampling according to SOPs</li><li>
Incubate and enumerate environmental monitoring samples</li><li>
Conduct morphology assessments following incubation</li><li>
Perform microbiological testing including gram stains, subculturing, and microorganism identification</li><li>
Maintain and monitor EM equipment (viable and non-viable samplers) for proper function</li><li>
Follow proper gowning and hygiene procedures to prevent contamination</li><li>
Work cross-functionally with production teams to resolve quality concerns and ensure complete, compliant documentation</li><li>
Support investigations related to environmental monitoring deviations or other quality issues</li><li>
Assist with continuous improvement initiatives within the EM program</li><li>
Submit and manage samples for third-party microbiological testing</li><li>
Participate in procedural reviews, equipment troubleshooting, and SOP revisions</li><li>
Perform other duties as assigned</li></ul><h3 class="jobSectionHeader">
Qualifications</h3>
Education:<ul><li>
Bachelor&rsquo;s degree in Microbiology or a closely related scientific field</li></ul>
Required Skills &amp; Competencies:<ul><li>
Strong organizational and communication skills</li><li>
Ability to follow strict cGMP and aseptic techniques</li><li>
Strong attention to detail</li></ul>
Preferred Experience:<ul><li>
Prior experience in a cGMP-regulated aseptic manufacturing environment</li><li>
Pharmaceutical or biotechnology industry background</li><li>
Familiarity with 21 CFR Part 11, 210, and 211 regulations</li><li>
Proficient in Microsoft Office (Word, Excel, PowerPoint, Outlook)</li><li>
Comfortable working in a fast-paced, dynamic environment with shifting priorities</li></ul><h3 class="jobSectionHeader">
Additional Notes</h3>
This position works closely with Operations and Quality leadership to support microbiological data collection and reporting efforts.</div>

Quality Control Microbiology Technician

Primary Responsibilities:<ul><li>controlling the quality of raw materials,</li><li>Build and maintain strong relationships with farmers, suppliers, and vendors.</li><li>Ensure procurement standards, quality checks, and compliance procedures.</li><li>frequent travel is a core part of the job.</li><li>Monitor market trends, pricing, and supply availability.</li></ul>Minimum Qualifications<ul><li>Bachelor s Degree in Microbiology, aquaculture Food Microbiology or related field, required.</li><li>6+ years full-time experience required. Experience in sea food industry is preferred.</li><li>Knowledge in food safety programs and regulations are plus.</li><li>Good verbal and written communication skills.</li><li>Proficiency with Microsoft Office tools.</li></ul>Job Type: Full-timePay: ₹20,000.00 - ₹25,000.00 per monthBenefits:<ul><li>Provident Fund</li></ul>Experience:<ul><li>Microbiologist: 3 years (Required)</li></ul>Work Location: In person

purchase manager for export to usa only

Regenix Drugs Ltd

Opening For Consultant Microbiologist (Diagnostic Work Experience Must)Qualification: P.HD MicrobiologyExperience: 7 to 10 YearsSalary: 45000 to 50000Location : ChennaiRoles &amp; Responsibilities:Consultant Microbiologist has to oversee the management and running of a Microbiology department and its staff. In many roles, you will also work alongside with technicians. In Microbiology and Molecular biology you will be mostly lab-based. Although specific tasks vary according to your specialty, there are some responsibilities common to all specialities and you'll typically need to:<ul><li>Examine and talk using diagnostic skills to determine what tests need to be carried out</li><li>Support and advise clinical staff to help them choose the correct tests</li><li>Work alongside biomedical scientists while they complete laboratory tests</li><li>Educate colleagues in the use and limitations of each diagnostic investigation</li><li>Provide advice and interpretation of test results and the appropriateness of further investigations</li><li>Undertake managerial responsibilities, such as planning the workload and staffing of the department, especially at more senior levels</li><li>Supervise and teach junior staff, depending on your post</li><li>Carry out research and keep up to date with new information relevant to your field.</li><li>Authorised signatory for release of Test Report</li></ul>Job Type: PermanentPay: ₹40,000.00 - ₹45,000.00 per monthBenefits:<ul><li>Provident Fund</li></ul>Work Location: In person

Opening For Consultant Microbiologist (Diagnostic Work Experience Must)

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