microbiology consultant

Austin Allen Company, LLC

<BR><p><strong>Sanitation Manager 3 rd Shift</strong></p><BR><p> </p><BR><p><strong>Salary Up to $110,000 plus Bonus, Benefits & Relocation Package to Midwest USA</strong></p><BR><p><strong> </strong></p><BR><p>One of the leading food manufacturers in the USA is searching for a Sanitation Manager for one of their growing plants. As the Sanitation Manager, you will support and provide instruction, training, and education to operations and quality assurance in the areas of sanitation and food safety. Youll develop effective relationships to function as a principal internal consultant for sanitation related food safety risk mitigation and adverse event management. You will also provide sanitation systems gap assessments and audits in operations (link removed) Must be a leader with food manufacturing and sanitation.</p><BR><p><strong> </strong></p><BR><p><strong>Minimum requirements for this Sanitation Managers position:</strong></p><BR><ul><BR><li>Bachelor of Science in food science, food safety, food technology, food engineering, or a related science discipline such as biology, microbiology, or chemistry</li><BR></ul><BR><ul><BR><li>Minimum of 6 years of Sanitation Leadership</li><BR><li>Experience monitoring & controlling environmental pathogens & allergens</li><BR><li>Pest Control experience to include stored product pest management. </li><BR></ul><BR><img src="https://www.jobg8.com/Tracking.aspx?Uchc6f7e1KEITbdtMJIqFJ82IiycwBd3y" width="0" height="0" />

Sanitation Manager 3rd Shift

Vivid Healthcare Search Limited

<p>Vivid Healthcare are looking for an experienced Band 4 AP Locum within Histology in Essex</p><p>Pay: £13- 20 per hour</p><p>Position Details: Microtomy experience, minimum 20 blocks per hour</p><p>Start Date: ASAP</p><p>Location: Essex</p><p>Duration: Ongoing</p><p>Essential: HCPC Registration</p><p>Registering with Vivid Healthcare comes with extensive benefits:</p><p></p><p>Full online and Practical Trainings</p><p>First refusals on all locum positions prior to being advertised.</p><p>CPD re-reimbursements (Terms and Conditions Apply)</p><p>Experienced Consultant (one point of contact)</p><p>Online timesheets where you can log in at any time and print your weekly income.</p><p>Contactable at any time/nights/weekends</p><p></p><p>To be successful for this role, you must be a fully qualified BMS with a minimum of 12 months recent experience within a UK based hospital and proven experience within Microbiology.</p><p>We offer a £250 referral bonus on successful placement (terms and qualifying period apply). Should this position not be of interest we have a number of roles around the UK offering great packages, please call the BMS team if you would like to know more information.</p><img src="https://www.jobg8.com/Tracking.aspx?b3tFgLThzreCe%2bAX9x85%2bY8VkITPGjSUe" width="0" height="0" />

Band 4 Histology AP (BMS) Locum Essex

VNR Seeds

<div></div><div><div><div><div><div><div>Job Code</div> <div>VSPL/BS/Lab Assistant Pathology/809-2025
</div></div><br>
<div><div>Job Category</div> <div>Breeding Support
</div></div><br>
<div><div>Job Description</div>
<div><ul><li>To assist in day-to-day laboratory activities related to plant pathology, microbiology, and biotechnology.</li>
</ul>
<p><b>Key Responsibilities:</b></p>
<ul> <li>Disease sample collection, isolation, subculture and maintenance/storage of pathogens as per SOPs.</li>
<li>Media preparation for culturing plant pathogens and inoculum preparation for greenhouse disease evaluations and for use in lab experiments.</li>
<li>Assist scientists in conducting research experiments and tests on plant diseases.</li>
<li>Laboratory maintenance, ensure all glassware and equipment are properly sanitized and sterilized and safety of laboratory equipments.</li>
<li>Maintain inventory of lab supplies, reagents and chemicals.</li>
<li>Strict adherence to all laboratory safety policies and procedures, including the proper handling and disposal of bio-hazardous waste.</li>
<li>Record keeping and report generation - document all laboratory procedures, test results, and observations and to assist scientists in compiling data findings into reports, summaries.</li>
</ul>
<p><b>Skills &amp; Competencies:</b></p>
<ul><li>Basic knowledge of laboratory equipment and microbiological techniques.</li>
<li>Attention to detail and accuracy in recording observations.</li>
<li>Good communication and teamwork skills.</li>
<li>Familiarity with MS Excel / basic computer operation.</li>
<li>Willingness to work in a research farm/lab environment.</li>
</ul></div>
</div><br>
<div><div>Desired Candidate Profile</div>
</div><br>
<div></div><div><div>Education Qualification</div>
<div><ul><li>Bachelor of Science - Biology
</li><li>Bachelor of Science - Botany
</li><li>Bachelor of Science - Microbiology
</li><li>Master of Science - Biology
</li><li>Master of Science - Botany
</li><li>Master of Science - Microbiology
</li></ul></div></div><br>
<div><div>Work Experience</div> <div>B.Sc. (Science &ndash; Biology / Botany / Microbiology) with 1&ndash;2 years of experience in a microbiological or pathology lab. OR M.Sc. (Science &ndash; Biology / Botany / Microbiology) &ndash; Fresher can apply.</div>
</div><br>
<div><div>Job Location</div> <div>Bemetara ( Chhattisgarh )
</div></div><br>
<div><div>Salary Package</div> <div>Best as per industry standards</div></div></div></div></div></div><p></p>

Lab Assistant Pathology

ROZEE.PK

<div><div><div><div><b>1.</b> <b>Purpose
</b></div><div>The objective of this consultancy is to develop a mechanism to revise antimicrobials listed in National Essential Medicines List (NEML) of Pakistan and a Pakistan-specific Access, Watch, Reserve (AWaRe) list of antibiotics in NEML based on the antimicrobial resistance (AMR) and antimicrobial use (AMU) trend. The list will be developed and finalized with the involvement of key stakeholders and accompanied by a practical implementation framework for integration into national antimicrobial governance mechanisms, including prescribing, procurement, stewardship, and regulatory controls..</div><br>
<div></div>
<div><b>
2.</b> <b>Background</b></div>
<div>
AMR is recognized globally and within Pakistan as a critical public health challenge. The WHO&rsquo;s AWaRe classification categorizes antibiotics based on resistance potential, utilization, and spectrum of activity, aiming to guide appropriate antibiotic use. The AWaRe list in low-and-middle income countries (LMICs) guides evidence-based AMR policies in monitoring antibiotic use, regulating over the counter sales and improve prescription-based access to essential antibiotics.
</div><div>The National Institute of Health (NIH) is the National AMR focal point and collects and reports AMR data from sentinel sites, reporting to national and global platforms for evidence-based policies. The Drug Regulatory Authority of Pakistan (DRAP) is AMU focal point to regulate and monitor AMU under national drug regulatory legislation in coordinating with provincial stakeholders.
</div><div>In 2023, DRAP had a consultation with engagement of national experts in the field, and a consultant was engaged to formulate a comprehensive desk review and collect AMR data with the support of NIH from federal and provincial levels, with representation from both the public and private sectors.</div>
<div>
WHO Pakistan is providing technical support to NIH and DRAP for AWaRe classification of antibiotics included in NEML and in the systematic development of Pakistan&rsquo;s first AWaRe list of essential antibiotics with active engagement of stakeholders. The AWaRe list will be used a tool for monitoring antibiotic consumption, defining targets and monitoring the effects of stewardship policies that aim to optimize antibiotic use and curb AMR.</div><br>
<div></div>
<div><b>
3.</b> <b>Work to be performed.</b></div>
<div>
WHO, DRAP and NIH will develop a core group of key stakeholders to oversee the national adaptation and implementation of the WHO AWaRe classification in Pakistan. The consultant will develop an inception report plan and lead the adaptation process, which will involve a contextual review using WHO&rsquo;s methodology, followed by a comprehensive action plan with timeline to integrate the adapted list into Pakistan&rsquo;s health system, through regulatory, prescribing, procurement, and monitoring measures.</div><br>
<div>
</div><div>The consultant is expected to coordinate with WHO, NIH and DRAP focal points team regularly for the refinement and collection of the required information. The methodology will be in alignment with DRAP, NIH guidance for the tasks and approaches mentioned below and consultant will take the lead in reporting against the deliverable.WHO will facilitate a two-day consultation of Technical Working Group (TWG) of relevant experts (federal/provincial) to support national contextualization of the AWaRe classification and guide its integration into the health system through a tailored implementation plan.</div><br>
<div></div>
<div><b>
Output 1: </b><b>Desk review and </b><b>inception report for WHO AWaRe adaptation and implementation planning with timelines.
</b></div><div>l Deliverable 1.1: Conduct a desk review of current global and national guidelines on AWaRe classification. Prepare an inception report detailing the methodology of national adaptation and implementation, with stakeholder mapping and establishing timelines.</div>
<div>
l Deliverable 1.2: Develop a draft AWaRe list adapted to Pakistan&rsquo;s context using the WHO-recommended methodology and available AMR/AMU data, along with comprehensive technical recommendations and guidance for its integration into the health system.</div>
<div>
l Deliverable 1.3: Disseminate the draft list and implementation plan with stakeholders, including DRAP, NIH, and WHO and incorporate their feedback.</div><br>
<div><b>
</b></div><div><b>Output 2: Finalize </b><b>AWaRe list</b><b> through national consultation and </b><b>prepare a comprehensive report</b> <b>with </b><b>clear recommendations and guidelines.</b></div>
<div>
l <b>Deliverable 2.1:</b><b> </b>Conduct an online survey among healthcare professionals across all provinces to get feedback and build consensus on the list.</div>
<div>
l <b>Deliverable 2.2</b><b>:</b> Develop the concept note, agenda and facilitate a two-day Technical Working Group (TWG) consultation with federal and provincial experts, to review the results from survey and review and validate the adapted AWaRe list and incorporate inputs for implementation.
</div><div>l <b>Deliverable 2.3: </b>Finalize the adapted AWaRe list and finalize the comprehensive implementation plan to integrate into Pakistan&rsquo;s health system, covering regulatory alignment, prescribing practices, procurement processes, and monitoring mechanisms based on the TWG consultation.</div>
<div>
l <b>Deliverable 2.3:</b> Submit a report summarising consultative feedback and recommendations.</div><br>
<div>
</div><div><b>4.</b> <b>Technical Supervision</b></div>
<div>
The selected Consultant will work on the supervision of:</div>
<div>
Responsible Officer: Team Lead, HSD</div>
<div>
Manager: Head of WHO Office</div><br>
<div></div>
<div><b>
5.</b> <b>Duration: 30 working days spread over two month.</b></div><br>
<div><b>
</b></div><div><b>6.</b> <b>Specific requirements</b></div>
<div>
Essential qualifications:</div>
<div>
Advanced university degree (Master&rsquo;s level or above) in public health, health systems, microbiology, infectious diseases, medicines, and/or pharmacy sciences.</div><br>
<div></div>
<div>
Experience required (essential): 7 to 10 years of progressive experience in public health, infectious diseases, clinical microbiology, or clinical pharmacy, with demonstrated involvement in antimicrobial stewardship initiatives.</div>
<div>
Experience working with the WHO AWaRe classification system, including its application in hospital or community settings to optimize antibiotic use.</div><br>
<div></div>
<div>
Experience (desirable): Preferably working on patient safety, preferably with work in low- and middle-income countries.</div><br>
<div>
</div><div>Technical skills and knowledge:</div>
<ul>
<li>Demonstrated skills in complex document review, organizational development, and stakeholder engagement including multidisciplinary teams.</li>
<li>Superior editing and analytical skills.</li></ul><br>
<div></div>
<div>
Language requirements:</div>
<div>
Excellent command of both English and the local language.</div><br>
<div></div>
<div><b>
7.</b> <b>Place of assignment:</b> Remote<br>
</div><br>
<br>
</div><div></div><div><h4 class="jobSectionHeader"><b>TOTAL POSITIONS</b></h4>
<p>1</p>
<h4 class="jobSectionHeader"><b>POSTED ON</b></h4>
<p>October 22, 2025</p>
<h4 class="jobSectionHeader"><b>EXPIRY DATE</b></h4>
<p>October 29, 2025</p>
<h4 class="jobSectionHeader"><b>BUSINESS</b></h4>
<p>WHO</p>
<h4 class="jobSectionHeader"><b>CATEGORY</b></h4>
<p>Health &amp; Medicine</p>
<h4 class="jobSectionHeader"><b>JOB TYPE</b></h4>
<p>Consultant</p>
<h4 class="jobSectionHeader"><b>MINIMUM EDUCATION</b></h4>
<p>Masters
</p><h4 class="jobSectionHeader"><b>CAREER LEVEL</b></h4>
<p>Consultant
</p><h4 class="jobSectionHeader"><b>MINIMUM EXPERIENCE</b></h4>
<p>7 Years(Please refer to Job Description section for details)</p></div></div></div>

CONSULTANT (AWARE)

Julphar

Overview <p>At Julphar, we are on a journey of culture transformation & our mission is to provide a better quality of life for the entire family by delivering best in class solutions and real value with compassion and professionalism. Our core values: Respect, Collaboration, innovation, Integrity and Compassion - Combined with a focus on diversity, inclusion, and equal opportunities - are key drivers in our aim to make a positive impact on the lives of the patients we serve, enable Talents, create a healthy work environment, and accomplish our goals through world-class research and with the compassion and commitment of our employees.</p> Microbiological Testing & Analysis <ul> <li>Perform testing of sterile samples including Sterility, LBPC (Limulus-Based Pyrogen Test), and BET (Bacterial Endotoxin Test) with proper documentation.</li> <li>Conduct testing of non-sterile samples, such as Microbial Limit Test (MLT) and Bioburden, along with accurate record-keeping.</li> <li>Perform microbiology assay testing and document results in compliance with GMP.</li> <li>Carry out microbiology culture testing including maintenance, sub-culturing, Growth Promotion Testing (GPT), and microbial identification.</li> </ul> Water & Environmental Testing <ul> <li>Perform water testing, release analysis, and related documentation.</li> <li>Conduct environmental monitoring in classified areas across Julphar production plants and microbiology labs, ensuring accurate and timely documentation.</li> </ul> Lab Support Activities <ul> <li>Execute various microbiology lab support activities including equipment monitoring, cleaning validations, and media preparation.</li> <li>Monitor equipment and area temperatures using Vaisala/SIRIUS systems.</li> <li>Ensure real-time documentation and compliance for all assigned tasks.</li> <li>Handle sample and result entries, reservation creation, and notification processes in SAP.</li> </ul> Compliance & Documentation <ul> <li>Adhere strictly to Good Laboratory Practices (GLP), Data Integrity, and Good Documentation Practices (GDP).</li> <li>Prepare and review Standard Operating Procedures (SOPs) and support microbiology-related qualification/validation documentation.</li> <li>Participate in internal and external audits and promptly report any deviations, OOS (Out of Specification), OOL (Out of Limit), or excursions.</li> <li>Manage documentation and deviation handling through eQMS (Amplelogic system).</li> </ul> Safety & Best Practices <ul> <li>Follow all safety protocols and ensure a clean and compliant laboratory environment.</li> <li>Ensure full compliance with company policies, GMP, and regulatory guidelines.</li> </ul> Core Competencies <ul> <li>Strong sense of accountability and ownership</li> <li>Highly disciplined, motivated, and well-organized</li> <li>Excellent process compliance and implementation skills</li> <li>Effective time and task management</li> <li>Proficient English communication skills (verbal and written)</li> </ul> Qualifications & Functional Knowledge <ul> <li>Bachelor's or Master's Degree in Microbiology or other Biological Sciences</li> <li>4-6 years of relevant experience in a pharmaceutical microbiology lab (preferably in sterile and non-sterile product testing)</li> <li>Proficient in computer applications including MS Word, Excel, and PowerPoint</li> <li>Familiarity with SAP, eQMS (Amplelogic), and temperature monitoring systems like Vaisala/SIRIUS is a plus</li> </ul> <p>We value people from different backgrounds. Could this be your story? Apply today or visit to read more about us and the journey of Julphar</p><img src="https://www.jobg8.com/Tracking.aspx?%2fU1YYyTTTkYM4d6W9QU4jZKMOTHexHmGr" width="0" height="0" />

Specialist - Quality Control

EVA Pharma

<p></p><div><p>Join EVA Pharma, a leading pharmaceutical company dedicated to empowering the fight for health and well-being as a fundamental human right. Recognized and certified as a best place to work, we are committed to fostering a supportive and innovative environment for our team members.</p><p></p><p><b>
Job Summary:
</b></p><p>We are seeking a passionate and talented &ldquo;Microbiology Section Head&rdquo; to join our dynamic team in <b>Sudair - Saudi Arabia.</b> The ideal candidate will contribute to our mission of enhancing human health and well-being, ensuring that we meet the highest standards of excellence in our industry.</p><p></p><p><b>
Key Responsibilities:</b></p><ul>
<li>
Lead, manage, and mentor the microbiology team responsible for both sterile and non-sterile products.</li>
<li>Foster a collaborative and high-performance culture within the team, ensuring adherence to GMP, regulatory requirements, and internal quality standards.</li>
<li>Oversee all microbiological testing activities, including sterility testing, microbial limit testing, bioburden analysis, endotoxin testing, and environmental monitoring.</li>
<li>Prepare for and support internal and external audits, ensuring laboratory operations are always audit-ready.</li>
<li>Ensure that validated methods are transferred effectively to the production environment and maintained in compliance with regulatory requirements.</li>
</ul><p><b>
Requirements</b></p><ul><li>
Bachelor&rsquo;s degree in pharmacy or microbiology. Master of Business Administration is a plus.
</li></ul><ul><li>6-9 years of experience in a related field.
</li><li>GMP, GLP, ICH, and pharmacopeial compliance.</li>
<li>OOS/OOT investigation handling.</li></ul></div>

Microbiology Section Head

5th Avenue Recruiting

<div><p>We are looking for an experienced Microbiologist to join our Quality Control team in a nutraceutical manufacturing company. The ideal candidate will be bilingual (English &amp; Spanish) and have a strong background in laboratory testing, microbiological analysis, and quality control procedures. This role is critical to ensuring our products meet the highest safety and compliance standards.</p><br>
<p></p>
<p><b>
Key Responsibilities:</b></p>
<ul>
<li>Conduct microbiological testing and analysis of raw materials, in-process samples, and finished products</li>
<li>Perform environmental monitoring to ensure a contamination-free production environment</li>
<li>Maintain and calibrate laboratory equipment to ensure accurate testing results</li>
<li>Document and report test results in compliance with GMP and regulatory guidelines</li>
<li>Assist in investigating microbial contamination issues and implement corrective actions</li>
<li>Work closely with the Quality Assurance and Production teams to ensure compliance with industry standards</li>
<li>Follow laboratory safety protocols and maintain cleanliness of the microbiology lab</li>
<li>Support regulatory inspections and audits by providing accurate records and reports</li></ul><br>
<p></p>
<p><b>
Qualifications:</b></p>
<ul>
<li>Bachelor&rsquo;s degree in Microbiology, Biology, or a related field</li>
<li>Previous experience in a microbiology laboratory within the nutraceutical, pharmaceutical, or food industry</li>
<li>Strong understanding of GMP, FDA, and regulatory requirements</li>
<li>Ability to perform microbiological testing and interpret results accurately</li>
<li>Bilingual (English &amp; Spanish) is required</li>
<li>Proficiency in Microsoft Office and laboratory software</li>
<li>Detail-oriented with strong analytical and problem-solving skills</li></ul></div><p></p>

Microbiology

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