ADNIP (Abu Dhabi National Industrial Projects) is actively hiring a QC Microbiologist to join its quality control team in Abu Dhabi, UAE. This full-time laboratory role is responsible for carrying out microbiological testing, quality control analysis, environmental monitoring, and GMP compliance activities — ensuring the microbiological integrity and quality assurance standards of the company’s industrial manufacturing operations. Interested candidates or referrals should send their CV to hr@adnip.ae.
About ADNIP — Abu Dhabi National Industrial Projects
Organisation: ADNIP — Abu Dhabi National Industrial Projects — an Abu Dhabi based industrial manufacturing and production organisation
Sector: Industrial manufacturing — operating within Abu Dhabi’s strategically important industrial and production sector
Location: Abu Dhabi, UAE — the capital of the UAE and the centre of the country’s industrial, energy, and manufacturing activity
Quality Focus: A quality-driven organisation where the QC Microbiology function plays a central role in ensuring manufacturing compliance, product integrity, and regulatory adherence
Contact: Send your CV or referrals to: hr@adnip.ae
QC Microbiologist Scope — Abu Dhabi
Microbiology Testing: Conducting routine and non-routine microbiological analyses on raw materials, in-process samples, and finished products
Environmental Monitoring: Air, surface, and water sampling programmes across manufacturing and cleanroom environments
GMP Compliance: Ensuring all laboratory activities comply with Good Manufacturing Practice standards and applicable UAE regulatory requirements
Documentation: Accurate, real-time recording of all microbiological test results, deviations, and QC reports
CAPA Support: Investigating out-of-specification microbiological results and supporting corrective and preventive action implementation
Position Overview
This QC Microbiologist role at ADNIP in Abu Dhabi is a technically demanding and quality-critical position within the organisation’s Quality Control laboratory. As QC Microbiologist, you will be responsible for performing a comprehensive range of microbiological testing and quality control activities — including the testing of raw materials, in-process samples, and finished products for microbiological quality and safety; conducting environmental monitoring programmes across manufacturing and controlled environments; maintaining accurate and audit-ready microbiological records; ensuring GMP and regulatory compliance across all laboratory activities; investigating out-of-specification (OOS) results; supporting CAPA processes; and contributing to the continuous improvement of microbiological QC methods and procedures. This role is suited to a technically proficient microbiologist with hands-on laboratory experience, strong attention to detail, and a genuine commitment to quality excellence in a UAE industrial manufacturing setting.
Why This Role Matters: As QC Microbiologist at ADNIP in Abu Dhabi — in a quality control laboratory role that directly protects the microbiological integrity of industrial manufacturing operations — you will apply your microbiology expertise to ensure that every product that leaves the facility meets the highest microbiological quality and safety standards, maintain the environmental monitoring and testing programmes that protect manufacturing environments and product quality from microbial contamination risks, contribute your analytical skills and laboratory precision to an organisation that genuinely values quality as the foundation of its operational credibility and customer trust, and build a specialised microbiology laboratory career within Abu Dhabi’s dynamic and growing industrial manufacturing sector — one of the UAE’s most strategically important economic pillars under Vision 2030 and the Abu Dhabi Economic Vision 2030 industrial development programme.
Key Responsibilities
Microbiological Testing — Raw Materials, In-Process & Finished Products
- Perform routine and non-routine microbiological testing on incoming raw materials, in-process production samples, and finished goods — executing tests for total viable count (TVC), yeast and mould count, specific pathogen detection, sterility testing, and any other microbiological quality parameters applicable to the company’s product and regulatory requirements
- Operate and maintain microbiological testing equipment and analytical instruments — including incubators, autoclaves, laminar flow cabinets, colony counters, microscopes, and any automated microbiology systems in use within the QC laboratory — following validated operating procedures and equipment maintenance schedules
- Prepare microbiological growth media and reagents according to validated recipes and compendial standards — ensuring that all prepared media pass appropriate growth promotion, sterility, and pH quality control tests before use in testing activities
- Interpret and evaluate microbiological test results against defined acceptance criteria — accurately recording all results in real time, flagging out-of-specification results immediately according to OOS investigation procedures, and ensuring that test interpretation follows validated methods and applicable pharmacopoeial or regulatory standards
Environmental Monitoring Programme
- Execute the environmental monitoring programme across manufacturing, controlled, and cleanroom environments — conducting scheduled air sampling (active and passive), surface contact sampling, water sampling, and personnel monitoring in accordance with the approved environmental monitoring schedule and sampling plan
- Record all environmental monitoring results in real time — maintaining accurate, complete environmental monitoring data records that provide full traceability of each sampling event, result, and any associated action taken in response to alert or action limit exceedances
- Investigate environmental monitoring exceedances — conducting root cause analysis of alert and action limit breaches, coordinating with production, engineering, and HSE teams to identify contributing factors, and supporting the implementation of corrective actions that prevent recurrence
- Trend environmental monitoring data systematically — tracking and reporting on environmental monitoring performance over time to identify emerging contamination risks, seasonal patterns, or facility condition trends that may require proactive intervention before alert or action limits are exceeded
GMP Compliance, Documentation & Regulatory Standards
- Ensure all microbiological laboratory activities are conducted in full compliance with applicable Good Manufacturing Practice (GMP) standards, UAE regulatory requirements, and the organisation’s validated laboratory methods and standard operating procedures
- Maintain accurate, complete, and audit-ready microbiological QC records — including test worksheets, environmental monitoring logs, media preparation records, equipment calibration and maintenance logs, analyst training records, and all other documentation required to demonstrate GMP compliance and analytical data integrity
- Follow the organisation’s document control system for all laboratory SOPs, test methods, and quality records — ensuring that only current approved versions of procedures are in use, that superseded documents are correctly archived, and that all documentation is completed with the accuracy and professional care that GMP compliance requires
- Maintain strict aseptic technique, biosafety standards, and laboratory hygiene practices throughout all microbiological testing activities — ensuring the safety of laboratory personnel, the integrity of test samples, and the compliance of the laboratory environment with applicable biosafety and GMP requirements
OOS Investigations, CAPA & Continuous Improvement
- Conduct structured Out-of-Specification (OOS) investigations for any microbiological test results that fall outside defined acceptance criteria — following the approved OOS investigation procedure, conducting Phase I laboratory investigation and Phase II process investigation activities, and documenting all findings and conclusions accurately and completely
- Support the development and implementation of Corrective and Preventive Actions (CAPA) for microbiological quality deviations — contributing laboratory expertise and test data analysis to the root cause identification process, and verifying through follow-up testing or monitoring that implemented corrective actions have effectively resolved the identified microbiological quality issue
- Contribute to the validation and verification of new microbiological test methods — supporting method validation studies, preparing validation documentation, and ensuring that new or updated test methods meet regulatory and GMP validation requirements before implementation in routine QC testing
- Participate actively in internal quality audits, regulatory inspections, and customer audits as they relate to the QC microbiology laboratory — providing accurate responses to auditor queries, demonstrating laboratory practices, and contributing to the preparation of audit readiness activities
Quality Data Reporting & Cross-Functional Collaboration
- Prepare microbiological quality control reports and performance summaries for the QC Manager and relevant stakeholders — providing timely, accurate, and clearly presented microbiological data that supports product release decisions, quality management reviews, and regulatory compliance reporting
- Collaborate effectively with Production, Quality Assurance, Regulatory Affairs, and Engineering teams — ensuring that microbiological quality data, environmental monitoring findings, and OOS investigation outcomes are communicated accurately and promptly to all relevant cross-functional partners
- Support the onboarding and basic microbiology training of new laboratory analysts or technicians — providing practical guidance on correct aseptic technique, laboratory safety procedures, test method execution, and documentation standards
Qualifications & Requirements
Education
- Bachelor’s degree or higher in Microbiology, Applied Microbiology, Pharmaceutical Microbiology, Biological Sciences, or a closely related field from a recognised accredited university — a relevant science degree is required for this QC Microbiologist role
- Postgraduate qualification (MSc) in Microbiology, Quality Assurance, or a related field is an advantage — demonstrating advanced academic preparation for the technical and quality management responsibilities of this position
Experience Requirements
- Practical hands-on microbiological laboratory experience — preferably in a GMP-regulated quality control environment within the pharmaceutical, food, industrial, or healthcare sectors — with demonstrated proficiency in microbiological testing techniques and GMP documentation practices
- Experience with environmental monitoring programmes — including air, surface, water, and personnel sampling — and knowledge of alert and action limit management, trend analysis, and contamination investigation procedures in a controlled manufacturing environment
- Familiarity with pharmacopoeial microbiological test methods (USP, BP, EP, or equivalent) or applicable food or industrial microbiological testing standards — and experience applying validated test methods in a GMP quality control laboratory context
- Strong attention to detail, accuracy, and documentation discipline — the core professional qualities that are non-negotiable in a GMP microbiological laboratory where data integrity, analytical precision, and complete record-keeping are fundamental requirements
How to Apply — ADNIP QC Microbiologist
Send your CV directly to: hr@adnip.ae
Position: QC Microbiologist — Abu Dhabi, UAE
Know a great candidate? Tag them or forward this opportunity — referrals are welcome
About QC Microbiologist Careers in Abu Dhabi’s Industrial Sector
Abu Dhabi is one of the UAE’s most important centres for industrial manufacturing, pharmaceutical production, food processing, and petrochemical operations — with a growing portfolio of manufacturing facilities that require sophisticated quality control and laboratory expertise to maintain the regulatory compliance, product integrity, and operational credibility that global markets demand. For microbiologists with GMP laboratory backgrounds, Abu Dhabi’s industrial sector offers outstanding career opportunities — combining competitive compensation in a tax-free environment, professional exposure to internationally certified manufacturing quality systems, and the professional satisfaction of contributing directly to the microbiological quality and safety of products that reach consumers across the UAE and wider region.
ADNIP — Abu Dhabi National Industrial Projects — is part of Abu Dhabi’s strategically important industrial manufacturing landscape, and a QC Microbiologist role here represents a meaningful professional opportunity to apply technical microbiology expertise in a quality-focused, compliance-driven industrial environment where accurate testing, rigorous documentation, and a genuine commitment to GMP standards are rightly valued as foundational contributors to manufacturing excellence.
Career Excellence: Join ADNIP as QC Microbiologist in Abu Dhabi, UAE — where your microbiology expertise, GMP laboratory skills, environmental monitoring knowledge, and commitment to analytical precision will protect the microbiological quality and integrity of manufacturing operations and advance your quality control career in one of the UAE’s most strategically important and professionally rewarding industrial manufacturing environments.
Who Should Apply?
- QC Microbiologists with GMP Experience: Holding a microbiology or biological sciences degree and hands-on GMP quality control laboratory experience in pharmaceutical, food, or industrial manufacturing — ready for a QC Microbiologist role at ADNIP in Abu Dhabi
- Environmental Monitoring Specialists: With direct experience executing and managing environmental monitoring programmes in controlled manufacturing environments — familiar with alert and action limit management, contamination investigation, and monitoring data trending
- Pharmaceutical or Food Microbiology Lab Scientists: With USP, BP, EP, or applicable food standard microbiological testing experience — comfortable with total viable count, pathogen detection, sterility testing, and pharmacopoeial method execution in a regulated GMP laboratory
- OOS Investigation & CAPA Experienced Microbiologists: With practical experience conducting Out-of-Specification investigations, performing root cause analysis of microbiological quality deviations, and supporting CAPA implementation and verification in a GMP quality control environment
- UAE-Based Microbiology Laboratory Professionals: Currently based in Abu Dhabi or the UAE — with the right academic qualification, GMP laboratory experience, and commitment to microbiological quality excellence to join ADNIP’s quality control team and contribute to its manufacturing quality mission
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