Manufacturing Operator/Technician (Immunology, BioTech)
Quick Summary
MAT Research is a pioneering company in the field of pyrogen testing, committed to ushering in a new era of ethical and accurate diagnostics. Since 2016, we have been leading the development of the Monocyte Activation Test (MAT), an animal-free alternative to traditional Rabbit Pyrogen Tests.
MAT Research is a pioneering company in the field of pyrogen testing, committed to ushering in a new era of ethical and accurate diagnostics. Since 2016, we have been leading the development of the Monocyte Activation Test (MAT), an animal-free alternative to traditional Rabbit Pyrogen Tests. Our ready-to-use MAT kits offer a robust and highly reliable method for detecting a broad range of pyrogens in parenteral drugs. ISO:9001:2015 certified, we uphold the highest standards of quality in all our products and services. By focusing on in-vitro human-based testing, we aim to drastically increase patient safety while saving hundreds of thousands of animal lives each year. We are steadfast supporters of the European Pharmacopoeia's vision to replace animal-based tests with MAT by 2026. For more details, go to our job page.
Responsibilities
~1 min read- →
Manufacturing & Production
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Equipment & Process Maintenance
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Quality Control & Compliance
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Material & Inventory Management
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Process Improvement & Reporting
Responsibilities
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Execute end-to-end manufacturing processes, including preparation, formulation, and packaging of MAT kits.
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Follow Standard Operating Procedures (SOPs), batch records, and Good Manufacturing Practices (GMP) to ensure consistency and quality.
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Assist in the scale-up of manufacturing processes, optimising workflow efficiency.
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Operate and maintain bioprocessing and immunoassay equipment.
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Perform routine calibration, sterilisation, and maintenance of manufacturing tools.
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Monitor and troubleshoot production deviations or process inefficiencies.
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Conduct in-process quality control tests to ensure product reliability.
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Work closely with Quality Assurance (QA) teams to maintain compliance with ISO:9001:2015, GMP, and regulatory requirements.
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Maintain accurate batch records and production documentation to ensure traceability.
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Prepare, measure, and handle biological materials, PBMCs, reagents, and consumables.
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Ensure proper storage conditions and inventory tracking for raw materials and finished products.
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Support continuous improvement initiatives to optimise production workflows.
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Assist in developing new SOPs, technical documentation, and training materials.
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Report deviations and contribute to troubleshooting investigations and corrective actions.
Location & Eligibility
Listing Details
- First seen
- May 6, 2026
- Last seen
- May 8, 2026
Posting Health
- Days active
- 0
- Repost count
- 0
- Trust Level
- 51%
- Scored at
- May 6, 2026
Signal breakdown
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