Quality Control Microbiologist (Bioassay)

About the Client:

Our client is a leading global biopharmaceutical company focused on developing transformative treatments for serious diseases. Their mission is to improve patient lives through innovation in areas like HIV/AIDS, liver disease, and oncology.

The Role:

As a QC Microbiologist specialising in Bioassay, you will conduct a range of analytical techniques, ensuring compliance with industry standards and providing technical expertise for key projects. You will work closely with cross-functional teams to drive quality and continuous improvement.

Key Responsibilities:

• Perform Bioassay techniques (e.g., ELISA, Flow Cytometry, Cell-based assays)
• Support method transfers and validations; review data to ensure specification compliance
• Lead investigations, troubleshoot issues, and contribute to technical projects
• Develop and refine protocols and procedures in line with regulatory standards
• Engage with cross-functional teams and deliver technical presentations as required

Your Skills & Experience:

• Strong experience in Bioassay techniques, including ELISA, Receptor Binding, and Cell-based assays
• Knowledge of GMPs, GLPs, and regulatory requirements for Biologics testing
• Familiarity with software such as Softmax Pro, LIMS, and Trackwise
• Proven communication skills, with the ability to work collaboratively and independently

Education & Experience:

• BSc with 4+ years of relevant experience, or MSc with 2+ years in Biology, Biotechnology, or a related discipline
• Prior experience in a Biologics testing lab is preferred
• If you’re a detail-oriented professional with a passion for excellence, apply now to join this dynamic team where your expertise will make a difference!

This is a fantastic opportunity to grow your career, contribute to life-changing work, and be part of a collaborative, purpose-driven team. If you’re ready to make an impact, apply today to join our client’s team!

How to Apply:

To apply, please submit your CV outlining your qualifications and experience relevant to this role.

Please note: You must be able to work in Ireland or the EU without restriction or sponsorship to be eligible for this role. If you are interested in finding out more about this role or others, please contact Jada Kirlew at jkirlew@i-pharmconsulting.com or call: 

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