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Biomedical Engineer (Clinical, Genomics, Stem cell, GMP Peptide Production)

Holden Grant
Abu Dhabi, UAE
Full Time
Senior
Onsite
1 months ago
Clinical PathologyGenomicsGMP Peptide ProductionMass Spectrometry (LC MS)HPLCLiquid Handling Systems
Free

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Clinical PathologyGenomicsGMP Peptide Production
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Job Summary

  • We are seeking a highly skilled Biomedical Engineer with expertise in clinical pathology, genomics, and GMP peptide production.
  • The ideal candidate will bridge advanced instrumentation, stem cell processes, sequencing platforms, and mass spectrometry to support innovative clinical, genomic, and peptide workflows.

Key Responsibilities

  • Design, develop, and maintain biomedical instrumentation in a clinical pathology environment (e.g., Roche Cobas Pure and other clinical analyzers).
  • Integrate and optimize genomic workflows, including whole genome sequencing (WGS) using MGI, PacBio, & Element Bioscience platforms.
  • Operate and maintain liquid handling systems (e.g., Hamilton, Beckman Coulter, Eppendorf, Tecan) to automate clinical, genomic, and peptide assays.
  • Lead and support stem cell processes, including cell culturing, differentiation, and organoid development, ensuring precision and reproducibility.
  • Conduct GMP peptide synthesis workflows, using mass spectrometry (LC MS), HPLC, and other analytical techniques.
  • Perform in house calibration of instruments to ensure accuracy and compliance with GMP standards.
  • Collaborate closely with automation and robotics engineers to integrate autonomous systems into the facility, ensuring a fully automated, autonomous workflow.
  • Collaborate in biobanking processes, ensuring sample integrity, tracking, and storage.
  • Support stem cell platform operations and experimental design, ensuring precise protocols.
  • Conduct mass spectrometry analysis (LC MS) for peptide validation and biomarker discovery.
  • Troubleshoot technical issues with instruments and provide timely solutions to maintain workflow efficiency.
  • Maintain strong communication and collaborate cross functionally with clinical teams, researchers, IT, and automation/robotics teams, fostering a culture of innovation and teamwork.

Qualifications

  • Bachelor’s or Master’s degree in Biomedical Engineering, Clinical Engineering, or related field; PhD is a plus.
  • Minimum of 3 5 years of hands on experience in clinical pathology, working with instruments like Cobas Pure.
  • Strong experience with genomic sequencing platforms and liquid handling automation (e.g., Hamilton, Beckman Coulter, Tecan, Eppendorf).
  • Experience in GMP peptide synthesis, mass spectrometry (LC MS), and HPLC for peptide validation and biomarker analysis.
  • Familiarity with stem cell platforms, including cell culturing and organoid development.
  • Ability to perform in house calibration of instruments to ensure precise performance and GMP compliance.
  • Ability to work closely with automation and robotics engineers to integrate autonomous systems and drive facility wide automation.
  • Proficiency in troubleshooting advanced biomedical equipment and ensuring GMP compliance.
  • Strong analytical skills, with attention to detail, and ability to work in a regulated GMP environment.

Additional Information

  • Education: Bachelor's (Required)
  • Experience: Clinical Pathology: 3 years (Required)
  • Experience: genomic sequencing platforms and liquid handling automation: 3 years (Preferred)
  • Experience: GMP peptide synthesis, mass spectrometry: 3 years (Preferred)
  • Work Location: In person

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