Biomedical Engineer (Clinical, Genomics, Stem cell, GMP Peptide Production)
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Key skills for this role
About the Role
We are seeking a highly skilled Biomedical Engineer with expertise in clinical pathology, genomics, and GMP peptide production. The role involves designing and maintaining biomedical instrumentation, integrating genomic workflows, operating liquid handling systems, and leading stem cell processes.
Key Skills for This Role
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
- 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
- Collaborate in biobanking processes, ensuring sample integrity, tracking, and storage
- Support stem cell platform operations and experimental design
- Conduct mass spectrometry analysis (LC MS) for peptide validation and biomarker discovery
- Troubleshoot technical issues with instruments and provide timely solutions
- Maintain up to date knowledge of emerging technologies in clinical diagnostics, genomics, stem cell research, mass spectrometry, and GMP practices
Requirements
- 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
- Proficiency in troubleshooting advanced biomedical equipment and ensuring GMP compliance
Full Job Posting
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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