BIOMEDICAL ENGINEER JOB DESCRIPTION

Pre-clinical validation data that cannot support an FDA or Health Canada regulatory submission delays a product by months and puts patient access at risk. The Biomedical Engineer is the person who prevents that outcome, owning the experimental design, device characterization, and technical documentation that move a medical device from concept through submission-ready evidence packages. This role sits within R&D or process development teams, working alongside cell biologists, biomaterial scientists, and data scientists. ISO 14971 risk management and Design History File compliance define the boundaries of the work.

As the Biomedical Engineer, you will design, validate, and characterize medical devices and cell-based therapeutics, generating the experimental evidence and regulatory documentation that bring novel products to clinical use. You will operate within a cross-functional R&D or process development team, contributing to milestone-driven programs that span pre-clinical testing through regulatory submission.

Career Impact: Deep experience owning pre-clinical study design and FDA or Health Canada regulatory submissions positions a Biomedical Engineer as a domain authority in the medical device development field within 2 to 3 years.

Business Impact: The experimental results and design documentation this role produces are the direct basis on which regulators evaluate device safety, meaning a single submission package can determine whether a therapy reaches patients.

Growth Opportunity: Mastery of in-vivo characterization, DOE methodology, and regulatory compliance documentation opens advancement toward Senior Biomedical Engineer, Principal Scientist, or R&D Program Lead roles.

• Design and execute in vitro and in vivo assays to characterize device function against pre-defined performance specifications.
• Develop device prototypes and design concepts spanning tissue engineering constructs, microfluidic structures, and biosensor assemblies for pre-clinical evaluation.
• Conduct design of experiments using DOE methodology to model critical-to-quality performance variables and establish optimal process input set points.
• Apply statistical analysis methods to acquired experimental and clinical data to generate performance insights and transfer functions.
• Maintain regulatory documentation including Design History Files, SOPs, test protocols, and study reports in compliance with FDA and Good Clinical Practice requirements.
• Partner with manufacturing, regulatory, and cross-functional engineering teams to develop stage-appropriate device manufacturing and process transfer plans.
• Support intellectual property protection by contributing to patent documentation and presenting experimental results to internal and external stakeholders.
• Lead risk analysis activities using ISO 14971 methodology across device design and process development programs.

• Bachelor's degree in biomedical engineering, mechanical engineering, or a related engineering discipline, or equivalent work experience.
• 2 or more years of hands-on experience in medical device or biotech R&D, with direct involvement in pre-clinical device development or characterization.
• Demonstrated ability to design, execute, and interpret experiments using structured DOE methodology and applied statistical analysis.
• Working knowledge of FDA regulatory frameworks and Good Clinical Practice requirements applicable to medical device development.
• Experience developing and maintaining technical documentation including SOPs, test protocols, engineering reports, and laboratory notebooks.
• Proven ability to manage multiple concurrent technical projects independently within milestone-driven R&D programs.
• Strong written and verbal communication skills, with experience presenting experimental results to multidisciplinary stakeholders.

• Advanced degree (Master's or PhD) in biomedical engineering, electrical engineering, or a closely related field, with academic or industry research experience in implantable devices or biosensor development.
• Familiarity with ISO 14971 risk management processes and Design History File requirements for combination products or Class II and Class III medical devices.
• Experience with signal processing techniques applied to physiological signals such as ECG, PPG, or subcutaneous biosensing data.
• Knowledge of aseptic processing, BSL lab practices, or cell therapy manufacturing processes within a regulated biotech environment.

• Device characterization data package completeness rate, measured against submission-ready documentation standards.
• Pre-clinical study cycle time from protocol approval to final report, tracking experimental throughput per program.
• DOE model accuracy, measured by how well predicted set points match observed in-vivo or in-vitro performance outcomes.
• Number of regulatory documentation items requiring revision after internal or external review, reflecting documentation rigor.
• Patent application contributions per year, measuring intellectual property output from experimental programs.
• Typical tools: Statistical analysis platforms (commonly Minitab or JMP), scientific programming environments (commonly MATLAB or Python), CAD platforms (commonly SolidWorks).

• Base Salary Range: $85,000 to $130,000 annually, depending on seniority and degree level.
• Bonus: 5 to 15 percent annual performance bonus, common in biotech and medical device firms.
• Equity: Stock options or RSUs offered at many venture-backed and mid-size medical device companies.
• Health Benefits: Medical, dental, and vision coverage, typically employer-subsidized at 70 to 90 percent.
• PTO: 15 to 20 days annually, plus standard US federal holidays.
• Common Perks: Professional conference attendance, continuing education support, and lab safety training.

Figures are estimates based on general US market benchmarks and may be outdated. Adjust based on location, company size, and seniority level.

Work authorization in the United States is required for all positions. Employment in this role is contingent on successful completion of a background check, which may include verification of prior employment and education credentials. Reasonable accommodations under the Americans with Disabilities Act are available to qualified applicants and employees upon request. All candidates are evaluated without regard to race, color, religion, sex, national origin, age, disability, veteran status, genetic information, or any other characteristic protected under applicable federal, state, or local law.

The Biomedical Engineer owns the strategic design and fabrication of bioprinted tissue devices, working within a multidisciplinary R&D team of cell biologists, biomaterial scientists, and engineers to advance implantable cell-based therapeutics. Reporting to senior R&D management, this role delivers life-changing tissue therapeutics from discovery through clinical manufacturing, enabling transformative treatments for metabolic and other diseases.

Key Responsibilities

• Design and develop novel bioprinted cell-containing implantable devices that support therapeutic cell function and tissue transplant durability.
• Develop bioprinting technology to generate optimized micro- and macro-architectures of bioprinted tissues that support therapeutic cell function, immune protection, vascularization, and minimized foreign body response.
• Design and test optimal surgical approaches for implantation of cellular devices.
• Perform in vitro and in vivo assays to assess device function.
• Work closely with biologists, biomaterial scientists, and engineers to customize device composition and architectural design for specific indications, including cell therapies for metabolic disease.
• Liaise with manufacturing and regulatory teams to develop stage-appropriate device manufacturing processes.
• Create SOPs, deliver experimental reports, support patent applications, and present experimental results to key internal and external stakeholders.
• Contribute to development of project milestones, timelines, and product deliverables in collaboration with senior R&D management.
• Maintain clear and rigorous experimental records, including electronic laboratory notebooks.
• Become an expert user of Aspect's microfluidic 3D bioprinting technology.

Required Qualifications

• PhD in biomedical engineering or a similar discipline.
• 2+ years in a post-doctoral, biotech, or industry position, with experience developing implantable cell-containing devices preferred.
• Rigorous grounding in fundamental biology and physiology combined with in-depth engineering design and computational foundations.
• Significant academic or industry experience in developing implantable cell-containing tissues or devices for implantation.
• Experience in tissue engineering, 3D bioprinting, and testing devices in pre-clinical or clinical applications is helpful.
• Knowledge of SolidWorks or similar CAD software is advantageous.
• Outstanding attention to detail and experimental and process rigor.
• Intellectually curious with a desire to learn and collaborate effectively in a multi-disciplinary team environment.

Embedded within an international Healthcare project team, the Biomedical Engineer plans and manages laboratory and pharmacy equipment across all project stages from design through commissioning for hospitals and specialized facilities. Working closely with medical staff, hospital engineering departments, suppliers, and internal organizational units, this role ensures accurate specification, cost control, and successful on-site delivery of complex equipment programs.

Core Functions

• Plan laboratory and pharmacy equipment for hospitals and specialized projects, manage room equipment lists, draft catalogues with specifications and quantities, and prepare cost estimates and general specifications.
• Define and describe detailed specifications of laboratory and pharmacy equipment.
• Contact suppliers, request proposals, and process offers.
• Calculate equipment and workload internally.
• Draft time schedules and clarify pre-installation requirements.
• Supervise installation works and organize on-site training for medical equipment.
• Communicate effectively with customers including medical staff and hospital engineering departments.
• Cooperate actively with other organizational units and departments.

Qualifications and Experience

• Technical degree from a technical college, university of applied sciences, or university of technology, or comparable education and equivalent experience in electrical or electronic engineering.
• At least 7 years of working experience in a hospital environment.
• Excellent knowledge of workflows and medical devices in hospitals and research centers.
• Excellent knowledge of state-of-the-art laboratory analysis methods and corresponding manufacturers for laboratory and pharmacy equipment.
• Proven ability to represent and present to diverse audiences.
• Excellent computer skills.
• Excellent language skills in English, with other languages beneficial.
• Excellent team working, communication skills, flexibility, and readiness to travel abroad.

Reporting to engineering leadership, the Biomedical Engineer researches, designs, and develops analog and mixed-signal IC electronics for next-generation smart textile products within a multidisciplinary team of scientists, textile experts, fashion designers, and entrepreneurs. Partnering with mechanical, firmware, data science, software, and industrial design disciplines, this role advances wearable technology from rapid prototype through optimized, cost-effective production-ready designs.

Primary Duties

• Research, design, and develop analog and mixed-signal IC electronics for the next generation of smart textiles including firmware.
• Perform rapid prototyping and validation of electrical designs.
• Optimize designs for power, miniaturization, and cost.
• Bring up PCBs, document bugs, and iterate on designs.
• Develop understanding of RTOS and write application drivers.
• Work closely with teams across mechanical, firmware, data science, software, industrial design, and textile disciplines.
• Aid in the assembly of prototypes and debug issues on the fly.

Skills and Qualifications

• MASc or PhD preferred in electrical or biomedical engineering or related fields.
• 5-10 years of experience with electrical circuit design and firmware development.
• Experience working on embedded systems with embedded communication protocols such as UART, I2C, USB, and SPI.
• Proficient with software such as Altium and Eagle for circuit analysis, debugging, and PCB design.
• Understanding of biosignals and signal processing techniques is an important asset.
• Strong analytical, problem solving, and leadership capabilities.
• Ability to contribute and work effectively in a fast-paced, multidisciplinary environment.

Sitting at the intersection of biomedical engineering and regulatory compliance, the Biomedical Engineer performs and oversees device design, prototyping, and risk analysis as a member of cross-functional product development teams. Operating across human factors research, design controls, and FDA guidance for Combination Products, this role enables the creation and continuous improvement of compliant, market-ready medical devices.

Duties

• Perform or oversee biomedical and mechanical engineering, design, and development work as a BME team member on cross-functional teams.
• Develop design concepts and ideas for new products and product improvements.
• Develop prototypes of design concepts for engineering testing and evaluation.
• Review and approve SOPs, test protocols, and laboratory research reports, and provide laboratory oversight as needed.
• Perform human factors studies, market assessment, or pre-clinical research.
• Lead risk analysis activities and adhere to design controls, documenting all product development work in a Design History File.
• Comply with FDA Regulation and Guidance for Combination Products.

Education and Experience

• Minimum bachelor's degree in biomedical engineering or mechanical engineering.
• Minimum 3-5 years of medical device development experience.
• Knowledge of human factors and usability engineering.
• Conceptual design skills and experience with a variety of manufacturing methods such as injection molding and machining.
• Knowledge of Minitab, SolidWorks, and Microsoft Office.

A key member of a biomedical R&D team, the Biomedical Engineer develops and implements novel signal processing algorithms in MATLAB for patient monitoring and diagnosis based on physiological signals such as ECG, PPG, and EEG. Collaborating across device, data science, and clinical teams as well as funding agencies and regulatory bodies, this role advances algorithm-driven medical device development from clinical data acquisition through FDA and Health Canada regulatory submissions.

Functions

• Develop and implement novel signal processing and analysis algorithms in MATLAB for patient and subject monitoring and aid in diagnosis and therapy based on physiological signals such as ECG, PPG, and EEG.
• Execute and administer R&D programs both independently and collaboratively, and interface with funding agencies and program officials.
• Assist in conceiving new ideas and writing grant proposals.
• Assist with the design and implementation of clinical studies to acquire physiological signals from human subjects for algorithm development and validation.
• Develop and validate algorithms based on acquired human subjects and clinical data, and perform statistical analysis of processed data.
• Develop and maintain regulatory documentation for related clinical studies as per current Good Clinical Practice.
• Prepare scientific reports and publications, and present at scientific conferences.
• Provide support for intellectual property protection and Health Canada and FDA regulatory submissions.
• Work with device and data science teams to implement algorithms in production firmware and server backend.

Experience and Qualifications

• Master's or PhD in biomedical engineering, electrical or computer engineering, or related fields.
• 2+ years of industry experience in signal processing and machine learning.
• Theoretical knowledge and practical experience in biomedical research, particularly in advanced signal processing and analysis.
• Experience with analysis of bio and physiological signals, design of experiments, and modern machine learning techniques.
• Experience in regulated medical software products, cGCP, and medical device industry regulation.
• Proficient in MATLAB and strong programming expertise in Python, C, and SQL.
• Excellent oral, verbal, and written communication skills in English, with experience writing scientific publications and grant proposals.
• Motivated, independent, efficient, and able to handle multiple projects in a small team environment.

Delivering custom cell therapy process equipment depends on the Biomedical Engineer, who designs and tests microfluidic structures, evaluates manufacturing technologies, and maintains rigorous technical documentation within SQZ Biotechnologies' Process Development and Manufacturing group. Based within a cross-functional engineering environment and collaborating closely with external vendors, this role advances the SQZ technology platform toward high-volume production readiness.

Accountabilities

• Evaluate different manufacturing technologies to incorporate into custom process equipment.
• Design and test various microfluidic structures for cell processing.
• Design and implement manufacturing solutions for high volume production.
• Perform hands-on biological laboratory work, data analysis, and maintain technical documentation.
• Develop equipment and component drawings using CAD software.
• Organize and develop plans for independent laboratory experiments and associated laboratory analysis.
• Collaborate across different functional teams to ensure successful completion of necessary studies.
• Establish and maintain communication with vendors and assist with product procurement, testing, and evaluation.

Background and Experience

• Bachelor's or master's degree in biomedical engineering, mechanical engineering, bioengineering, or a related field.
• At least 2 years of experience in the biotechnology or pharmaceutical industry.
• Experience working in a biological lab with understanding of safe lab practices and BSL requirements.
• Experience in cell therapy manufacturing processes and aseptic processing is a plus.
• Proficient in CAD software.
• Strong organizational skills and ability to manage multiple technical projects and priorities simultaneously.
• Excellent oral and written communication skills.

As the Biomedical Engineer, this role designs and develops biomedical equipment and coordinates testing and regulatory compliance for an international development and research firm operating across more than 80 countries. The Process Development team relies on this work to ensure equipment functionality, regulatory adherence, and technical training delivery that directly supports health and development program outcomes worldwide.

Key Deliverables

• Design and develop biomedical equipment.
• Coordinate the testing and analysis processes.
• Test the functionality of equipment and take accuracy, sensitivity, and selectivity measurements.
• Monitor biomedical equipment to ensure compliance with regulatory requirements.
• Provide technical training on equipment operations.

Minimum Qualifications

• Bachelor's degree in biomedical engineering or a related discipline.
• Master's degree in biomedical engineering or a related discipline preferred for senior roles.
• 1-10+ years of experience in biomedical engineering or a related field depending on level.
• Demonstrated knowledge of biomedical regulatory requirements.
• Able to be a real team player with positive vibes.

Biomedical Engineer leads characterization, design of experiments, and data analysis to advance next-generation subcutaneous glucose biosensors within a multidisciplinary medical device team. The work directly supports in-vivo sensor performance optimization, regulatory documentation, and design process transfer that enable safe, reliable biosensing products to reach patients.

Areas of Ownership

• Contribute as a member of multidisciplinary teams to support the development of next generation subcutaneous biosensors with emphasis on glucose sensing.
• Analyze sensing modalities, processes, and system integration.
• Apply best-known methods for robust characterization of various sensor designs using DRM or similar methodology to establish design and process requirements.
• Conduct design of experiments to model statistically significant critical-to-quality sensor performance output variability with respect to process and environmental inputs.
• Apply and interpret characterization DOE models to establish optimal material and process input set points with respect to sensor in-vivo performance.
• Apply data analysis and statistical methodologies to generate insights on sensor performance and develop transfer functions.
• Serve as subject matter expert and primary contact for specific projects and initiatives.
• Ensure execution of detailed engineering analyses and documentation to support design development and process transfer.
• Work with engineers and technicians to execute experimental designs and analysis.

Technical Qualifications

• Bachelor's degree or higher in biomedical engineering or a related field.
• Medical device industry experience with direct experience in development of biosensors.
• Experience in application of DRM methodology, Six Sigma, Lean, and DMAIC for product design and continuous improvement.
• Experience with statistical analysis of data using tools such as Minitab, JMP, and MATLAB, including T-test, ANOVA, gage R&R, and process capability analysis.
• Direct experience with MATLAB and Python, and experience with signal processing and interpretation of biosensing signals.
• Knowledge of in-vitro and in-vivo testing of subcutaneous medical devices, regulatory submissions, and guidance for medical devices.
• Experience with technical documentation including laboratory notebooks, engineering reports, SOPs, test protocols, and IQ, OQ, PQ procedures.
• Self-driven, detail-oriented, and able to work independently and within a team-based environment with strong project management skills.

The Biomedical Engineer owns field installation, preventive maintenance, and emergency repair of clinical diagnostic instrumentation for a leading clinical laboratory marketplace manufacturer specializing in hematology, cancer, and colorectal cancer screening products. Reporting to field service management and serving hospital and laboratory customers nationwide, this role delivers the technical uptime and customer training that sustains product performance and client satisfaction.

Role Responsibilities

• Travel to customer sites to install, train, troubleshoot, repair, and perform preventive maintenance on all company diagnostic instrumentation on-site and off-site.
• Provide high quality phone support responding to customer inquiries, technical support, and customer training on operation, maintenance, and troubleshooting.
• Work on new test systems, make recommendations, and assist in developing and writing test procedures, standard operations protocol, and training material.
• Maintain self-motivation and operate with minimum supervision while functioning as a team player.
• Participate in on-call scheduling including occasional 24/7 availability a few times per year.

Professional Experience

• Bachelor's degree in electrical engineering or biomedical engineering preferred, or equivalent experience in medical technology.
• 3-5 years of experience servicing clinical diagnostic and laboratory equipment.
• Strong knowledge of medical instrument systems technology including mechanical, electrical, and fluidics, with knowledge of chemistry and software as a plus.
• Strong knowledge of lab equipment and tools such as soldering irons, digital volt meters, power supplies, and temperature measurement equipment.
• Ability to disassemble, troubleshoot, and reassemble instrument sub-assemblies, and solve complex mechanical and system problems using technical manuals and engineering support.
• Proficient in Microsoft Office and computer-based tools for reports, email, and general communication.
• Excellent communication, organizational, and problem-solving skills with the ability to interface with customers and associates professionally.

Embedded within a shared services biomedical team, the Biomedical Engineer performs scheduled and corrective repairs, inspections, and electrical safety testing across a broad range of medical equipment and systems in compliance with applicable codes. Working closely with biomedical specialists across instrumentation, imaging, nuclear medicine, clinical laboratory, and clinical systems integrations, as well as OEM representatives and business partners, this role ensures continuous equipment availability across multi-site healthcare operations.

Job Functions

• Perform all phases of scheduled and corrective repairs of biomedical equipment and medical systems under the supervision of a manager or designee.
• Perform pre-issue and asset accounting, equipment installation and de-installation as needed.
• Perform scheduled and unscheduled inspections, maintenance, and electrical safety tests of biomedical equipment to maintain code compliance.
• Document the results of all inspections, maintenance, and tests in a timely manner.
• Collaborate with biomedical engineers across all specialties including instrumentation, X-Ray, CT and MR, clinical laboratory, and clinical systems integrations, as well as KPIT, business partners, and OEM representatives.
• Travel frequently to provide service support, attend technical training, and complete after-hours and on-call work as scheduled.

Position Requirements

• High school diploma or GED required, with an associate degree or equivalent in electronics, physics, or a related science preferred.
• Minimum 4 years of formal and on-the-job training experience with medical equipment and systems in the assigned specialty area.
• Valid unrestricted Class C or better driver's license with a good driving record required.
• Proficient in operating PCs with Windows operating systems.
• Willingness to work extended hours and participate in weekday and weekend on-call schedules for emergency service.

Reporting to a hospital supervisor, the Biomedical Engineer manages the complete lifecycle of medical equipment across the hospital campus, covering technology review, installation, repair, safety alert monitoring, and disposal management. Partnering with clinical and engineering stakeholders and providing on-call support outside office hours, this role safeguards equipment reliability and patient safety within a leading private teaching hospital environment.

Day-to-Day Responsibilities

• Assist the team in managing the total lifecycle of medical equipment used within the hospital campus, including technology review, installation.
• Commissioning, repair and maintenance, safety alert monitoring.
• Replacement planning, and disposal management.
• Perform ad-hoc duties assigned by supervisor.
• Provide on-call support during off-office hours.

Knowledge Skills and Abilities

• Degree majoring in engineering, biomedical or equivalent.
• At least 5 years of working experience relating to the medical device industry, preferably in a hospital setting.
• Strong technical know-how in the medical device area.
• Fluent in written and spoken English and Chinese.
• Excellent communication and coordination skills with a positive attitude and fast learning ability.
• Good team player.

vThe Biomedical Engineer delivers software and hardware engineering research support for the Combat Casualty Care mission, developing instrumentation, control algorithms, and standardized testing platforms within the Engineering, Technology, and Automation Combat Research Team. Collaborating with research program officials and contributing to at least two publishable findings annually, this role advances automated medical device systems including smart tourniquet and augmented reality technologies that directly improve battlefield casualty outcomes.

Engineering Responsibilities

• Enrich practices, techniques, and knowledge in medical, physiological, and biological sciences.
• Enhance and ensure the health, safety, and welfare of living systems including human and animal.
• Create and improve designs, instrumentation, materials, diagnostic and therapeutic devices, medical systems, and other devices needed in the study and practice of medicine.
• Assist with the development of standardized testing platforms to provide objective, data-based conclusions for answering research hypotheses.
• Develop models using simulators, cadavers, and large animals to test the efficacy of developing devices.
• Perform data acquisition for clinical applications using Python, image processing and analysis for automated image recognition systems, and develop control systems and algorithms for medical applications.
• Conduct statistical analysis, assist with writing patent documentation, and develop documentation for software and medical devices.
• Contribute to at least 2 publishable research findings annually in the form of abstracts, papers, presentations, or posters.

Experience and Qualifications

• Bachelor's degree in biomedical, mechanical, or electrical engineering or a related field.
• Minimum 3 years of experience in biomedical engineering or a clinical environment including development of experimental devices and systems.
• Development experience using tools such as MATLAB, CAD, SolidWorks, and FEA simulations.
• Expert computer skills with advanced knowledge of Microsoft Office Suite.
• Strong written and verbal communication, leadership, and interpersonal skills.
• Strong organizational skills with attention to detail and ability to coordinate multiple projects simultaneously.

Sitting at the intersection of biomedical engineering and diagnostic innovation, the Biomedical Engineer designs and executes experiments, analyzes data using Python or R, and contributes to next-generation device development within Cytovale's quality management system. Operating alongside an interdisciplinary team of biologists, data scientists, and engineers focused on rapid-response disease screening, this role enables faster, more accurate clinical decision-making for critically ill patients.

What You'll Do

• Design and execute experiments using Cytovale's diagnostic device.
• Analyze data in Python or R and apply appropriate statistical methods to interpret results and form independent conclusions.
• Independently manage projects from planning to results.
• Write protocols, work instructions, and report results in compliance with Cytovale's QMS.
• Contribute to the design and development of next generation devices.

Qualifications and Experience

• Master's degree in biomedical engineering or a related field, or bachelor's degree with 1+ years of work experience in medical device or diagnostic development.
• Experience in design of experiments including applied statistics required.
• Expertise in microfluidics and plastic consumables design and manufacturing experience desired.
• Knowledge of CFR 820.30 and ISO 14971 preferred.
• Proficient in Python or equivalent coding tools.
• Fast learner with a can-do attitude and ability to work independently in a high-velocity startup environment.
• Excellent communicator, detail-oriented, and an avid GDP and GLP laboratory practitioner.

Biomedical Engineer manages routine and emergency field servicing of Randox analysers and associated equipment, covering preventive maintenance, installation, commissioning, and remote technical support for customers across the United States. The work directly supports customer uptime and satisfaction by building deep product knowledge, maintaining accurate service records, and delivering responsive on-site and telephone technical assistance from a home office base.

Scope of Work

• Perform routine servicing and preventative maintenance of analysers and associated equipment in the field.
• Perform emergency breakdown repair of analysers in the field.
• Maintain service and maintenance records according to Service Department procedures.
• Install, commission, and set up analyser equipment.
• Provide technical support by telephone and email to Randox customers and provide technical support for analyser development.
• Build and maintain extensive knowledge of Randox analysers and associated equipment.

Required Qualifications

• Relevant engineering qualification or equivalent accredited apprenticeship.
• Experience in medical instrumentation, engineering, and computer software.
• Experience in clinical chemistry and applications knowledge.
• Ability to operate and repair various analysers and analytical instrumentation and record analytical data correctly.
• Highly motivated with the ability to work independently and travel extensively.
• Excellent communication and organisational skills with the ability to effectively establish and maintain good working relationships with internal departments and customers.
• Must hold a full driving licence and be computer literate.