What Jobs are available for Medical Technology in Bahrain?
Showing 12 Medical Technology jobs in Bahrain
Senior Research Scientist - Biomedical Engineering
Posted 1 day ago
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Job Description
Responsibilities:
- Lead and conduct advanced research projects in biomedical engineering.
- Design, implement, and troubleshoot complex experiments.
- Analyze and interpret experimental data, drawing scientifically sound conclusions.
- Develop novel technologies, devices, or methodologies within the scope of biomedical research.
- Write and submit grant proposals to secure research funding.
- Publish research findings in high-impact peer-reviewed journals.
- Present research at national and international scientific conferences.
- Collaborate effectively with cross-functional research teams and external partners.
- Mentor junior researchers and contribute to their professional development.
- Stay abreast of the latest advancements and emerging trends in biomedical engineering.
- Ph.D. in Biomedical Engineering or a closely related scientific discipline.
- Minimum of 7 years of post-doctoral research experience in biomedical engineering.
- Proven track record of leading research projects and securing extramural funding (grants).
- Strong publication record in reputable scientific journals.
- Expertise in one or more specialized areas of biomedical engineering (e.g., medical imaging, tissue engineering, biomechanics, drug delivery).
- Proficiency in relevant research techniques and instrumentation.
- Excellent data analysis and statistical interpretation skills.
- Strong written and verbal communication skills for scientific reporting and presentation.
- Ability to work independently and manage research timelines effectively in a remote setting.
- Demonstrated ability to innovate and solve complex scientific problems.
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Senior Scientific Researcher - Biomedical Engineering
Posted 12 days ago
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Job Description
Key Responsibilities:
- Lead the design and execution of complex research projects in biomedical engineering, focusing on areas such as medical device innovation, biomaterials, tissue engineering, or medical imaging.
- Develop and validate new experimental methodologies and protocols.
- Conduct rigorous data analysis, interpretation, and reporting of research findings.
- Collaborate closely with cross-functional teams, including engineers, biologists, clinicians, and statisticians.
- Author peer-reviewed publications in high-impact scientific journals.
- Prepare and present research findings at national and international conferences.
- Contribute to the development of patent applications and intellectual property.
- Stay current with the latest advancements and emerging trends in biomedical engineering and related scientific fields.
- Mentor junior researchers and contribute to a collaborative and innovative research environment.
- Manage research budgets and resources effectively.
Qualifications:
- Ph.D. in Biomedical Engineering, Mechanical Engineering, Electrical Engineering, or a related discipline with a biomedical focus.
- Minimum of 7 years of post-doctoral research experience in biomedical engineering.
- Demonstrated expertise in designing and conducting advanced experimental research.
- Strong proficiency in data analysis software (e.g., MATLAB, R, Python) and statistical methods.
- Proven publication record in leading peer-reviewed journals.
- Excellent written and verbal communication skills, with the ability to clearly articulate complex scientific concepts.
- Experience with grant writing and funding applications is a plus.
- Ability to work independently, manage multiple research priorities, and thrive in a fully remote setting.
- Familiarity with regulatory affairs and product development processes in the medical device industry is advantageous.
- Strong problem-solving skills and a creative approach to scientific inquiry.
This is a unique opportunity for a dedicated researcher to drive innovation and make a tangible impact in the field of biomedical engineering, all within a flexible remote work structure. If you are passionate about scientific discovery and its application to healthcare, we encourage you to apply.
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Senior Research Scientist - Biomedical Engineering
Posted 18 days ago
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Job Description
Responsibilities:
- Design, conduct, and manage innovative research projects in biomedical engineering, aligning with the institution's strategic goals.
- Develop and validate novel experimental techniques, methodologies, and technologies.
- Analyze complex experimental data, interpret results, and draw meaningful conclusions.
- Author high-impact research publications for peer-reviewed journals and present findings at international conferences.
- Lead efforts in securing external research funding through grant applications and proposals.
- Supervise and mentor postdoctoral fellows, graduate students, and research assistants.
- Collaborate with cross-functional teams, including clinicians, biologists, chemists, and engineers, to foster interdisciplinary research.
- Ensure adherence to all laboratory safety protocols, ethical guidelines, and regulatory requirements.
- Contribute to the development of intellectual property and potential commercialization pathways.
- Stay abreast of the latest scientific literature and technological advancements in biomedical engineering.
- Contribute to the strategic planning and direction of the research group.
- Ph.D. in Biomedical Engineering, Mechanical Engineering, Electrical Engineering, Materials Science, or a closely related field.
- A minimum of 5-7 years of post-doctoral research experience in a relevant area of biomedical engineering.
- Demonstrated track record of independent research, evidenced by a strong publication record in reputable journals and a history of successful grant funding.
- Expertise in at least one key area of biomedical engineering (e.g., medical device design, regenerative medicine, biomechanics, drug delivery systems, biosensors).
- Proficiency in relevant research methodologies, experimental design, and data analysis techniques.
- Strong understanding of scientific principles and advanced engineering concepts.
- Excellent written and verbal communication skills, with the ability to present complex scientific information clearly and concisely.
- Proven leadership and mentorship abilities.
- Experience with computational modeling and simulation (e.g., FEA, CFD) is a plus.
- Ability to thrive in a highly collaborative, remote research environment.
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Graduate Research Assistant - Biomedical Engineering
Posted 18 days ago
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Job Description
Key Responsibilities:
- Assist in the design and execution of research experiments.
- Collect, record, and analyze experimental data meticulously.
- Operate and maintain laboratory equipment and instruments.
- Prepare research materials, solutions, and samples.
- Conduct literature reviews to support research projects.
- Contribute to the writing of research papers, reports, and presentations.
- Maintain a clean and organized laboratory workspace.
- Follow all laboratory safety protocols and procedures.
- Collaborate effectively with research team members.
- Present research findings at lab meetings and potentially at conferences.
Qualifications:
- Currently enrolled in a Master's or PhD program in Biomedical Engineering, Mechanical Engineering, Electrical Engineering, or a closely related field.
- Strong academic record with a GPA of 3.5 or higher.
- Basic understanding of research methodologies and experimental design.
- Familiarity with laboratory techniques and equipment relevant to biomedical research.
- Excellent attention to detail and organizational skills.
- Ability to work independently and as part of a team.
- Good written and verbal communication skills.
- Enthusiasm for scientific research and a willingness to learn.
- Previous research experience is a plus.
- Proficiency in basic data analysis software (e.g., Excel) is beneficial.
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Principal Lecturer in Biomedical Engineering
Posted 24 days ago
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Job Description
Key Responsibilities:
- Deliver high-quality lectures, tutorials, and laboratory sessions across a range of Biomedical Engineering modules.
- Develop and update course curricula to reflect the latest advancements and industry demands.
- Supervise undergraduate and postgraduate research projects and dissertations.
- Conduct independent research, secure external funding, and publish findings in leading academic journals.
- Contribute to the departmental administration and strategic planning.
- Mentor and support students, providing academic and career guidance.
- Engage in collaborative research initiatives within the university and with external partners.
- Promote the department and university through outreach activities and professional engagement.
- Uphold the highest standards of academic integrity and teaching excellence.
- Participate in quality assurance processes and external reviews.
Qualifications:
- Ph.D. in Biomedical Engineering or a closely related discipline.
- A strong record of teaching experience at the university level, with demonstrated excellence in pedagogy.
- A significant publication record in reputable peer-reviewed journals and conference proceedings.
- Evidence of successful grant applications and research funding acquisition.
- Expertise in one or more key areas of Biomedical Engineering, such as biomaterials, biomechanics, medical imaging, or tissue engineering.
- Excellent communication, presentation, and interpersonal skills.
- Proven ability to lead and motivate students and research teams.
- Experience in curriculum development and academic leadership.
- Professional registration or chartered status with a relevant engineering body is desirable.
- Commitment to continuous professional development.
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National Sales Director - Medical Devices
Posted 2 days ago
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Regional Sales Director (Medical Devices)
Posted 18 days ago
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Job Description
Responsibilities include developing and executing regional sales strategies, setting performance goals for the sales team, and ensuring consistent achievement of quotas. You will be responsible for recruiting, training, coaching, and motivating sales representatives to reach their full potential. Building and maintaining strong relationships with key opinion leaders, hospital administrators, and procurement departments will be paramount. Market analysis, competitor intelligence gathering, and strategic account planning will be critical components of this role. You will also collaborate closely with marketing, product management, and clinical support teams to ensure a cohesive go-to-market strategy. Accurate sales forecasting, budget management, and comprehensive reporting to senior leadership are essential. The ability to navigate complex healthcare regulations and reimbursement landscapes is a significant advantage. This position demands strong analytical skills, strategic vision, and a passion for improving patient care through innovative medical technologies. You will be a key driver of our client's success in the region.
Qualifications:
- Bachelor's degree in Business, Marketing, or a related healthcare field; MBA preferred.
- 10+ years of progressive experience in medical device sales, with a minimum of 5 years in sales management or leadership.
- Proven track record of exceeding sales targets in a competitive market.
- Strong understanding of the healthcare ecosystem, including hospitals, clinics, and distributor networks.
- Excellent leadership, communication, negotiation, and strategic planning skills.
- Experience in market analysis and competitor benchmarking.
- Ability to work effectively in a hybrid setting, requiring both remote work and on-site presence for team leadership and client engagement.
- Familiarity with relevant medical device regulations and compliance standards.
- Strong network within the healthcare sector is a significant asset.
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Senior Quality Assurance Manager - Medical Devices
Posted 4 days ago
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Job Description
Responsibilities:
- Develop, implement, and maintain the company's Quality Management System (QMS) in accordance with relevant regulatory standards (e.g., ISO 13485, FDA 21 CFR Part 820).
- Lead and manage the QA team, including performance management, training, and professional development.
- Oversee all quality assurance activities, including document control, change management, CAPA (Corrective and Preventive Actions), and internal audits.
- Conduct regular internal audits and support external audits by regulatory agencies and notified bodies.
- Ensure product conformity and compliance throughout the product lifecycle, from design and development to post-market surveillance.
- Review and approve product documentation, validation reports, and manufacturing batch records.
- Manage supplier quality, including qualification, auditing, and performance monitoring.
- Investigate and resolve quality issues, implementing effective corrective and preventive actions.
- Champion quality principles and foster a quality-conscious culture across all departments.
- Stay up-to-date with evolving regulatory requirements and industry best practices in medical device quality assurance.
- Bachelor's degree in Engineering, Science, or a related technical field. Advanced degree or relevant certifications (e.g., ASQ Certified Quality Engineer) are a strong plus.
- A minimum of 7 years of experience in quality assurance within the medical device or pharmaceutical industry.
- In-depth knowledge of ISO 13485, FDA QSR (21 CFR Part 820), and other relevant international quality standards.
- Proven experience in developing and managing QMS documentation and procedures.
- Demonstrated experience in leading audits, managing CAPA systems, and conducting risk assessments.
- Strong leadership, team management, and motivational skills.
- Excellent analytical, problem-solving, and decision-making abilities.
- Exceptional communication, interpersonal, and influencing skills.
- Proficiency in quality tools and software.
- Ability to work effectively in a hybrid environment, balancing on-site collaboration with remote responsibilities.
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Senior Quality Assurance Engineer, Medical Devices
Posted 5 days ago
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Job Description
Key responsibilities include developing and executing comprehensive quality control plans, conducting risk assessments, and validating manufacturing processes. You will be responsible for the investigation of non-conformances, root cause analysis, and the implementation of corrective and preventive actions (CAPA). The Senior QA Engineer will ensure compliance with international quality standards such as ISO 13485 and FDA regulations. You will work closely with R&D, manufacturing, and regulatory affairs teams to ensure that product designs and processes are robust and meet all applicable requirements. This role also involves preparing for and participating in internal and external audits. The ability to interpret technical specifications, engineering drawings, and test protocols is essential. Strong leadership, communication, and problem-solving skills are required to guide QA processes and mentor junior team members.
Qualifications:
- Bachelor's degree in Engineering (Mechanical, Electrical, Biomedical) or a related scientific field.
- Minimum of 5-7 years of experience in Quality Assurance within the medical device industry.
- In-depth knowledge of quality management systems (QMS), such as ISO 13485 and FDA 21 CFR Part 820.
- Proven experience with risk management principles (e.g., ISO 14971).
- Demonstrated experience in validation and verification activities (IQ, OQ, PQ).
- Strong understanding of manufacturing processes and statistical quality control.
- Excellent analytical and problem-solving skills, with a strong attention to detail.
- Proficiency in developing and implementing CAPA systems.
- Effective communication and interpersonal skills, with the ability to collaborate across departments.
- Experience preparing for and participating in regulatory audits.
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Senior Quality Assurance Manager - Medical Devices
Posted 15 days ago
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Job Description
Key Responsibilities:
- Develop, implement, and maintain the company's Quality Management System (QMS) in compliance with relevant regulations (e.g., ISO 13485, FDA 21 CFR Part 820).
- Oversee all aspects of QA operations, including document control, change control, CAPA, audits, and risk management.
- Lead internal and external audits, ensuring regulatory compliance and identifying areas for improvement.
- Manage the complaint handling and adverse event reporting processes.
- Develop and execute validation and verification protocols for software and hardware components.
- Collaborate with R&D, Engineering, Manufacturing, and Regulatory Affairs teams to ensure quality is integrated throughout the product lifecycle.
- Establish quality metrics and key performance indicators (KPIs), monitoring trends and implementing corrective actions.
- Provide training and guidance to personnel on QMS requirements and quality best practices.
- Lead continuous improvement initiatives to enhance product quality and process efficiency.
- Review and approve product release documentation.
- Manage supplier quality and conduct supplier audits.
- Represent the company during regulatory inspections.
- Effectively manage and mentor a remote QA team, fostering a culture of quality excellence.
Qualifications:
- Bachelor's degree in Engineering, Science, or a related technical field. A Master's degree is preferred.
- Minimum of 8 years of progressive experience in Quality Assurance within the medical device industry.
- Extensive knowledge of ISO 13485, FDA 21 CFR Part 820, and other relevant medical device regulations.
- Proven experience in developing and maintaining a comprehensive QMS.
- Strong understanding of product development lifecycle for medical devices.
- Experience with risk management (ISO 14971) and CAPA processes.
- Excellent analytical, problem-solving, and decision-making skills.
- Demonstrated leadership and team management abilities, particularly in a remote setting.
- Exceptional communication, interpersonal, and documentation skills.
- Proficiency in quality management software and tools.
- Ability to work independently and manage multiple priorities in a fast-paced environment.
- Proficiency in English; knowledge of other languages is a plus.
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