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With over 10 years of experience in the medical device industry, I am passionate about translating scientific research and innovation into products and services that make a tangible difference in people’s lives. My expertise spans medical device testing, validation, regulation, manufacturing, quality assurance, research and development, leadership, and collaboration.I am particularly proud to have established the first and only Canadian laboratory #SteriLabs specializing in advanced medical device testing and reprocessing validation for medical device manufacturers, hospitals, and research institutes. My contributions extend to the development of AAMI, ASTM, and ISO standards and guidance documents, where I work to shape the future of medical device safety and efficacy.As the Director of Research & Innovation at SteriPro Canada, I lead R&D projects, recruit and mentor top talent, and forge strategic partnerships that drive innovation forward. My role involves advising the executive team on research strategies, overseeing design and development plans, conducting FMEA Risk Assessments, and ensuring rigorous Design Verification and Validation Testing.My mission is to lead innovation and excellence in medical device reprocessing—a field critical to patient safety, environmental sustainability, and cost-effectiveness. I am driven by a commitment to improve healthcare outcomes through cutting-edge research and the highest standards of quality and safety.
Steripro Canada
View- Website:
- steriprocanada.com
- Employees:
- 55
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Director Of Research & InnovationSteripro Canada Feb 2020 - PresentToronto, Ontario, CanadaSteriPro is a medical device reprocessing company certified to ISO 13485 for manufacturing reprocessed single-use devices. SteriPro's offsite reprocessing model is based on using a state-of-the-art facility, optimized production processes, and qualified equipment.Main duties: • Initiate and oversee R&D work; recruit and supervise staff; identify potential collaborators; advise the executive team on research strategies and approaches. • Create and review design and development plans, FMEA Risk Assessments, Design Verification and Validation Testing, and design history files. • Oversee implementation of new medical device manufacturing processes including Design Inputs, Design Outputs, Design Verification, Design Validation, and Design Transfer per ISO 13485 and Medical Device Regulations. • Actively participating in the development of medical products related to AAMI, CSA, ASTM, and ISO standards. • Produce high-quality reports, papers, and articles of a publishable standard based on the analysis of data and literature with a clear and engaging writing style.• Represent the company during regulatory or corporate inspections and audits as well as at national and international conferences.
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Director Of OperationsSterilabs Canada Jun 2020 - PresentMississauga, Ontario, CanadaSteriLabs is a medical products testing and validation laboratory offering ISO 17025-Accredited testing services to Medical device manufacturers, Pharmaceutical companies, and Research institutes. The services include advising on materials selection and design, cleaning, disinfection, sterilization, and packaging validation testing. Testing reports are used for regulatory submissions for FDA and Health Canada approvals. Main duties: • Oversee device testing and validation laboratory services for medical device/pharmaceutical manufacturers, hospitals, and research institutes.• Leading a team of consultants, engineers, and scientists providing advisory and consulting services. • Oversee implementing and maintaining the Canadian Biosafety Standard and ISO 17025 Accreditation for Microbiology and Analytical testing laboratories. • Maximize efficiency and productivity through extensive process analysis and interdepartmental collaboration according to financial and budgetary plans. • Planning and monitoring the day-to-day running of the laboratories to ensure smooth progress
Anas Aljabo Skills
Anas Aljabo Education Details
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Postgraduate Certificate -
Regulatory Affairs Professionals Society (Raps)Certificate -
Master'S Degree, Biomaterials/Biomedical Engineering
Frequently Asked Questions about Anas Aljabo
What company does Anas Aljabo work for?
Anas Aljabo works for Steripro Canada
What is Anas Aljabo's role at the current company?
Anas Aljabo's current role is Medical Devices I Research & Development I Laboratory Testing I Quality Assurance I Regulatory Affairs.
What is Anas Aljabo's email address?
Anas Aljabo's email address is an****@****ail.com
What is Anas Aljabo's direct phone number?
Anas Aljabo's direct phone number is +4475009*****
What schools did Anas Aljabo attend?
Anas Aljabo attended Ucl, University Of Toronto, Regulatory Affairs Professionals Society (Raps), Queen Mary University Of London.
What are some of Anas Aljabo's interests?
Anas Aljabo has interest in Reactive Materials, Reading, New Technologies, Medical Technology, Health, Teaching, Education, Composites, Photography, Science And Technology.
What skills is Anas Aljabo known for?
Anas Aljabo has skills like Materials Science, Biomaterials, Research, Nanotechnology, Mechanical Testing, Medical Devices, Dental Restoration, Microbiology, Polymer Composites, Biomedical Engineering, Sterilization, Medical Device R&d.
Who are Anas Aljabo's colleagues?
Anas Aljabo's colleagues are Seleena Cordero, Wally Ranada, Eifelyn Josef - Yao, Ayra Lintag, Arun Jain, Jason Ilagan, Patricia Macatangay.
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