Vadodara, Gujarat, India
$40/hr · Starting at $100
Technical file preparation and review of medical device as per EUMDR 2017/745, gap assessment of QMS documents, QMS documents preparation and review for ISO 13485, 510k dossier preparation and review
Granger, Indiana, United States
$100/hr · Starting at $100
Review organizational procedures for Medical Device software life cycles, planning, design inputs, design implementation, design outputs, design verification, design validation, design change, and des…
Crestwood, Kentucky, United States
$120/hr · Starting at $25
25 YEARS IN PRODUCT DEVELOPMENT (R&D), QUALITY ASSURANCE, REGULATORY AND MANUFACTURING (MEDICAL DEVICES, COMBINATION PRODUCTS AND PHARMA) Results driven leader and contributor at any level capable of
Kolkata, West Bengal, India
$10/hr · Starting at $25
I am a postgraduate (M.Pharma), having 10 years of experience in quality assurance and regulatory affairs field of Pharma and Medical Devices. Currently I am working as a quality and Regulatory Affai…
Jyothinagar, Telangana, India
$20/hr · Starting at $300
Medical Device development from Scratch. Whether it may be Class 1, class 2 or class 3 medical device. I help you set up a process for making a final device. Help you with the machine design, product
Dhaka, Dhaka, Bangladesh
$20/hr · Starting at $25
Over the last 4 years, I have worked on various data entry, ad-hoc projects being meticulous about details and accuracy.My core competencies lies in Data Extractions for Medical Companies, Web Researc…
Zichron Y'aakov, HaZafon, Israel
am a regulatory affairs consultant in Israel. I can prepare submissions to the Israeli Ministry of health in a professional manner. I worked for a global medical device company for 13 years(Covidien n…
Surat, Gujarat, India
$25/hr · Starting at $25
Professional Summary Strongly reliable and focused Regulatory Affairs Specialist with great depth and breadth of experience in medical device review and evaluation. Superb multitasker able to handle m…
Asheville, North Carolina, United States
$30/hr · Starting at $3,000
Development and test for new FDA regulated medical devices including functional test procedures (FCT) for troubleshooting of components, subassemblies, and assemblies as well as supporting development…
lagos, Lagos State, Nigeria
$500/hr · Starting at $1,500
Welcome... Hakande3D Medical Animation Studio specializes in delivering concise and lucid scientific concepts with technical and medical accuracy through 3D medical illustration and animation. Our tea…
Jacksonville Beach, Florida, United States
Past Earnings
$125/hr · Starting at $35
Provides medical device manufacturers expert guidance in meeting global medical device regulatory compliance such as, US FDA and CE Marking. Experience in developing ISO 13485, FDA QSR, cGMP, CMDCAS,…
Pimpri, Pune, Maharashtra, India
ID Verified
$15/hr · Starting at $3,000
We provide service to set up the medical device manufacturing unit, right from design through clean room, quality management system set up, Indian FDA licensing, CE marking and till USFDA.
Hyderabad, Telangana, India
$35/hr · Starting at $25
Expert in Pharmaceuticals medical devices, pharmaceutical and analytical equipments and device marketing and market research,Healthcare Marketing Analysis,
Bengaluru, Karnataka, India
$20/hr · Starting at $200
Automotive engineering, Medical Device, Hydraulic systems, Material selection, Testing, Design Solution, FMEA.
Ljubljana, Ljubljana, Slovenia
$40/hr · Starting at $25
My work experiences are connected with following skills: CAD design, medical devices, embedded design, supply chain managing, compliance and certification, product development, biosensors (electroche…
Lupton City, Tennessee, United States
$40/hr · Starting at $500
I am a mechanical engineer with over a decade in the healthcare field. For a large portion of that time, I've been a medical device product development engineer with exposure to the full development l…
Maidenhead, England, United Kingdom
$115/hr · Starting at $1,000
A dedicated Compliance Director and Data Protection professional, specialising in Artificially Intelligent Medical Device Software, their Global Regulations, Quality and Data Protection requirements.
Surrey, British Columbia, Canada
$12/hr · Starting at $50
Verification Validation DHF Remediation Quality Engineering GD&T Failure Mode and Effect Analysis ISO 13485
Brymbo, Clwyd, United Kingdom
$150/hr · Starting at $1,000
Specialists in the development of software for medical devices, creation of software development processes and documentation and conducting audits. Experts in the application of IEC62304 and ISO14971
Rockwall, Texas, United States
$180/hr · Starting at $5,000
I have designed new products, and managed product design teams. I have managed projects with multi-million dollar budgets that have added multiple millions in revenue once launched. I have managed eve…