san leandro, California, United States
$100/hr · Starting at $25
FDA audit and remediation of DHF and DMR. Identify gaps in documentation (ISO 13485 and QSR). Verification and validation, process validation, risk analysis, risk management (ISO 14971).
Palm Beach Gardens, Florida, United States
$90/hr · Starting at $25
Quality, Regulatory Affairs and Compliance Consultant for the medical device, life science, fields..
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…
Kavindapadi, Tamil Nadu, India
$10/hr · Starting at $30
I have Experience and well knowledge Quality Engineer and i have familiar MS office Power point ,Word,excel etc..i have knowledge in quality management system also
Vellookkara, Kerala, India
$5/hr · Starting at $25
2D drawings-AutoCAD, s3D Modeling-Solid works, ISO document preparation, knowledge about ISO 13485:2016
Dubai, Dubai, United Arab Emirates
$15/hr · Starting at $200
An exceptional and resourceful Quality Assurance Professional who focused on Quality & Safety Management Operations, Quality Systems Compliance and International Standards Certification, Policies & Pr…
New Delhi, Delhi, India
$30/hr · Starting at $120
We are in consulting in last 16 year and have executed more than 700 projects and trained more than 7000 people Offering consulting for business excellence ,process mapping and improvement, iso 9001;A…
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
Bengaluru, Karnataka, India
$40/hr · Starting at $40
Medical Device Design And Development Innovative Device Design and Development concept development QMS implementation DMF Documentation based on design support on existing medical device development p…
Basingstoke, Hampshire, United Kingdom
$18/hr · Starting at $250
Development, research and review of scientific and technical devices and systems used in medicine, health care, rehabilitation and sports.
Miskolc, Borsod-Abauj-Zemplen, Hungary
$25/hr · Starting at $50
Quality management expert, medical device company, dental implants Prepare the company for audit. Preparing technical documentation, and SOP-s.
Bhiwandi, Maharashtra, India
I am experienced data entry operator. I can complete any project perfectly. I have completed more project.
Kochi, Kerala, India
I am working as a management consultant since 2004 and have 16 years of experience in the related field which specialized in the documentation and implementation of ISO 9001,ISO 14001,ISO 22000,ISO 13…
San Jose, California, United States
$225/hr · Starting at $100
I am a software validation expert with 17 year experience in the medical device industry. My specialty includes but is not limited to: software gap analysis & review, new and modified software valida…
$40/hr · Starting at $30
List of Offerings: Regulatory Services ● Product Regulatory Strategy Support ● USFDA510(k)Submissions ● Device Listing and Facility Registration ● CE marking as per EU MDR for Class I, IIa, IIb an…
ID Verified
$20/hr · Starting at $25
A B. Tech Mechanical Engineer offering 6 years of product-development & designing solutions in Medical Devices products. Notable Clients for which product development-engineering services were offered…
Antioch, Illinois, United States
$35/hr · Starting at $25
Professional Summary Areas of Expertise Technical Summary • AutoCAD Inventor • SolidWorks 2005 – 2016, AutoCAD 2013 • Minitab • Knowledge of GMPs, FDA guidelines, purchasing practices and process val…
Londrina, Parana, Brazil
$15/hr · Starting at $300
More than 2 years studying Project management at Pitagoras University. Managed and executed 5 projects for a CSSD products importer and distributor. English Fluent Portuguese Fluent Spanish intermedia…
Thousand Oaks, California, United States
I am an expert in preparing companies for ISO 2001:2015, AS 9100D, and ISO 13485:2016 certification audits. I also excel in general QMS development and documentation. Second shift and weekend work is…
Ghaziabad, Uttar Pradesh, India
$50/hr · Starting at $2,500
More than 20+ yrs of experience in various areas of clinical reserach. We offfer services like: (1) Protocol Designing (2) Medical Writting (3) Data Management Plan Designing (4) Sample Size Calculati…