Consulting
Noblitt & Rueland Noblitt & Rueland Irvine, CA Irvine, CA Estimated:
$61.
5K - $77.
8K a year Estimated:
$61.
5K - $77.
8K a year 2 hours ago 2 hours ago 2 hours ago Noblitt & Rueland provides specialized consulting services for our clients.
We are in need of additional high quality consulting resources to handle demand or perform specialized tasks.
Noblitt & Rueland requires the highest quality consultants that have a great deal of practical experience in the services they offer Noblitt & Rueland 5405 Alton Parkway 5A, #530 Irvine, CA 92604-3718 All correspondence will be kept confidential.
Areas/Items of Interest:
Submissions- 510k, PMA, IDEs, De Novo, CE Mark Clinical Evaluation Reports (CERs) Auditors:
FDA 21 CFR Part 820, ISO 13485, MDSAP, etc.
Quality System Implementation & Auditing (FDA QSR/GMP, 13485) Ex-FDA:
Mock Inspections, Warning Letter & FDA-483 remediation Design Control Implementation & Auditing Risk Management/hazard analysis/ISO 14971 Implementation & Auditing International/Global Country Specific Regulatory Compliance (please detail the countries; i.
e.
Japan, China, Brazil, etc) Software Quality Assurance Software Verification & Validation Software Development (describe languages and platforms, embedded processors & PCs) Hardware Design (digital & analog) Regulatory Affairs-Medical Device & Pharmaceutical Industry Proficiency in writing lifecycle procedures (SOPs) Multi-lingual experience on Regulatory Submissions & Quality Systems.
Estimated Salary: $20 to $28 per hour based on qualifications.
$61.
5K - $77.
8K a year Estimated:
$61.
5K - $77.
8K a year 2 hours ago 2 hours ago 2 hours ago Noblitt & Rueland provides specialized consulting services for our clients.
We are in need of additional high quality consulting resources to handle demand or perform specialized tasks.
Noblitt & Rueland requires the highest quality consultants that have a great deal of practical experience in the services they offer Noblitt & Rueland 5405 Alton Parkway 5A, #530 Irvine, CA 92604-3718 All correspondence will be kept confidential.
Areas/Items of Interest:
Submissions- 510k, PMA, IDEs, De Novo, CE Mark Clinical Evaluation Reports (CERs) Auditors:
FDA 21 CFR Part 820, ISO 13485, MDSAP, etc.
Quality System Implementation & Auditing (FDA QSR/GMP, 13485) Ex-FDA:
Mock Inspections, Warning Letter & FDA-483 remediation Design Control Implementation & Auditing Risk Management/hazard analysis/ISO 14971 Implementation & Auditing International/Global Country Specific Regulatory Compliance (please detail the countries; i.
e.
Japan, China, Brazil, etc) Software Quality Assurance Software Verification & Validation Software Development (describe languages and platforms, embedded processors & PCs) Hardware Design (digital & analog) Regulatory Affairs-Medical Device & Pharmaceutical Industry Proficiency in writing lifecycle procedures (SOPs) Multi-lingual experience on Regulatory Submissions & Quality Systems.
Estimated Salary: $20 to $28 per hour based on qualifications.
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