Since 2019, Bert Sanford has been working in Np Medical situated 266, 266. Bert is a qualified Director, Quality Assurance and Regulatory Affairs with over 14 years of work experience. According to Bert's resume and work profile, the professional has worked at more than eight companies with diverse backgrounds and gained different skills. Bert attended school at the The University of Texas at Arlington. This professional has professional certification as Six Sigma Black Belt and this professional has studied German. Bert can be found in Watertown, Massachusetts – where this person is currently located. You can search for Bert's email address and number. We can also provide you with additional contact information upon request.
Name variants:
Bertie Sanford
Last updated Jul 04, 2024
Contact Information
Workplace
Director, Quality Assurance and Regulatory Affairs
Clinton, MA
Industry
Medical Devices
Colleagues
Work History
Director, Quality Assurance and Regulatory Affairs
101 Union St, Clinton, MA 01510
from May 2019
Quality Systems and Regulatory Manager
480 Pleasant St, Watertown, MA 02472
As Quality Systems and Regulatory Manager, I'm responsible for the maintenance of the quality management system and regulatory compliance. I've revised 12 Tier 2 procedures to enhance the sy...
from Oct 2017
Manager, Quality Assurance and Quality Control
1000 Alfred Nobel Dr, Hercules, CA 94547
Responsible for the design and implementation of the Quality Management System. The system complies with ISO 13485, 21 CFR 820, and CMDR. Develop and provide training to employees on the QMS...
Dec 2014 — Sep 2017
Senior Design Assurance Engineer
110 Forbes Blvd, Mansfield, MA 02048
Responsible for: Leading the Risk Management. Design Verification and Validation, and Process Validation efforts for projects
Create Master Verification and Validation plans
Performing su...
Mar 2012 — Dec 2014
Senior Design Assurance Engineer
55 Dupont Dr, Providence, RI 02907
Responsible for: Leading the Risk Management. Design Verification and Validation, and Process Validation efforts for projects
Create Master Verification and Validation plans
Performing su...
Dec 2009 — Mar 2012
Senior Quality Compliance Engineer
Responsible for: Maintaining compliance of the quality system
Overseeing the internal audit system
Managing the Correction and Preventive Action system
Developing processes for software ...
Jul 2007 — Dec 2009
Senior New Product Development Engineer
Responsible for: Using Six Sigma tools and methods for process optimization and improvement
Completed a Black Belt project optimizing the anti-microbial impregnation process for Bactiseal®...
Oct 2005 — May 2007
New Product Release Engineer
Responsible for: Executing verification and validation protocols
Coordinating design validation and product release
Provide production line support for the MS-3 line
Review and approve d...
Oct 2003 — Oct 2005
Occupations
Executive
Director
IT Professional
Software Tester
Lawyer
Regulatory Manager
Sales Specialist
Supplier
Operations Manager
Computer Specialist
Lawyer
Services Professional
Sales Representative
Skills
Quality System
Capa
Medical Devices
Quality Assurance
V&V
Fmea
Iso 13485
Iso 14971
Design Control
Quality Auditing
Manufacturing
Product Development
Process Improvement
Engineering
Testing
Design For Manufacturing
Cross Functional Team Leadership
Injection Molding
Risk Management
Process Optimization
Process Simulation
Process Validation
Risk Assessment
Risk Analysis
Risk Mitigation
Process Mapping
Process Development
Quality Systems
Business Process Mapping
Business Process Improvement
Six Sigma
Statistical Process Control
Management
Corrective and Preventive Action
Verification and Validation
Validation
Research and Development
U.s. Food and Drug Administration
Iso Standards
Quality Control
Quality Management
Gmp
21 Cfr