Engineering - Ottawa

JOB SUMMARY
 
Documentation and auditing of new and existing internal processes.  Document management for medical device records and forms, both customer supplied and internal.
 
NATURE AND SCOPE
Duties and Responsibilities:
Quality system documentation conforming to ISO 9001 & 13485 standard
Process mapping and documentation
Internal Quality Audits
System documentation and auditing
Process documentation and auditing
Supplier Assessments
Supplier Qualifications
Other duties as required

Skills and Abilities:
Excellent organizational skills
Communication skills written and verbal
Process documentation experience
PFMEA, DFMEA, APQP & PPAP
Advanced computer skills (MS Office)
Judgment and Interpretation

EMPLOYMENT REQUIREMENTS
Educational Requirements:
Post secondary education
Years of Experience:
5 + years experience in  Quality Assurance.
5 + years experience in Quality System Audits.
Specialization Required:
Knowledge and experience with FDA Quality System Regulations for medical devices
Knowledge and experience with GMP
 
If interested please send your resume to:
 
a.cousens@maxsys.ca
 
MAX 123 

 

Position Type Contract
Application Deadline January 23, 2018
Experience Required 5+ years
Job Duration 6 months
Education Required College Diploma