Agent/ Attorney Address Line 1:8300 Greensboro Drive
Agent/ Attorney Address Line 2:Suite 550
Agent/ Attorney City:McLean
Agent/ Attorney State/ Province:VIRGINIA
Agent/ Attorney Country:UNITED STATES OF AMERICA
Agent/ Attorney Postal Code:22102
Agent/ Attorney Email:kvongsavanh@bal.com
Position Info
Prevailing Wage Track Number:P10020342940369
Prevailing Wage SOC Code :11-9199
Prevailing Wage SOC Title :Compliance Manager
Prevailing Wage Skill Level:Level III
Prevailing Wage:133806
Prevailing Wage Unit of Pay:Year
Prevailing Wage Source:OES
Prevailing Wage Other Source:
Prevailing Wage Determination Date :2021-05-27
Prevailing Wage Expiration Date :2021-08-25
Wage Offer From:133806
Wage Offer To:143806
Wage Offer Unit of Pay:Year
Workstie Address Line 1:5010 Cheshire Parkway
Worksite Address Line 2:Suite 2
Worksite City :Plymouth
Worksite State:MINNESOTA
Worksite Postal Code:55446
Job Title:Staff Compliance Auditor
Minimum Education:Bachelor's
Other Degree/ Diploma:
Major Field of Study:See H.14
Required Training:N
Required Training Month:
Required Field of Training:
Required Experience :Y
Required Expreience Months :48
Accept Alternate Field of Study:N
Accept Alternate Major:
Alternate Combination of Education/ Experience:N
Required Alternate Level of Education :
Other Alternate Level of Education:
Acceptable Years of Experience:
Accept Foreign Educationa:Y
Acceptable Alternate Occupation:Y
Acceptable Alternate Occupation Month:48
Accept Alternate Job Title:Related Occupation
Normal Requirements of Job Opportunity:N
Required Foreign Language:N
Specific Skills:Employer will accept Bachelors degree in Science, Engineering, or a related field and four years of work experience in job offered or four years of work experience in a related occupation. Experience may be gainedbr concurrently. Any suitable combination of education, training, or experience is acceptable. Education or experience must includebr 1 4 years of experience in the Medical Device Industry;br 2 Experience with ETQ Excellence Through Quality application;br 3 Experience with Medical Device Directive 9342EEC;br 4 Experience with ISO 13485 and 21CFR Part 820;br 5 Experience with EU MDR 201745;br 6 Experience with CFDA Order No. 64 Good Manufacturing Practices GMPs for Medical Devices;br 7 Reporting tool experience and training, including Qlik and data analysis used to escalate trending issues to upper management; and,br 8 Experience with Microsoft Office.