QA Document Control Associate Manager MacroGenics
THIS JOB HAS EXPIRED
Location: Rockville, MD
Applicants must meet the following requirements:
Bachelor?s degree
Minimum of 7 to 10 years in a cGMP manufacturing environment
Previous document control experience in a cGMP manufacturing environment is required
In-depth knowledge and proficiency with personal computers is a must
Experience with TrackWise Quality Management System is a plus
Must be able to handle multiple priorities at once
Must be able to work independently with minimal supervision
The selected candidate will be responsible for:
Management and oversight of GXP documentation to ensure timely processing
Management and oversight of GXP training program and electronic training records
Management and oversight of the GXP document control program to ensure compliance
Writing new or revising existing SOPs, as appropriate
Maintenance of SOP binders and electronic versions of SOPs on company intranet
Maintenance of document templates on company intranet
Organizing and chairing quarterly training status meetings
Oversight and maintenance of GXP controlled document room
Scanning and filing of GXP documents
Issuance of manufacturing batch records and protocols
Organizing and filing master SOPs, manufacturing batch records, and batch release test data
Organizing and filing protocols and reports
Management of direct report(s)
Assisting with special QA projects and other duties, as assigned
Benefits: Competitive salary and benefits package
Qualified applicants, please use the following link to apply:
http://macrogenics.balancetrak.com/0141201
| Location: |
1500 East Gude Drive
Rockville, MD 20850
United States
|
THIS JOB HAS EXPIRED