Provides Administrative support by
- assisting with routine quality assurance activities
- performing administrative functions within the QA group
- supporting Quality-related Help Desk and e-mail requests
- assisting in Analytical Subcontractor documentation maintenance
Supports Data Reporting by:
- reviewing approving and releasing laboratory data
- assisting with review and approval of Certificates of Analysis and Cumulative Reports
- assisting with review and verification of Technical Reports and Summaries
Assists in Document Control by:
- issuing Master Lists numbers
- issuing Laboratory Notebooks and Logbooks
- issuing and maintaining Controlled Copies
- maintaining the Technical Library
- maintaining Archival of Records
Supports Stability activities as assigned
Supports Manufacturing activities as needed by:
- executing the quality assurance roles of batch records
- Other duties as assigned
Qualifications :
Required: a minimum of High School Diploma or Equivalent. Preferred Bachelors Degree and/or certifications in laboratory/quality/regulatory
Required: Understanding of FDA requirements and Quality Systems
Preferred: Must have good administrative skills (Microsoft Office Suite LIMS QMS)
Preferred: 1 2 Years in a laboratory environment.
Preferred: 3 years of GLP/GMP environment in laboratory operations or QA or combination of both
Additional Information :
Position is full-time Monday - Friday 8:00am - 5:00pm . Candidates currently living within a commutable distance of Cary NC are encouraged to apply.
- Excellent full time benefits including comprehensive medical coverage dental and vision options
- Life and disability insurance
- 401(k) with company match
- Paid vacation and holidays
Eurofins USA BioPharma Services is a Disabled and Veteran Equal Employment Opportunity employer.
Remote Work :
No
Employment Type :
Full-time
Provides Administrative support byassisting with routine quality assurance activitiesperforming administrative functions within the QA groupsupporting Quality-related Help Desk and e-mail requestsassisting in Analytical Subcontractor documentation maintenanceSupports Data Reporting by:reviewing appr...
Provides Administrative support by
- assisting with routine quality assurance activities
- performing administrative functions within the QA group
- supporting Quality-related Help Desk and e-mail requests
- assisting in Analytical Subcontractor documentation maintenance
Supports Data Reporting by:
- reviewing approving and releasing laboratory data
- assisting with review and approval of Certificates of Analysis and Cumulative Reports
- assisting with review and verification of Technical Reports and Summaries
Assists in Document Control by:
- issuing Master Lists numbers
- issuing Laboratory Notebooks and Logbooks
- issuing and maintaining Controlled Copies
- maintaining the Technical Library
- maintaining Archival of Records
Supports Stability activities as assigned
Supports Manufacturing activities as needed by:
- executing the quality assurance roles of batch records
- Other duties as assigned
Qualifications :
Required: a minimum of High School Diploma or Equivalent. Preferred Bachelors Degree and/or certifications in laboratory/quality/regulatory
Required: Understanding of FDA requirements and Quality Systems
Preferred: Must have good administrative skills (Microsoft Office Suite LIMS QMS)
Preferred: 1 2 Years in a laboratory environment.
Preferred: 3 years of GLP/GMP environment in laboratory operations or QA or combination of both
Additional Information :
Position is full-time Monday - Friday 8:00am - 5:00pm . Candidates currently living within a commutable distance of Cary NC are encouraged to apply.
- Excellent full time benefits including comprehensive medical coverage dental and vision options
- Life and disability insurance
- 401(k) with company match
- Paid vacation and holidays
Eurofins USA BioPharma Services is a Disabled and Veteran Equal Employment Opportunity employer.
Remote Work :
No
Employment Type :
Full-time
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