QA Assistant

Union-Agener

Augusta (GA)

On-site

USD 42,000 - 56,000

Full time

6 days ago
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Benefits offered by this job

401(k) Plan + Company Match
Vacation + End of Year Vacation (公司赞助)
Growth Opportunities to expand your事业

Job summary

Union-Agener is seeking a detail-oriented QA professional to support documentation and quality control processes in a manufacturing environment in Augusta, GA. The role involves batch record handling, document control, training module maintenance, and archival duties, with SAP knowledge as a preferred asset.

The ideal candidate will have a high school diploma or GED (an associate's degree is preferred) and at least 3 years of QC/QA experience, along with familiarity with cGMP guidelines and

Qualifications

  • Minimum of a High School Diploma or GED.
  • Preferred Associate's degree in a technical related field.
  • Three (3) years of experience in Quality Control or Quality Assurance.
  • Demonstrated knowledge/application of cGMPs and other pharmaceutical guidelines.

Responsibilities

  • Print and issue batch records and labels for all manufacturing operations.
  • Execute Document Requests to Create, Revise, Cancel, or Print.
  • Act as a documentation steward (ensures a coordinated review of all associated documents).
  • Perform document release (ensures a coordinated release of all associated documents).
  • Perform document distribution (controlled copy), communication (email), and archive.
  • Act as archive room manager.
  • Support Training Module Management (courseware requests, roster inquiries, processing course credits, test answer keys).
  • Maintain training modules and SOPs related to documentation activities.
  • Spreadsheet and database maintenance.

Skills

Detail oriented
Results oriented
Strong interpersonal skills
Team oriented
Adaptability to change

Education

High School Diploma or GED
Associate's degree in a technical related field

Tools

SAP

Job description

Position Description, Functions, Duties and Tasks:
  • Print and issue batch records and labels for all manufacturing operations
  • Execute Document Requests to Create, Revise, Cancel, or Print
  • Act as a documentation steward (ensures a coordinated review of all associated documents)
  • Perform document release (ensures a coordinated release of all associated documents)
  • Perform document distribution (controlled copy), communication (email), and archive
  • Act as archive room manager
  • Support Training Module Management (i.e. courseware request, roster audience inquiries, processing course credits, test answer keys (SOP or module))
  • Maintain training modules and SOPs related to documentation activities
  • Spreadsheet and database maintenance
Minimum Qualification (Education, Experience and/or Training, Required Certifications):
Education:
  • Minimum of a High School Diploma or GED
  • Preferred Associate's degree in a technical related field
Experience:
  • Three (3) years of experience in Quality Control or Quality Assurance
  • Demonstrated knowledge/application of cGMPs and other pharmaceutical guidelines
Additional Preferences:
Required Skills:
  • Detail oriented
  • Results oriented
  • Strong interpersonal skills
  • Ability to work effectively with respect for others in a team environment
  • Adapt readily to change and have the desire to experience new challenges and opportunities
Preferred Skills:
  • Knowledge of SAP
  • Adapt readily to change and have the desire to experience new challenges and opportunities
Physical Demand Requirements:
  • Those associated with sedentary work
  • Must be able to climb stairs and ladders when required
  • Must be able to perform and review work in a manufacturing plant environment
What do we offer?
  • Competitive Benefits Package and Employee Assistance Program
  • 401(k) Plan + Company Match
  • Vacation + End of Year Vacation (Company Sponsored)
  • Growth Opportunities to expand your career
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