QA Assistant

Union Agener; Augusta (GA); On-site; USD 45,000 - 65,000; Full time

Benefits offered by this job

Competitive Benefits Package

Employee Assistance Program

401(k) Plan + Company Match

Vacation + End of Year Vacation

Growth Opportunities

Job summary

Union Agener in Augusta, GA is seeking a detail-oriented Quality Control/Quality Assurance professional to support manufacturing documentation and archival processes. You will print and issue batch records, manage document requests, act as documentation steward, perform document release and distribution, and maintain training modules related to SOPs and documentation activities.

A background in cGMPs and manufacturing plant operations is preferred.

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

Teamwork

Adapt to change

Education

High School Diploma or GED

Associate's degree (preferred)

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