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QA Specialist I - Document Control

ADMA BIOMANUFACTURING LLC
Boca Raton, FL Other
POSTED ON 3/30/2025
AVAILABLE BEFORE 5/30/2025

Job Details

Level:    Entry
Job Location:    ADMA Biologics FL - Boca Raton, FL
Position Type:    Full Time
Education Level:    High School
Salary Range:    Undisclosed
Travel Percentage:    None
Job Shift:    Day
Job Category:    QA - Quality Control

Description

ADMA Biologics is a biopharmaceutical company relentlessly committed to creating superior products for immunodeficient patients at risk for infection. It is our devotion to this underserved population that fuels us and our hands-on approach to production and development that sets us apart.  If you are looking for a dynamic, innovative, growing company in the biopharmaceutical industry that is committed to excellence and integrity, then consider ADMA Biologics. We currently have an exciting opportunity available for a Quality Assurance Specialist I - Document Control in Boca Raton, FL!

 

The Quality Assurance Specialist I - Document Control will create, format, revise and proofread controlled documents such as Standard Operating Procedures (SOPs), Forms, Validations, etc. from departments including but not limited to Quality Assurance, Manufacturing, Facilities, and Quality Control. Perform general office duties such as photocopying, word processing, filing, scanning, physical inventory, ordering supplies.

Qualifications


  • Create, format, revise and proofread controlled documents such as Standard Operating Procedures (SOPs), Forms, Validations, etc. from departments including but not limited to Quality Assurance, Manufacturing, Facilities, and Quality Control.
  • Enforce limited access restrictions of secured controlled documents in the electronic and physical document locations.
  • Process documents for approval signatures, official distribution, and absolution.
  • Assist with maintaining inventory of on-site documentation.
  • Assist with the maintenance of document retention and destruction schedules.
  • Perform general office duties such as photocopying, word processing, filing, scanning, physical inventory, ordering supplies, etc.
  • Proficient in cGMPs.
  • Proficiency in computer systems requirements, validations, role and training assignments. 
  • Willingness to take on new projects.

 

Education Requirements:      

High School diploma required.  

 

Experience Requirements:    

Minimum of one year of experience in the pharmaceutical or biotechnology industry and document management systems and software.

 

In addition to competitive compensation, we offer a comprehensive benefits package including:

  • 401K plan with employer match and immediate vesting
  • Medical, Vision, Life and Dental Insurance
  • Pet Insurance 
  • Company paid Short and Long-Term Disability Plans
  • Company Paid Holidays 
  • 3 Weeks’ Paid Time Off (within the first year)
  • Tuition Assistance (after the first year)
  • Easily accessible to Tri-Rail
  • Free shuttle to the Boca Tri-Rail station

 

ADMA Biologics uses E-Verify to confirm the employment eligibility of all newly hired employees. To learn more about E-Verify, including your rights and responsibilities, please visit www.dhs.gov/E-Verify. 

 

ADMA Biologics is an Equal Opportunity Employer.

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