QA Specialist I - Document Control
Location: Boca Raton
Posted on: June 23, 2025
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Job Description:
Job DetailsLevel EntryJob Location ADMA Biologics FL - Boca
Raton, FLPosition Type Full TimeEducation Level High SchoolTravel
Percentage NoneJob Shift DayJob Category QA - Quality
ControlDescription 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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