QA Specialist I - Document Control - Adma Biomanufacturing Llc
Boca Raton, FL 33487
About the Job
Create, format, revise, and proofread controlled documents, including Standard Operating Procedures (SOPs), Forms, Validations, etc., from various departments such as Quality Assurance, Manufacturing, Facilities, and Quality Control.
Enforce access restrictions for secured controlled documents in both electronic and physical locations.
Process documents for approval, official distribution, and archiving.
Assist in maintaining on-site documentation inventory.
Support the maintenance of document retention and destruction schedules.
Perform general office duties such as photocopying, word processing, filing, scanning, maintaining physical inventory, and ordering supplies.
Ensure compliance with current Good Manufacturing Practices (cGMPs).
Proficiency in computer systems, including validation processes, role assignments, and training management.
Demonstrate a willingness to take on new projects as needed.
Education Requirements:
High school diploma required.
Experience Requirements:
Minimum of one year of experience in the pharmaceutical or biotechnology industry, with a focus on document management systems and software.
Benefits: 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)
Convenient access to Tri-Rail
Free shuttle service 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.
