QA Specialist I - Document Control - Adma Biomanufacturing Llc

ADMA Biologics is a biopharmaceutical company relentlessly committed to creating superior products for immunodeficient patients at risk for infec...

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.