QA Specialist I - Document Control

Company: ADMA BIOMANUFACTURING LLC
Location: Boca Raton
Posted on: June 25, 2022

Job Description:

Job DetailsJob LocationADMA Biologics - Boca Raton, FLJob CategoryQA - Quality ControlDescriptionADMA 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. The QA 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.QualificationsCreate, 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 documentationAssist with the maintenance of document retention and destruction schedules.Perform general office duties such as photocopying, word processing, filing, scanning, physical inventory, ordering supplies, etcProficient in cGMPs.Proficiency in computer systems requirements, validations, role and training assignments. Willingness to take on new projects Education Requirements: High School diploma required. Bachelor's Degree preferred but can be offset by work experience. Experience Requirements: 1-2 years experience with in 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 vestingMedical, Vision, Life and Dental InsurancePet Insurance Company paid Short and Long-Term Disability PlansCompany Paid Holidays 3 Weeks' Paid Time Off (within the first year)Tuition Assistance (after the first year)Easily accessible to Tri-RailFree shuttle to the Boca Tri-Rail stationADMA 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.

Keywords: ADMA BIOMANUFACTURING LLC, Boca Raton , QA Specialist I - Document Control, Other , Boca Raton, Florida