Specialist QA II Manufacturing Oversight

Specialist QA II Manufacturing Oversight 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. Position Summary The QA Specialist II – Manufacturing Oversight will perform manufacturing oversight activities to ensure compliance with policies and procedures. Oversight activities include, but are not limited to, real‑time manufacturing batch record review, review of manufacturing documentation (logs, charts, etc.), and resolution of issues on the manufacturing floor. Essential Functions & Responsibilities Understand processes such as Quality Systems (e.g., Deviations, Corrective and Preventive Action reports (CAPAs), Change Controls, and Out of Specifications (OOSs)). Perform Quality Assurance review and approval of Deviation Reports. Understand cGMP and regulatory compliance as defined in government regulations such as 21 CFR Parts 11, 210, 211, and 600. Perform oversight and inspections of active production areas to resolve problems and ensure compliance with SOPs and policies. Perform general oversight of Buildings 1 and 2 (including cold rooms/freezers) and their associated activities, as required. Review and release Plasma pools to manufacturing. Review all manufacturing support documentation (logbooks, log sheets, charts, etc.). Review and release raw materials in LIMS/SAP. Perform audits of Nitrogen receipt process. Perform notification and disposition of associated Lookback units. Assist with quarantining and release of critical systems, equipment, and controlled environments. Write, review, and revise QA SOPs. Review SOPs and documents from other departments and provide feedback as necessary. Work with other departments to assess if Deviations, CAPAs, and Change Controls are required. Assist with training of new employees. Coordinate and perform any additional activities or projects assigned by QA Management. Experience with LIMS and SAP preferred. Job Requirements Education Requirements: Bachelor’s Degree preferred but can be offset by experience. Experience Requirements: 3–5 years’ experience in the pharmaceutical or biotechnology industry or other related industry. Competencies Exceptional organizational and communication skills. Excellent writing and oral skills. Benefits 401(k) plan with employer match and immediate vesting. Medical, Vision, Life and Dental Insurance. Pet Insurance. Company paid STD and LTD. 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 ADMA Biologics is an Equal Opportunity Employer. #J-18808-Ljbffr BioSpace