Grifols · 15 hours ago
Supervisor, Plasma Quality Assurance
North Carolina, United States
Full-time
Onsite
Senior Level
5+ years expGrifols is a global healthcare company that has been working to improve the health and well-being of people around the world since 1909. The QA Supervisor coordinates and supervises the inspection and release of plasma lots, ensuring compliance with approved procedures and overseeing the quality assurance staff's daily activities.
BiotechnologyHealth CareManufacturing
Responsibilities
Supervises the daily activities of the quality assurance staff and ensures that required activities related to the receipt, storage, clearing, processing of Lookback Alerts, quarantine of unsuitable units, and release of Source Plasma for further manufacture or sales
Responsible for the QA release of plasma from Plasma Logistic Center (PLC) and verifies that all shipment contents meet standard operating procedures, regulatory and customer requirements prior to release
Reviews and verifies temperature documentation to ensure conformance to appropriate temperature specifications
Investigates and documents deviations noted because of routine compliance reviews, internal and external audits and customer complaints
Participates in the writing and revision of policies and procedures related to Source Plasma at the facility
Monitors Plasma Operations to maintain compliance with all applicable regulations, cGMPs and CFRs. Participates in internal audit for the facility. Interfaces with multiple levels of management and various support and service groups internally and externally
Trains current and new employees maintains and updates training records of the QA staff. Supervises the activities of quality assurance staff including hiring, performance management, disciplinary action, and professional development
Meet quality assurance and company financial objectives by monitoring department costs
Qualification
Required
Bachelor's degree in life sciences or related field ideal
Typically requires a minimum of 5 years of Quality Assurance related experience and 3 years working in pharmaceuticals
Project or technical leadership experience required
Strong analytical, organizational and interpersonal skills with extensive knowledge of cGMPs as specified in the CFR/USP and EP Pharmacopeia / ICH and ISO Guidelines
Excellent written/verbal/leadership skills must be able to make sound decisions that may affect the quality purity or efficacy or a drug product
Ability to read and review documents for up to four (4) hours at a time
Ability to stand for extended periods of time - up to four (4) hours at a time
Ability to lift, tug, pull up to fifty (50) pounds
Ability to travel via automobile and/or airplane
Preferred
Supervisory or management experience preferred
Company
Grifols
Grifols is a global healthcare company.
10001+ employees
H1B Sponsorship
Grifols has a track record of offering H1B sponsorships. Please note that this does not
guarantee sponsorship for this specific role. Below presents additional info for your
reference. (Data Powered by US Department of Labor)
Distribution of Different Job Fields Receiving Sponsorship
Represents job field similar to this job
Trends of Total Sponsorships
2025 (2)
2023 (2)
2022 (1)
2020 (2)
Funding
Current Stage
Public CompanyTotal Funding
$2.51BKey Investors
Michael J. Fox Foundation
2025-01-14Grant· $21M
2024-06-04Post Ipo Debt· $1.41B
2024-04-23Post Ipo Debt· $1.07B
Leadership Team
Camille Alpi
Chief Human Resources Officer
Víctor Deu
Director of Planning & Control Department
Recent News
2025-12-24
Pharma Letter
2025-11-28
Company data provided by crunchbase