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Sr. Quality Associate II/Principal, QA -Computer Systems
Job in
Clayton, Granville County, North Carolina, 27527, USA
Listed on 2026-07-15
Listing for:
Grifols SA
Full Time
position Listed on 2026-07-15
Job specializations:
-
Quality Assurance - QA/QC
Data Analyst, Quality Control - QC Analysts/Managers, Regulatory Compliance Specialist, QA Specialist - Analyst/Manager
Job Description & How to Apply Below
Location: Clayton
Would you like to join an international team working to improve the future of healthcare? Do you want to enhance the lives of millions of people? Grifols is a global healthcare company that since 1909 has been working to improve the health and well-being of people around the world. We are leaders in plasma-derived medicines and transfusion medicine and develop, produce and market innovative medicines, solutions and services in more than 110 countries and regions.
Schedule:
Day Shift
Sr. Quality Associate I / II / Principal, Quality Assurance:
Summary:
We are seeking an experienced Quality Assurance professional to join the General Computer Systems Group, supporting key initiatives such as the Laboratory Execution System (LES) project and SAP Quality Master Data management. This role is offered at three levels-Sr. Quality Associate I, Sr. Quality Associate II, and Principal Quality Associate-depending on experience and qualifications.
The ideal candidate brings extensive experience with SAP QM, particularly with inspection plans, master inspection characteristics, sampling procedures, reportable characteristics, and Engineering Change Management. You will be a technical expert who provides guidance across functions and may lead teams or projects of varying scope.
You will support and troubleshoot SAP-related issues across QA, QC, Planning, Manufacturing, and Finance; drive continuous improvement; and serve as a subject matter authority for multiple business areas.
Key Responsibilities:
Sr. Quality Associate I:
* Partner with management to develop and implement solutions to meet quality objectives.
* Use subject‑matter expertise to make independent decisions within defined areas.
* Participate on cross‑functional project teams.
* Collect, analyze, and interpret data.
* Demonstrate sound decision‑making with moderate guidance.
* Uphold cGMP and safety practices; model company values and integrity.
* Perform additional duties as assigned.
Sr. Quality Associate II:
* Advise and influence technical decisions within business units.
* Collaborate with management and, when necessary, regulatory officials.
* Lead cross‑functional teams and communicate proposals to senior management through successful project completion.
* Mentor team members as needed.
* Prepare, review, and/or approve SOPs, change controls, incident entries, and investigation reports.
* Make strong, independent quality decisions with minimal guidance.
* Perform additional duties as assigned.
Additional responsibilities may include advanced work in quality systems depending on business unit assignment.
Principal Quality Associate:
* Act as a technical authority influencing quality and business direction.
* Lead high‑impact, multi‑disciplinary project teams from proposal to completion.
* Maintain and advance essential technologies.
* Interact regularly with management and regulatory officials.
* Prepare, review, and/or approve SOPs, change controls, investigations, and regulatory documents.
* Easily prioritize and adapt to changing business needs.
* Provide SAP validation review and approval.
* Make fully independent quality decisions and influence stakeholders across departments.
* Perform additional duties as assigned.
Position‑specific responsibilities may include:
* Acting as author, reviewer, approver, administrator, or coordinator for quality systems.
* Supporting SAP QM (inspection lots, quarantine, batch release, production order issues).
* Providing SAP inspection plan support for Annual Product Reviews.
* Supplying Quality input for validations, clinical studies, stability programs, and regulatory submissions.
* Representing the Quality Manager in meetings and project forums.
* Communicating effectively across all levels of the organization.
Requirements:
Sr. Quality Associate I
* BS/BA, preferably in a STEM field.
* Minimum 5 years relevant experience or equivalent education/experience/competency mix.
Sr. Quality Associate II
* BS/BA, preferably in a STEM field.
* Minimum 6 years relevant experience or equivalent education/experience/competency mix.
Principal Quality Associate
* BS/BA, preferably in a STEM field (required).
* Minimum 8 years relevant experience or…
Position Requirements
10+ Years
work experience
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