Sr. Quality Associate II / Principal, QA -Computer Systems

GRIFOLS, S.A.•NC-Clayton, CA

9d•Onsite

About The Position

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.

Requirements

BS/BA, preferably in a STEM field.
Minimum 5 years relevant experience or equivalent education/experience/competency mix.
Minimum 6 years relevant experience or equivalent education/experience/competency mix.
Minimum 8 years relevant experience or equivalent education/experience/competency mix.

Nice To Haves

Extensive experience with SAP QM, particularly with inspection plans, master inspection characteristics, sampling procedures, reportable characteristics, and Engineering Change Management.

Responsibilities

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.
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.
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.
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.