Quality Systems Associate

GRIFOLS, S.A.•Huntington Beach, CA

4d•Onsite

About The Position

Under the direct supervision of the Quality Systems Manager, perform quality assurance and Training functions to ensure compliance with internal and external regulations and protocol. This role is responsible for completing weekly reviews of equipment QC and maintenance records, documenting, investigating, and performing root-cause analysis for deviations and customer complaints, specifically in how they related to product quality and/or donor safety. The associate will also inspect and release incoming supplies, investigate and report supplies that have not met quality specifications and requirements prior to use, and perform documentation review for unsuitable test results. Additionally, the associate will assist the Quality Systems Manager to ensure that cGMP regulation, SOPs and regulatory requirements are followed, including performing all product release activities, reviewing lookback information and documentation, waste shipment documentation, unexpected plasmapheresis events, electronic donor chart exceptions impacting donor eligibility/safety and/or product quality, donor deferral notifications from competitor centers, and plasma processing documentation to ensure proper freezing, storage, and handling of product. The role also involves assisting the Quality Systems Manager to ensure center training programs follow procedural requirements, which includes creating, maintaining, and auditing training records and files, performing employee training observations to ensure staff competency, and conducting required training activities for Center Notifications, Corporate Directives, SOP changes, and initial SOP implementations. On an occasional basis, when the Quality Systems Manager is absent, the Quality Systems Associate may be required to review and approve deferred donor reinstatement activities and assist with the completion of the internal donor center audit. The associate will also perform review of monthly trending reports, donor adverse events reports and applicable related documentation, and conduct training to address donor center corrective and preventative measures. This job description is intended to present the general content and requirements for the performance of this job and is not to be construed as an exhaustive statement of duties, responsibilities, or requirements. Managers and supervisors may assign other duties as needed.

Requirements

Developing command of interpersonal communication, organizational and problem-solving skills.
Ability to understand FDA regulations.
Strong integrity and commitment to quality and compliance.
Good knowledge of mathematics.
Legible handwriting.
Proficiency with computers.
Ability to work flexible scheduling to meet business needs.
Performs basic document review and employee observations.
Communicates openly with the CQM on issues noted during reviews.
Ability to understand and follow SOP’s and protocols.
Ability to perform primary responsibilities of the Quality Associate role in a proficient manner.
Has a basic understanding of cGMP and quality systems.
Is able to spend hours sitting and reviewing documentation for accuracy.
Demonstrates good organizational skills and attention to detail.
Is certified and maintains certification as a Donor Center Technician.

Nice To Haves

Ability to understand and follow SOP’s and protocols.
Ability to perform primary responsibilities of the Quality Associate role in a proficient manner.
Has a basic understanding of cGMP and quality systems.
Is able to spend hours sitting and reviewing documentation for accuracy.
Demonstrates good organizational skills and attention to detail.

Responsibilities

Completes weekly review of equipment QC and maintenance records.
Documents, investigates, and performs root-cause analysis for deviations and customer complaints, specifically in how they related to product quality and/or donor safety.
Inspects and releases incoming supplies. Investigates and reports supplies have not met quality specifications and requirements prior to use.
Performs documentation review for unsuitable test results.
Assists the Quality Systems Manager to ensure that cGMP regulation, SOPs and regulatory requirements are followed.
Performs all product release activities.
Reviews lookback information and documentation.
Reviews waste shipment documentation.
Reviews unexpected plasmapheresis events including electronic donor chart and related documentation pertaining to exceptions occurring during the donation process.
Reviews electronic donor chart exceptions impacting donor eligibility/safety and/or product quality.
Reviews donor deferral notifications from competitor centers.
Reviews plasma processing documentation to ensure the proper freezing, storage and handling of product.
Creates, maintains, and audits training records and files to ensure compliance.
Performs employee training observations to ensure staff competency prior to releasing employees to work independently.
Conducts required training activities for Center Notifications, Corporate Directives, SOP changes, and initial SOP implementations.
Reviews and approves of deferred donor reinstatement activities (when Quality Systems Manager is absent).
Assists with completion of the internal donor center audit (when Quality Systems Manager is absent).
Performs review of monthly trending report.
Performs review of donor adverse events reports and the applicable related documentation.
Conducts training to address donor center corrective and preventative measures.