Quality Associate, QC

GRIFOLS, S.A.•Clayton, NC

45d•Onsite

About The Position

The Quality Associate, QC provides routine technical support for various tasks (i.e. documentation, training, compliance, test review, scheduling, etc.), assignments, projects, etc. for the QC Sterility laboratory. He/she will be responsible for coordinating work assignments or training a small shift or group of employees in the Sterility laboratory.

Requirements

BA/BS - preferably in a STEM (science, technology, engineering, or mathematics) curriculum and 2 yrs of relevant experience or an equivalent combination of education and experience.
Proficiency using SAP is strongly preferred.
Detail oriented and great organizational and communication skills are a must.
Excellent prioritization, multitasking and leadership skills are crucial.
Depending on the area of assignment, directly related experience or a combination of directly related education and experience and/or competencies may be considered in place of the stated requirements. Example: If a job level requires a bachelor’s degree plus 4 years of experience, an equivalency could include 8 years of experience, an associate’s degree with 6 years of experience, or a master’s degree with 2 years of experience.

Responsibilities

Collects, reviews, and analyzes data.
Makes decisions independently, but within a well-defined area.
Addresses and resolves problems according to written procedure (i.e. SOP, etc.) or practice.
Coordinates work activities and scheduling.
Coordinates employee training.
Communicates effectively and promptly at all levels of the organization, supporting department objectives and management decisions.
Contributes cross-functionally within the departmental hierarchy
Demonstrates high levels of value and integrity.
Follows cGMP and department safety practices.
Apply expertise in testing to develop, validate and troubleshoot analytical methods.
Serve as SME for laboratory assays and act as a resource for laboratory staff.
Perform investigations and write reports.
Author SOPs and other laboratory documents.
Collaborate with production and Quality Assurance and Compliance on projects, incident investigations, and annual product reviews.
Evaluate data and perform statistical analysis for various projects.
Serve as system administrator and SME for various laboratory information systems and applications as required.