Grifols is seeking a Quality Compliance Auditor with in-depth knowledge of cGMPs and demonstrated application of robust Quality Systems. The Quality Auditor is recognized as an authority in multiple areas and able to independently develop and implement solutions for a variety of quality related objectives and influence the direction of complex projects.
This position functions as a Quality Compliance internal auditor to assess and verify overall compliance of the Clayton Quality System with regulatory requirements and applicable company policies and procedures. This office-based position is routinely scheduled to work Monday through Friday for an 8-hour interval during dayshift at the Clayton, NC site. Work on other shifts or days may be required and/or assigned for specific periods by management, including the requirement to travel during non-dayshift hours for work-related projects/duties. Overtime may be required as needed.
Primary Responsibilities for the Role:
Plan, schedule, lead, and execute, or otherwise participate in routine and directed internal audits utilizing knowledge of US and foreign regulations, guidances, and industry standards for pharmaceutical and medical device manufacturing
Review and analyze data, prepare and review reports; follow-up on observations and/or verify corrective action activities from previous audits; collaborate with manufacturing and QA/QC on corrective and preventive actions (CAPAs) associated with internal or external audits or other sources, projects, incident investigations, and change controls, for improvement of Quality Systems, etc.
Support site regulatory and customer audits, perform audit follow-up activities by requesting responses, tracking corrective actions and implementation status.
May also lead/participate in supplier management external audits and other supplier quality activities; author, edit, and/or publish SOPs, BPRs, purchase specifications, and other documents as directed using company prescribed computer software and systems.
Performs routine surveillance of current regulatory changes and expectations and incorporates them into the working operations of the company.
May be responsible for training other employees and is a fully qualified professional who requires minimal supervision.
Perform other duties as assigned by Quality Compliance management.
Knowledge, Skills and Abilities:
Excellent communication skills (written and verbal) with basic knowledge/understanding of domestic (i.e. Food and Drug Administration) and applicable foreign regulatory agency requirements/guidelines
This position is routinely scheduled to work Monday through Friday for an 8-hour interval during dayshift. Work on other shifts or days may be required and/or assigned for specific periods by management, including the requirement to travel during non-dayshift hours for work-related projects/duties. Overtime may be required as needed.
BA/BS required preferably in a STEM (science, technology, engineering, or mathematics) curriculum
Experience: 5 - 8 years relevant experience
**Must possess current ASQ auditor certification: Certified Quality Auditor`(CQA), Certified Biomedical Auditor (CBA) or equivalent auditor certification from a recognized professional certification authority. Must possess adequate proficiency in the use of Word and Excel computer software.
Working knowledge of SAP functionality is desirable.
Internal Number: 132630
About Grifols Therapeutics
For more than 75 years, Grifols has worked to improve the health and well-being of people around the world. We are a global healthcare company that produces essential plasma-derived medicines for patients and provides hospitals and healthcare professionals with the tools, information and services they need to deliver expert medical care.