Senior Quality Analyst
About The Position
The Senior Quality Specialist is responsible for conducting quality-related activities to deliver consistent high-quality documents, services, products, and processes. The Specialist will maintain Quality Management Systems (QMS) for the activities within their scope, as well as for effective and lean QMS operating processes, adhering to FDA QMSR and IS 13486 regulations. ESSENTIAL FUNCTIONS: To perform this job successfully, an individual must be able to perform each of the following essential functions satisfactorily. Lead change order and change management efforts (document controls) for the company, including manufacturing transfer of documents. Experience with writing standard operating procedures (SOP) Conduct internal ISO audits and inspections to ensure compliance with quality and regulatory standards. Compile evidence and generate report of findings to share with Lead Auditor. Perform acceptance testing (final QC) on all completed refurbished systems (SPECT / SPECTCT / PET / PETCT) Collaborate with cross-functional teams to integrate quality into all phases of the warehouse operations. Participate in lean improvement projects for problem solving and process optimization. Maintain comprehensive records of inspections, and tests to contribute to the Device Medical Files. Facilitate work installation updates with subject matter experts to ensure documentation describes processes while being compliant with all related requirements. Update records and maintain all necessary documentation and certificates. Responsible for following management of change as process and procedures are updated as per QMS requirements. Perform regular process audits in Manufacturing areas and functional areas, including technical work instructions, processes, procedures, competence and ensure compliance. Other duties as assigned.
Requirements
- Associate Degree or relevant military experience
- 5+ years of experience in Quality Assurance or Control with ISO 13856 and FDA QMSR knowledge
- Proficiency with Microsoft Office Suite
Nice To Haves
- Bachelor’s Degree
- Experience in document control or change analysis
Responsibilities
- Lead change order and change management efforts (document controls) for the company, including manufacturing transfer of documents.
- Experience with writing standard operating procedures (SOP)
- Conduct internal ISO audits and inspections to ensure compliance with quality and regulatory standards.
- Compile evidence and generate report of findings to share with Lead Auditor.
- Perform acceptance testing (final QC) on all completed refurbished systems (SPECT / SPECTCT / PET / PETCT)
- Collaborate with cross-functional teams to integrate quality into all phases of the warehouse operations.
- Participate in lean improvement projects for problem solving and process optimization.
- Maintain comprehensive records of inspections, and tests to contribute to the Device Medical Files.
- Facilitate work installation updates with subject matter experts to ensure documentation describes processes while being compliant with all related requirements.
- Update records and maintain all necessary documentation and certificates.
- Responsible for following management of change as process and procedures are updated as per QMS requirements.
- Perform regular process audits in Manufacturing areas and functional areas, including technical work instructions, processes, procedures, competence and ensure compliance.
- Other duties as assigned.
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
Education Level
Associate degree
