00 Validation Engineer
Job
ZimVie US Corp LLC
Riviera Beach, FL (In Person)
Full-Time
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Job Description
We are ZimVie, a global life sciences leader focused on restoring daily life by advancing clinical technology to improve patients' smiles, function, and confidence. Our company is founded on a legacy of trusted brands, products, and clinical evidence made possible through an inclusive and collaborative culture that empowers our team members to bring their whole selves
- their best selves
- to work every day to accomplish our Mission.
- -GxP regulations & state-of-the-art validation techniques used to ensure systems, processes, and equipment that impact product quality and patient safety are consistently compliant and reliable.
- Development, Implementation, and execution of Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ) system protocols for any system that creates, modifies, maintains, or transmits electronic records/data used in manufacturing, quality control, or documentation.
- Process, equipment and software validation for critical manufacturing processes, automated equipment, and quality-impacting software to prove they consistently meet predetermined specifications including but not limited to equipment such as CNCs, laser markers, packagers, vision systems, ultrasonic cleaning lines, mills, grinders, etc.
- Manufacturing practices including ISO 13485 and 21CFR820 guidelines used to establish, maintain, and ensure the compliance of the Quality Management System (QMS) for devices sold globally and in the U.S.
- Utilizing Statistical Process Control (SPC) Tools (e.g., Minitab) used to analyze validation data (especially for Process Performance Qualification, PPQ runs) to demonstrate process capability (Cpk) and statistical justification for acceptance criteria.
- Utilizing Risk Management Methodology (e.g., ISO 14971) used to formally assess and document risks associated with processes and equipment, which then justifies the scope and rigor of the validation effort.
- Utilizing Qualityze or Similar QMS Platform used to manage and document all controlled quality records, including Change Controls, Non-Conformances (NCs), and Corrective and Preventive Actions (CAPAs) that often stem from validation activities.
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