Zimmer Biomet Work Values

Daily Duties at Zimmer Biomet:

Lead internal GMP Quality System audits to ensure compliance with FDA and EU cGMP regulations. Assist cross functional teams with third party and regulatory audits. Assist with audit responses for third party audit observations. Generate deviation reports and implement CAPA programs. Compile technical data and short summary data analysis reports. Direct and develop quality improvement plans and operational action plans which includes SOPs and work instructions to mitigate GMP issues.

What they like about Zimmer Biomet:

You highly value a work environment built on a formal structure, rules, and regulations. You do not enjoy the unpredictability of shifting priorities and deadlines that upset your routine. You require and enjoy direction, input and accountability as part of your work environment. You have a strong need to participate in making key decisions and feel left out if your superiors or co-workers do not seek your input when making decisions. You thrive on providing good customer service to both internal or external customers, and doing so makes you feel good.

Tags

North Carolina, South Carolina, Florida, Texas, Missouri, Chicago, Atlanta, Associate Director of Quality Assurance, Quality Assurance Manager, Sr. Compliance QA Manager, Associate Director of Validation, Validation Director, CAPA Management, Supplier QA Manager, Director of Supplier Assurance, CMO QA Manager, Pharmaceutical QA Manager, Medical Device QA Manager, Corporate QA Auditor, CAPA Manager, API Manufacturer, Sterile Fill Pharmaceutical Manufacturer, Medical Device Manufacturer, Sr. Quality Engineer, Oklahoma, Illinois, Milwaukee WI, Validation Manager, Internal QA Auditor

Skills

GMP CAPA assessments, GMP MFG Audits / Supplier Audits, Change Management, Process Change Controls, Process Optimization, Pharmaceutical and Medical Device Operations, Risk Management, Validation Management, Validation Master Plans, Validation Protocol Development, Risk Management, Project Management, Facility / Equipment Qualifications, Problem Solving, Deviation / CAPA Remediation, Team Leadership, Training Programs, Regulatory Compliance, Supplier Quality Management, Supplier Quality Agreements

These are some of the questions we asked our climbers about their experiences with Zimmer Biomet: