Job Title: Process Validation Engineer
Location: Warsaw, IN
Rate: $52/hr on C2C
JD:
Develops and Executes Process Validation Strategies Creates plans, protocols (IQ, OQ, PQ), and risk assessments to ensure effective processes for medical devices and equipment. Ensures Regulatory Compliance Adheres to FDA (21 CFR 820), ISO 13485, and other relevant regulations, participating in audits and maintaining up-to-date knowledge.
Analyzes Data and Reports Findings Compiles and analyzes validation data, writes comprehensive reports, and identifies trends for process improvement. Collaborates Cross-Functionally Works with Manufacturing, Quality Assurance, Engineering, and other teams to implement cleaning strategies, resolve issues, and provide technical support. Leads continuous improvement initiatives, manages change controls, troubleshoots cleaning problems, and ensures proper documentation and training. Creating, maintaining, and improving controlled technical documents such as prints, procedures, bills of materials, and routers.
Conducting feasibility study to estimate a product cost and analyze capital equipment, capacity, and capability requirements establishing and improving process methods that meet performance and quality requirements
Developing and executing project plans and schedules for work activities Communicate (written and verbal) direction and project plans with appropriate personnel from other departments.
Thanks & Regards,
Bhargavi Jaltar
Lead Sr. US IT Recruiter
Galaxy i Technologies, Inc
Location: 9927 E Bell Road, Suite 110
Scottsdale, Arizona – 85260
Email Id: bhargavi1@galaxyitech.com