Process Validation Engineer
Process Validation Engineer
Posted on :
11-09-2025
Employer Active
1 Vacancy
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Job Description
Role & Responsibilities:
- 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.
- Analysis Data and Reports Findings Compiles and analyses 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.
- Supporting a wide variety of processing applications such as machining finishing forging casting cleaning heat treating bonding moulding etc.
- Conducting feasibility study to estimate a product cost and analysed 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.
- Evaluating multiple options to select the most appropriate processes and machining methods Execute equipment qualification or process validation project(s).
Employment Type
Full-time
Key Skills
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