Validation Engineer
Validation Engineer
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1 Vacancy
Job Description
Responsibilities:
- Conceives plans and executes manufacturing process validations plans and studies.
- Adhere to the Change Control and Design Control requirements.
- To create robust validation documents such as Master Validation Plans / Report IQ OQ & PQs.
- Being the lead on the writing and of IQ/OQ/PQ protocols.
- RCH/PCH Routing in MAP Agile & follow up till release.
- Updating Control Plan (CP) Assembly Procedure (AP) & Traveler document (TD).
- Preparing protocol & executing Test Method validation (TMV).
- Validation experience using riskbased approach guidelines international regulatory requirements and standards.
- Ensure that all activities are carried out in compliance with all regulations and laws governing business and quality operations.
- Responsible for ensuring compliance with all local national international and company regulations policies and procedures for Health Safety and Environmental compliance.
Requirements:
- Degree qualified ideally science or engineering.
- Other further education and work experience may be considered.
- Minimum 3years experience of working on manufacturing engineering validation activities.
- Some previous experience in medical device or related regulated industry.
- Experience in project management and project leadership.
- Extensive experience in the preparation of technical documents.
- Excellent written and oral communication skills.
- Ability to work as a team.
- Manage your own time and workload
- Excellent organizational skills.
Employment Type
Full Time
