A global healthcare leader is seeking a Quality Engineer | Validation professional to join their team. This is an initial 6-month contract.
Key Responsibilities:
* Review and approve all validation deliverables for equipment, facilities, utilities, software, spreadsheets, and analytical validations at the site.
* Develop and maintain Quality System procedures.
* Ensure the site delivers safe and effective products that meet customer needs while maintaining compliance.
* Monitor and maintain the quality and compliance status of associated quality records.
* Maintain the quality and compliance status of associated Procedures, work instructions, and training materials.
* Present and communicate status, report metrics, identify trends, potential issues, improvement initiatives as applicable.
* Participate in continuous improvement programs to implement improvements in manufacturing, quality, safety, and training systems.
Ideal Background:
Relevant third-level qualification, Engineering/Manufacturing/Science preferred. Minimum 2 years in Engineering/Manufacturing/Scientific. Must have a minimum of 1-2 years validation experience within the areas of manufacturing or Testing Laboratories with emphasis on software and equipment validations.
A self-starter who can prioritize own work. Experience of Manufacturing Execution Systems desirable. Experience of manufacturing Database desirable.