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Job Responsibilities: Commissioning and Qualification of critical utilities including: DI Water Compressed Air Nitrogen HVAC Commissioning and Qualification of equipment and qualification of laboratory equipment Commissioning and Qualification documentation generation, review... ireland.xpatjobs.com – Posted by: xpatjobs.com |
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RESPONSIBILITIES: Complete validation plans, FMEAs, validation protocols, validation reports, control plans and test method validations supported with appropriate statistical tools in accordance with quality system and the requirements of ISO13485, The Medical Device Directive... ireland.xpatjobs.com – Posted by: xpatjobs.com |
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RESPONSIBILITIES: ? FDA validation requirements understanding ? Equipment, facilities CSV ? Development of IQ/OQ and PQ protocols ? Performance of qualification activities ? Validation report writing including Validation Master plans ? Risk Assessment ? SOP/specification... ireland.xpatjobs.com – Posted by: xpatjobs.com |
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My client is a leader within Generic companies. It covers the whole globe, aiming towards innovation and empowerment. The company invests in the employees, making sure each potential is discovered and developed. The business can offer career progression, a competitive salary... ireland.xpatjobs.com – Posted by: xpatjobs.com |
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My client is one of the most well known businesses within generic companies. It is a global corporation that has strong targets and impacts the society on a large scale. The culture in the company is motivational, developing each employee on a personal and professional level.... ireland.xpatjobs.com – Posted by: xpatjobs.com |
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my client is leading the Health care market and has a strong philosophy behind every decision. It is a global company with over 20,000 employees across the world. It invests money and time into developing the employees; there is always space to grow and progress. The business... ireland.xpatjobs.com – Posted by: xpatjobs.com |
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The key responsibilities of the role include maintaining assigned areas to the requirements of ISO 13485 and the FDA 21 CFR Part 820, as well as maintaining the compliance of the product to the Medical Device Directive. Areas of responsibility may include but are not limited... ireland.xpatjobs.com – Posted by: xpatjobs.com |
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Major Responsibilities: * Responsible for development an execution of plan to deliver process performance improvements related to Quality, Delivery, and Cost of a manufacturing process or line. * Develops change management plan and execution plan to improve flow of products,... ireland.xpatjobs.com – Posted by: xpatjobs.com |