Process Validation Engineer - Pharmaceuticals - Dublin - 12-Months Contract
Are you a Process Validation Engineer and wanting to join an international team working to improve the future of healthcare? Do you want to enhance the lives of millions of people? QCS Staffing’s client is a global healthcare company specialising in delivering lifesaving medicines globally. Our client has been at the forefront of delivering the health and well-being of people for the past 100 years, and now looking for a Process Validation Engineer to join their ever-growing team.
Key Responsibilities
* Write, review and execute Validation Protocols and Reports
* Generation and review of tech transfer documentation
* Development of site-based validation SOPS to latest regulations for CPV, VHP and SIP and autoclave validation
* Completion of risk assessments, closure of corrective and preventive actions
* Performs other validation associated activities as defined by Manager or Director
Key Experience
* Aseptic Process Validation Experience
* Tech Transfer project experience
* Strong understanding and experience with CQA's (Critical Quality Attributes), CPP's (Critical process parameters), CCS (contamination control strategy) and CPV (continued process verification).
* Good knowledge of Autoclaves and SIP's.
* Experience writing SOP’s
* Good communication skills and work ethic
If you are interested, please apply now for immediate consideration and further information.
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