Job Description
Pharmaceutical company seeks experienced validation specialist with expertise in equipment validation, cleaning validation, and process operations for a role involving technical report writing and compliance with regulatory guidelines. We are currently recruiting for a highly skilled validation specialist to join our team at a leading pharmaceutical organization based in Cork. This is an excellent opportunity for a professional with a strong background in validation and compliance to make a significant contribution to the success of our company. **Key Responsibilities:** • Execute equipment development, cleaning validation, and performance qualification • Develop and implement validation strategies, coordinating with outside vendors and writing protocols independently • Analyze test results and prepare technical reports • Execute routine business activities, including equipment periodic reviews, cleaning periodic reviews, and CAPAs • Provide support during commissioning phases by reviewing and approving documents • Ensure documentation complies with regulatory standards • Participate in cross-functional problem-solving teams for troubleshooting and investigations • Provide technical input and support during regulatory inspections • Ensure adherence to regulatory guidelines and company policies **Requirements:** • B.Sc. degree in Chemical Engineering, Biochemistry, Microbiology, Chemistry, or a related field • Experience as a validation specialist in a pharmaceutical or highly regulated environment • Strong knowledge of GxP systems, including GLIMS and eVAL • Excellent communication and writing skills By joining our team, you will have the opportunity to work on complex projects, develop your expertise, and contribute to the success of our company. If you are a motivated and experienced professional looking for a new challenge, we encourage you to consider this opportunity.