Engineering - IE_Commissioning Engineer - Cleaning Validation

Job Description Tittle: Commissioning Engineer - Cleaning Validation Location: Dublin, Ireland Contract Duration: 12-month contract Rate: 442.00 Daily Looking to advance your career in cleaning validation? Join a major sterile drug product facility project and play a key role in delivering cleaning validation activities within a cutting-edge GMP biopharmaceutical manufacturing environment. Key Responsibilities Develop and implement cleaning validation strategies for new equipment and manufacturing processes. Execute cleaning validation studies, including sampling, testing, data analysis, and reporting. Perform risk assessments to identify critical cleaning parameters and acceptance criteria. Lead and support cleaning validation activities for new product introductions and process performance qualification (PPQ). Collaborate with Manufacturing, Quality, Engineering, and Validation teams to coordinate validation activities. Support investigation activities, deviation management, and troubleshooting using Quality Management Systems (QMS). Generate cleaning validation documentation, including protocols, reports, and release memos. Support Lockout/Tagout (LOTO) activities and develop standardized Energy Control Plans (ECPs). Oversee visual inspection qualification and requalification programs. Ensure compliance with site procedures, cGMP requirements, and global regulatory guidelines. Requirements Bachelor's or Master's degree in Engineering, Science, or a related discipline. 3-5 years' experience in a similar Cleaning Validation role within a pharmaceutical, healthcare, or GMP-regulated laboratory environment Strong understanding of cleaning validation principles and regulatory expectations (FDA, EMA, ICH, PDA). Experience supporting validation, commissioning, qualification, or manufacturing operations. Excellent problem-solving, communication, and cross-functional collaboration skills. Ability to work independently and manage multiple priorities in a fast-paced project environment. Previous cleaning validation experience within pharmaceutical or biopharmaceutical manufacturing. Knowledge of biopharmaceutical manufacturing processes and validation activities. Experience supporting sterile drug product or aseptic filling operations. Familiarity with deviation investigations, CAPA management, and QMS systems. We're actively shortlisting, apply now or get in touch today to avoid missing out!!