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!!