Industrial Validation Professional
4 days ago
Cpl Healthcare, in partnership with our client Pfizer, are seeking an experienced Cleaning Validation Specialist to join their team for a fixed-term contract at their state-of-the-art facility.
The successful candidate will be responsible for supporting new product introduction and cleaning validation activities across the site. This role is critical to ensuring that cleaning validation programs are robust, audit-ready, and enable efficient operation of the plant.
This position offers an ideal development opportunity to work within a dynamic team providing cleaning validation support to manufacturing areas and contributing to process transfer and new product introduction projects. The Cleaning Validation Specialist will provide technical support for cleaning validation activities and strategies for equipment used in the manufacture of drug substances and drug products.
Key Responsibilities:
1. Providing technical support for cleaning validation execution, design, monitoring, and troubleshooting
2. Generating, reviewing, and approving documentation for cleaning validation, including protocols, summary reports, validation plans, and supporting documents
3. Cleaning validation execution, including cleaning monitoring
4. Developing and maintaining cleaning validation strategies, including product and equipment grouping strategies
5. Collaborating with multifunctional teams to deliver projects on time and driving continuous improvements within the group
Requirements:
• A minimum of 2 years cGMP industrial experience with good technical writing skills
• Minimum 12 months of Cleaning Validation experience
• Demonstrated aptitude for technical learning and problem-solving
• Continuous improvement mindset to drive positive change
• Proactive, persistent, and good communication skills
Education:
A third-level qualification in Science or Engineering is required.
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