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CLEANING VALIDATION SPECIALIST
Job Purpose:
We are looking for a Cleaning Validation Specialist to support new product introduction and cleaning validation activities across the site.
The role focuses on cleaning validation execution, design, monitoring and troubleshooting, including leading and resolving technical issues and manufacturing investigations related to cleaning processes.
The specialist will support process transfer, new product introductions, facility design, and equipment design specifications.
Job Responsibilities:
This is a non-laboratory based role supporting the site cleaning validation program and equipment cleaning strategies.
Generate, review and approve documentation for cleaning validation including protocols, summary reports, validation plans and supporting documents.
Generate, review and approve validation deviations and ensure successful implementation of corrective actions.
Write impact assessments in support of investigation closures.
Provide expertise for troubleshooting and resolution of problems.
Co-operate with multifunctional teams to deliver projects on time.
Support bench-scale studies such as cleaning efficacy, recovery studies and solubility.
Develop and maintain cleaning validation strategies including product and equipment grouping strategies.
Develop and maintain cleaning acceptance criteria for manufacturing equipment.
Identify and drive continuous improvements within the group to ensure streamlined and efficient cleaning validation.
Technology transfer for new processes, process changes and new product introductions.
Regulatory inspection support and close-out of regulatory follow-up measures.
Skills:
Minimum of 2 years cGMP industrial experience in manufacturing process, process development or technology transfer with good technical writing skills.
Minimum of 6 months cleaning validation experience or strong technical knowledge of cleaning validation; other relevant experience may be considered.
Demonstrated aptitude for technical learning and problem solving.
Continuous improvement mindset to drive positive change.
Proactive, persistent, and good communication skills.
Education:
Third-level qualification in Science or Engineering is required.
Exceptions may be considered where relevant skills/experience and correct attitude and behaviours exist (additional education can be pursued in parallel).
Working Patterns and Duration:
Day based Monday to Friday.
Work location assignment: Hybrid.
Additional Information
In order to be considered for this position in Ireland you need to be legally eligible to work in Ireland.
Please note there is no relocation support available for this position.
How to apply
Make a difference today, all suitable candidates should apply with a CV below.
We are looking forward to hearing from you!
Equal Employment Opportunity
We believe that a diverse and inclusive workforce is crucial to building a successful business.
As an employer, Pfizer is committed to celebrating this, in all its forms – allowing us to be as diverse as the patients and communities we serve.
Together, we continue to build a culture that encourages, supports and empowers our employees.
Disability Inclusion
Our mission is unleashing the power of all our people and we are proud to be a disability inclusive employer, ensuring equal employment opportunities for all candidates.
We encourage you to put your best self forward with the knowledge and trust that we will make any reasonable adjustments to support your application and future career.
Your journey with Pfizer starts here!
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