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Validation and Quality Assurance Consultant - Hamlyn Williams
We are currently supporting a global biopharmaceutical organisation in their search for a Cleaning Validation Technical Specialist to join their team at a state-of-the-art bulk drug substance manufacturing facility in Dublin.
This is a high-impact role within a growing facility, offering the opportunity to lead cleaning validation activities across upstream and downstream operations, collaborate cross-functionally, and contribute to regulatory inspection readiness.
Key Responsibilities:
* Prepare and review cleaning validation documentation including protocols, reports, risk assessments, and impact assessments
* Lead cleaning verification efforts related to both commercial and new product introduction (NPI) activities
* Troubleshoot cleaning challenges and drive continuous improvement initiatives using Lean tools
* Support technical services and QA teams during regulatory inspections
* Assist with deviation investigations and manage change controls via eQMS
* Contribute to process optimisation and cross-functional technical projects
Key Requirements:
* Minimum of 2 years’ experience in cleaning validation, ideally in bulk drug substance or biopharma manufacturing
* Strong knowledge of cGMP, quality systems, and regulatory expectations
* Familiarity with upstream/downstream equipment and cleaning strategies in multiproduct facilities
* Proficiency in technical writing and use of digital tools (MS Office, Adobe, eQMS systems)
This is an excellent opportunity for a detail-oriented validation professional looking to work at the forefront of biopharma manufacturing and contribute to high-priority commercial and technical activities.
To apply or learn more, please submit your CV or reach out directly for a confidential discussion.
Seniority level
* Seniority level
Mid-Senior level
Employment type
* Employment type
Contract
Job function
* Industries
Pharmaceutical Manufacturing and Biotechnology Research
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