Our client, a pharmaceutical manufacturing company, is seeking a Validation Engineer to support the introduction of new equipment. The role will involve full lifecycle validation responsibilities, working cross-functionally with technical, production, and quality teams.
Key Responsibilities:
* Lead the preparation, execution, coordination, reporting, and closure of validation deliverables, including:
* Equipment qualification (IQ/OQ/PQ)
* Cleaning validation
* Process validation
* Provide QA support during technology transfer, equipment qualification, and cleaning validation development
* Ensure compliance with internal procedures and validation master plan (VMP)
* Collaborate with cross-functional stakeholders including Technical, Production, and Quality teams
* Support risk assessments and quality documentation related to validation activities
Required Experience:
* Minimum 3 years’ experience in a validation-focused role within a GMP-regulated pharmaceutical or life sciences environment
Preferred Experience:
* Equipment qualification (IQ/OQ/PQ), particularly new equipment introduction
* Cleaning validation and process validation
* Familiarity with Quality Management Systems (QMS)
* Risk management methodologies
* Project management exposure
Key Skills & Competencies:
* Strong communication and problem-solving skills
* Excellent project coordination and cross-team collaboration
* High attention to detail
* Technical writing: protocols, reports, procedures, and recipes
* Effective issue resolution and decision-making
* Strong IT proficiency (validation and documentation systems)
Ideal Candidate Profile:
A hands-on, proactive professional who brings practical experience, self-motivation, and a strong sense of ownership. You should be confident engaging in validation activities from planning through to execution and reporting.
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