About
An experienced Senior Validation Engineer is required to lead validation activities for cleanroom environments, purified water systems, and tablet press equipment within a regulated pharmaceutical manufacturing environment. The role involves ensuring compliance with GMP standards and driving continuous improvement across processes and equipment.
Increase your chances of an interview by reading the following overview of this role before making an application.
Key Responsibilities
- Develop and execute validation protocols (IQ, OQ, PQ) for facilities, systems, and equipment.
- Lead validation activities for cleanrooms, purified water systems, and tablet press equipment.
- Perform risk assessments and ensure compliance with industry regulations.
- Troubleshoot validation issues and provide technical support during audits.
- Maintain accurate documentation in line with GMP standards.
Education
- Bachelor’s degree in Engineering, Science, or related field.
- Minimum 5 years’ experience in validation engineering within a GMP-regulated environment.
- Proven expertise in cleanroom, purified water systems, and tablet press validation.
- Strong knowledge of GMP and regulatory requirements.
- Excellent problem-solving and communication skills. xcfaprz
- Attention to detail with a proactive approach to challenges.
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Languages
- English
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