Senior Pharmaceutical Commissioning Validation Expert
1 day ago
We are seeking a seasoned CQV Engineer to join our team in Australia. The ideal candidate will have extensive experience in commissioning, qualification, and validation of pharmaceutical facilities.
Key Responsibilities:- Develop documentation for the Commissioning, Qualification, and Validation of pharmaceutical facilities, utilities, and equipment.
- Plan, coordinate, and direct small teams in document development and execution.
- Provide cGMP leadership and guidance for the integration and delivery of CQV services for life sciences clients.
The successful candidate will possess strong technical problem-solving skills, attention to detail, and excellent communication abilities.
Requirements:- Bachelor's or Master's degree in a relevant science or engineering field.
- 5-12 years of hands-on experience in commissioning and/or qualification activities in an FDA-regulated industry.
- Strong knowledge of typical project technical issues and ability to troubleshoot effectively.
- Competitive salary package.
- Opportunities for professional growth and development.
- A supportive and collaborative work environment.
We are a leading provider of commissioning, qualification, and validation services for life sciences companies. Our team is dedicated to delivering high-quality results and exceeding client expectations.
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