We are currently seeking a Senior Cleaning Validation Engineer/Specialist for our client in London Ontario Canada. This project will start in January 2025 and is expected to last for approximately 3+ months.
Responsibilities:
- Post cleaning validation monitoring, cleaning cycle development and cleaning validation in a cGMP facility.
- Maintain all documentation pertaining to cleaning cycle development and validation.
- Participate in cleaning cycle development activities including parameter selection, determining order of operations, Author development and validation protocols, and reports.
- 5+ years of Cleaning Validation experience in Biotech/Biologics/Pharma industries.
- Bachelor's degree or higher in Engineering, Chemistry, Biology, Chemical Engineering, or related discipline.
- Hands-on experience supporting/executing IQ, OQ (IOQ) equipment qualification related to various cleaning processes and activities in a solid dose facility.
- Thorough knowledge of cGMP/FDA regulations and clean room environment.
- Demonstrated ability in reviewing/writing technical documents, risk assessment reports, validation documents, IOQ protocols and final reports.
- Strong interpersonal skills, attention to detail, excellent review and analytical skills.
- Must be able to organize and manage multiple tasks in a fast-paced environment
As one of the leading global Commissioning, Qualification and Validation Services organizations, VTI is always looking for innovative, talented and experienced validation professionals for our multinational and global offices. We offer some of the best salary and benefit packages in the industry for our full-time/permanent employees. www.validation.org
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