Senior Validation Specialist for Pharmaceutical Industries
23 hours ago
Accelerate Your Career in the Pharmaceutical Industry
Vti Inc. is seeking a Senior Cleaning Validation Engineer/Specialist to support our teams of industry subject matter experts and thought leaders.
This project will be based in London, Ontario, Canada and is expected to last for approximately 3+ months.
Responsibilities:
- Develop and implement cleaning validation protocols in a cGMP facility.
- Maintain all documentation related to cleaning cycle development and validation.
- Participate in cleaning cycle development activities including parameter selection, determining order of operations, authoring development and validation protocols, and reports.
Qualifications:
- 5+ years of experience in Cleaning Validation 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.
- Demonstrated ability in reviewing/writing technical documents, risk assessment reports, validation documents, IOQ protocols, and final reports.
What We Offer:
- A competitive salary range of $80,000 - $110,000 per annum, depending on experience.
- Opportunities for professional development and training.
- Excellent benefits package.
- 401K plan.
- A stimulating and collaborative work environment that values trust, respect, openness, teamwork, creative talent, enthusiasm, and diligence.
About Vti Inc.
Vti Inc. strives to maintain and inspire professional excellence by providing Commissioning, Qualification, Quality Engineering, Automation, and Validation Services to the Pharmaceutical, Biotechnology, Biologics, and Medical Device industries.
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