Senior Process Cleaning Validation Specialist

Inc. (Vti); London; On-site; CAD 80,000 - 120,000; Full time

Job summary

VTI Life Sciences is seeking a Senior Cleaning Validation Engineer in London, Ontario for a project starting January 2025, lasting approximately 3 months. The role involves cleaning cycle development and validation in a cGMP facility, requiring strong background in biopharma cleaning processes.

Benefits

Competitive compensation

Excellent benefits

401K plan

Professional development and training

Qualifications

• 5+ years of Cleaning Validation experience in Biotech / Biologics / Pharma industries.
• Hands-on experience with IQ, OQ, IOQ equipment qualification.
• Thorough knowledge of cGMP / FDA regulations.

Responsibilities

• Perform post cleaning validation monitoring in a cGMP facility.
• Develop and maintain documentation for cleaning cycle validation.
• Participate in the development of cleaning validation protocols and reports.

Skills

Attention to detail

Interpersonal skills

Analytical skills

Education

Bachelor’s degree in Engineering, Chemistry, Biology, or related discipline

Job description

VTI Life Sciences (VTI) is seeking forward-thinking and ambitious engineers looking to accelerate their career in the pharmaceutical, biotechnology, and medical device industries. We offer an opportunity to help support our teams of industry subject matter experts and thought leaders while consulting with some of the biggest companies in the Life Sciences industries.

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, authoring development and validation protocols, and reports.

Qualifications :

• 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.

VTI Life Sciences 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. VTI offers professional development, training, competitive compensation, excellent benefits, 401K, plus a stimulating and collaborative work environment. We are committed to providing exciting career opportunities in a work environment that values trust, respect, openness, teamwork, creative talent, enthusiasm, and diligence.

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.

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