Validation Specialist

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 Validation Engineer/Specialist for our client in London Ontario Canada. This project will be starting soon and is expected to last for approximately 2 months.

Responsibilities:

1. Write C/Q/V documents following established standards and templates, including but not limited to the following: WIFI and Clean Steam SOPs and Performance Qualification Protocols and Summary Reports.

Qualifications and Requirements:

1. Bachelor of Science in Engineering.
2. 2+ years of relevant experience.
3. Experience in Pharmaceutical, Biotech, Medical Device Design, Construction, Commissioning, Validation, or QA.
4. Proficiency with Microsoft Office Suite.

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. www.validation.org