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The Validation Engineer has a significant impact to the company. There is a high criticality level for the work produced. The Validation Engineer is responsible for all aspects of the validation process, including: documenting commissioning activities,  establishing the process and equipment acceptance criteria, and developing and performing qualification studies to document evidence which provides a high degree of assurance that equipment and processes (including cleaning processes) will consistently produce a product meeting its predetermined specifications and quality attributes.
 
We’re looking for multiple Project Managers to join a closely-knit team in order to provide project leadership across various capacities within biopharma manufacturing. Current client sites are in NC, OH, NJ and MI.
 
This is a unique chance to be part of a globally successful consulting company and play a major role in facilitating a new & exciting US endeavor… a fantastic chance to gain experience across a breadth of project leadership.
 
To clarify, these are permanent positions with our client. The roles will be consulting on long-term projects… no travel requirements (no bouncing around to various client sites).
 
Our client was founded in Denmark in 2006 and established a US HQ in Raleigh, NC in 2015. Their sole focus is within the Life Sciences industries. Services provided are improvement programs, management consulting, project management, R&D support, supply chain planning and training for leading companies worldwide.
 
We’re looking for candidates with a natural curiosity, who are tech-savvy and have strong academic credentials & a ‘thinking outside the box’ mentality.
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