Syner-G
Biopharma
ValidationEngineer
Neural analysis suggests this role is
optimal for Mid+ candidates.
“Validation Engineer at Syner-G. Skills: Validation, Qualification, Documentation. Generate life cycle documentation. Execute life cycle documentation”
What You'll Achieve.
Drive overall quality performance; Maintain validation program
Industry & Context.
Root cause analysis
Lift up to 25 pounds, Close vision, Adjust focus
What They're Looking For.
Must Have
Validation Engineer experience, 5+ years experience
Nice to Have
Experience with Basecamp, Experience with client Tech Transfer projects
What You'll Do.
Generate life cycle documentation
Execute life cycle documentation
Support validation activities
Generate validation life cycle documents
Execute validation life cycle documents
Review validation life cycle documents
Close validation life cycle documents
Write qualification documents
Review qualification documents
Revise qualification documents
Write verification documents
Review verification documents
Revise verification documents
Write validation master plans
Write execution plans
Write automation documents
Write engineering design documents
Write commissioning documents
Write qualification documents
Write technical documents
Write user requirement specifications
Write functional requirement specifications
Write detailed design specifications
Write factory acceptance test documents
Write verification protocols
Write commissioning test procedures
Summarize validation activities
Summarize verification activities
Summarize commissioning activities
Summarize revalidation activities
Summarize reverification activities
Summarize recommissioning activities
Write change controls
Support Maintenance departments
Support Engineering departments
How You'll Work.
Team & Collaboration
Client Tech Transfer projects
Communication Scope
Technical documents
Full Job Description
COMPANY DESCRIPTION: A career here is life-enhancing. At Syner-G, we enable our people to build careers that impact positively on their quality of life. Through our expertise, insight, consulting and management skills, we accelerate breakthrough science and delivery of life-enhancing therapies to more patients. We work across a diverse range of clients and projects, supporting many organizations from the most critical phases of the drug discovery and approval process through to commercialization. It is meaningful, varied and thought-provoking work with a strategic emphasis, a solutions-driven approach and significant, real-world outcomes, from science to delivery/success. To learn more about who we are and what drives us, watch our company video here. Underpinning this mission is a culture that aligns perfectly with what we want to achieve. We enable our people to grow, we support them in their learning and we reward them in so many different ways. In return, they play an instrumental role in maintaining our reputation across the globe as a strategic biopharma product development and delivery partner. Syner-G was recently honored with BioSpace's prestigious "Best Places to Work" 2026 award, for the third consecutive year, along with many other award-winning programs to make a career here truly life-enhancing. These recognitions are a testament to our commitment to fostering a positive and engaging work environment for our employees, with a particular emphasis on culture, career growth and development opportunities, financial rewards, leadership and innovation. At Syner-G, we recognize that our team members are our most valuable asset. Join us in shaping the future, where your talents are valued, and your contributions make a meaningful impact. For more information, visit www.Synergbiopharma.com POSITION OVERVIEW: Syner-G is seeking a Validation Engineer to assist with the development and execution of validation protocols for various types of processes. The Validatio
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