Syner G BioPharma Group offers leading CMC & Regulatory Affairs solutions for biopharma, specializing in strategic CMC 360 services, global regulatory affairs, and quality compliance to support successful drug development.
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Syner-G is seeking a Documentation Management Lead to support a major design and construction capital program by overseeing project documentation, information management, and records across multiple regulated workstreams.
Syner-G is hiring a Senior Validation Engineer to lead GMP validation activities for equipment, systems, facilities, and manufacturing processes in biotech and pharmaceutical environments.
Syner-G is seeking a Sr. Validation Engineer to lead GMP validation activities for biopharma equipment, systems, facilities, and manufacturing processes across internal and client projects.
Syner-G is hiring an Associate Director to lead US and Canadian promotional regulatory review for biopharma materials across launch and lifecycle activities.
Syner-G is hiring a business analyst to support the continuous improvement of its enterprise applications and data platform through requirements, administration, integrations, and reporting.
Syner-G is seeking a Staff Process Engineer / MSAT Technology Transfer Lead to manage a portfolio of monoclonal antibody drug substance technology transfers through GMP manufacturing, PPQ, and commercial readiness.
Syner-G BioPharma Group is seeking a remote Vice President, Biologics Development to lead West Coast market expansion while driving biologics consulting delivery and client development.
