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 Senior Validation Engineer to lead GMP validation programs across equipment, facilities, utilities, computerized systems, and manufacturing processes supporting biopharmaceutical development and delivery projects.
Syner-G is seeking a Contract Recruiter for a three-month engagement to build pipelines and recruit specialized Technical Operations and Engineering talent across the biotechnology, pharmaceutical, and life sciences industries.
Syner-G BioPharma Group is seeking a client-facing Consultant I to lead CMC program execution and clinical supplies planning across pharmaceutical development projects from early development through commercialization.
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 Senior Talent Acquisition Specialist to lead end-to-end recruitment for India-based roles while partnering with leaders across the business to support workforce planning and hiring needs.
