Remote Jobs at Syner-G BioPharma Group
Find your next remote opportunity · 2 Open Positions
Syner-G BioPharma Group provides in-depth expertise across the three key elements of Chemistry, Manufacturing, and Controls (CMC): Regulatory Services, Technical Development, and Quality/IT.
We call this CMC 360™.
We also provide medical writing services, with expertise in authoring a variety of regulatory documents across a wide range of therapeutic areas and in all phases of development.
Our regulatory affairs services include the development and implementation of global regulatory strategic plans, regulatory agency meeting support, and electronic submissions to regulatory authorities around the world.
We have the skill set and experience to guide your prime asset through any development challenges and along the ever-changing maze of regulatory filing pathways, to a position of full compliance, and high quality.
Our expertise spans small molecules, peptides, oligonucleotides, biologics, monoclonal antibodies, antibody-drug conjugates, and cell and gene therapy products.
Principal Process Engineer
Principal Process Engineer leading biopharma process development, automation, scale-up, and technology transfer at Syner-G. Providing strategic technical leadership across development, clinical, and commercial manufacturing programs.
Consultant I, Medical Writing
MWS Consultant I authoring regulatory documents, leading projects, and building client relationships at Syner-G. Requires advanced degree and 3 years of experience in medical writing and regulatory compliance.
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