Remote Jobs at Syner-G BioPharma Group
Find your next remote opportunity · 3 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.
Director, Sales
Director of Sales at Syner-G leading territory strategy, driving new business generation and managing client relationships in biotech services.
Senior Project Engineer
Sr. Project Engineer supporting engineering and commissioning within GMP life sciences environments. Collaborating on project execution and ensuring compliance with regulatory requirements.
Validation Engineer
Validation Engineer ensuring compliance with internal quality standards in biopharma equipment and manufacturing processes. Supporting validation activities, tech transfer, and continuous improvement initiatives.
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