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Frontage Laboratories is a CRO / Clinical Research Organization providing integrated, science-driven, product development services throughout the drug discovery and development process to enable life science companies to achieve their drug development goals.
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Scientist – Immunogenicity Full Time Exton PA or Spring House PA Frontage Laboratories Frontage Laboratories is a CRO / Clinical Research Organization providing integrated, science-driven, product development services throughout the drug discovery and development process to enable life science companies to achieve their drug development goals.
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Pharmaron is a premier contract research organization that offers a broad spectrum of R&D and manufacturing service capabilities throughout the entire drug discovery, preclinical, clinical development and commercialization process.
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The position provides counseling on clinical research, drug development and clinical trial matters, as well as the applicable laws and regulations and related guidance. The person in this role shall be responsible for providing legal counsel, drafting and negotiating agreements and documentations as supporting the various R&D units, from early research and discovery through the various clinical trial stages, and supporting related licenses and transactions.
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The role of Research Scientist, Drug Delivery & Nanotechnology involves leading and conducting experiments for the discovery and preclinical activities of Ocugens product pipeline related to nanoparticle-based drug substances.
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Frontage’s biologics teams have an average 10 – 15 years in complex drug development and have worked with large molecule applications throughout its evolution in product development. We can handle projects for a range of large molecule development projects including peptides, proteins, monoclonal antibodies, bispecific antibodies, biosimilars, oligonucleotides, biomarkers , and antibody drug conjugates.
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This position reports directly to the Principal Scientist, Drug Delivery & Nanotechnology. Support preclinical drug delivery platforms and nano-formulation efficacy studies related to ophthalmologic, neurodegenerative, and infectious diseases and clinical trial research as needed.
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The Associate GLP QA Auditor coordinates auditing activities to ensure compliance with SOPs and GLP requirements. Prepare and sign a statement to be included with the final GLP study report which shall specify the dates inspections were made and findings reported to management and to the study director.
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Conduct execution of separation-based analytical assays for biologics drug development to quantify purity, size variants, excipient content, charge variants, etc. Partner with various J&J collaborator groups, such as the API, DPD&D, LMAD, and Discovery, to ensure adoption and implementation of process improvements for the preparation of biologics for routine testing.
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Must pass a pre-employment drug screen testPreferred Skills, Knowledge & Experience:Corrections or law enforcement background. Confiscate illegal contraband and notify supervisory personnel immediately upon discovery.
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The Engineering, Director role is part of the global Drug Delivery Systems (DDS) team. Represents the device development function on CMC team and to coordinates directly with Quality, Regulatory, Commercial, Formulation, Drug Product Development (DPD), Analytical Development (AD), Sourcing, other members of DDS and other stakeholders to determine device requirements needed to develop device solutions and the execution of device /combo development.
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