- Merck & Co. (Rahway, NJ)
- …a motivated scientist with technical expertise in Biologics Potency assays in drug Development. More specifically, the ideal candidate will be a recognized expert ... assays for the development of therapeutic proteins, monoclonal antibodies, antibody- drug conjugates, and/or new modality-based products.-- The successful candidate… more
- Tris Pharma (Monmouth Junction, NJ)
- …Procedures (SOPs), current Good Manufacturing Practices (cGMPs), Food and Drug Administration (FDA) standards and batch record specifications.The incumbent uses ... mentors direct reportsAny other assignments determined by Quality managementRequirementsMinimum education and years of relevant work experience:Bachelors degree in… more
- Merck & Co. (Rahway, NJ)
- …Quality.As part of Our Company's Manufacturing Division, within the Biologics Drug Substance Commercialization (BDSC) organization, the upstream process science and ... and biologics. The group supports various cell bank and upstream drug substance process commercialization activities and second generation process development… more
- Aequor (Athens, GA)
- …responsibility for programs such as biosecurity, hazardous shipping, supply systems, controlled drug inventories, and other site or multi-site needs at direction of ... is by no means complete and may be changed or updated as needed. Education /Qualification Addendum: This person should either already possess or be willing to obtain… more
- Eisai, Inc (Exton, PA)
- …focused on the technology transfer, scale-up, and optimization of validatable biological Drug Substance (DS) / Antibody Drug Intermediate (ADI) production ... and to ensure the successful transfer of new products in development. Requirements Education : BS, MS or PhD in biological sciences or engineering Ph.D. with 8… more
- Merck & Co. (North Wales, PA)
- …statistical programming activities for multiple and/or late stage drug /vaccine clinical development projects. -Accountability predominantly includes the development ... includes outsource provider staff.Membership on departmental strategic initiative teams Education and Minimum Requirement :BA/BS in Computer Science, Statistics,… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …external data acquisition and validation, and tools to support project portfolio across drug programs. This role is responsible for ensuring the quality and timely ... programming, reporting, external data acquisition, processing, and validation activities for drug programs under the outsourcing and in-house operating models. Is… more
- Merck & Co. (Rahway, NJ)
- …supported by publications and external presentations is expected.-Qualifications- Education Minimum Requirements:Ph.D. in analytical chemistry/biochemistry or related ... of actions.Experience in analysis of various Biologic modalities (eg, mAb, antibody- drug conjugate, fusion protein).Knowledge and experience in Antibody Drug … more
- Merck & Co. (Rahway, NJ)
- …Practices (GMP) activities such as release, stability, and in-process testing of Biologics Drug Substance (DS) and Drug Product (DP). - Act as subject ... on several factors including, but not limited to relevant education , qualifications, certifications, experience, skills, geographic location, government requirements,… more
- Merck & Co. (Rahway, NJ)
- …data standard deliverables for world-wide regulatory application submissions of drug and vaccine clinical development projects. Accountability predominantly includes ... stakeholdersPosition Specific Required Skills and Experience: US and/or worldwide drug or vaccine regulatory application submission experience including the… more
