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Summary : The Scientist / Sr. Scientist in Process Development Department is responsible for monitoring and coordinating formulation activities. Support drug candidate design optimization, selection, validation, and stability study throughout pre-clinical and clinical purification process development for antibody/protein.
$90,000 - $120,000 a yearExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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The Product Development (PD) Senior Scientist I, under minimal guidance, designs, plans and conducts pre-formulation, formulation and process development activities as well as scale-up trials of complex projects using risk-based approach.
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Since integrating into Lundbeck in October 2019, Lu-SBP has supported commercial launch of Lundbeck's first biologic product (Vyepti) and advancement of a growing biologics pipeline in collaboration with our Copenhagen-based Process Science & Validation Team. The Lu-SBP team leads and supports the development of new product candidates from cell line development through commercial validation of Drug Substance and Drug Product manufacturing processes.
$145,000 - $165,000 a yearFull-timeExpandApply NowActive JobUpdated 3 months ago - UpvoteDownvoteShare Job
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10+ years Downstream Process Development experience related to biochemical engineering and/or protein biochemistry, scale-up principles, and manufacturing of Biopharmaceuticals (cGMP) Bachelor's degree and 15 years of Downstream Process Development experience.
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This leader will work closely with colleagues across Pharmaceutical Development, Medicinal Chemistry, and Safety Assessment, and Regulatory CMC to drive compound selection, chemical process development, formulation development, control and stability strategies to efficiently move compounds from late discovery through preparation for phase three manufacture.
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Process Development and Formulation Scientist – #6269. Qualifications include a BS in Chemistry, Pharmaceutical Science, Chemical Process Engineer or higher degree, 2-5 years of experience in a pharmaceutical related field is preferred.
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Demonstrated capability in plastic film formulation, lamination process, packaging applications and coating technology development. Leading teams working on adhesive formulation and development of new and improved products through the research and development stage.
$100,000 - $130,000 a yearFull-timeExpandApply NowActive JobUpdated 3 months ago - UpvoteDownvoteShare Job
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Drives and supervises the creation of the formulas and the day-to-day product development process as the key lead cross functionally, sourcing high quality and efficacious on-trend and clean raw materials.
Full-timeExpandApply NowActive JobUpdated 22 days ago - UpvoteDownvoteShare Job
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Industry giant seeks an experienced Process Development Scientist to develop protein purification processes to be scaled up and transferred into cGMP manufacturing including evaluation of transferred processes, transfer of processes to manufacturing, harvest clarification, normal flow filtration, purification, tangential flow filtration, and product final formulation.
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These Process Development teams are supported by Analytical Development and Formulation Development teams. Vaxcyte is looking for a Director/Associate Director with significant experience in early-stage fermentation development and late-stage Process Characterization (PC) to join the Polysaccharide process team.
$211,000 - $225,000 a yearFull-timeExpandApply NowActive JobUpdated 3 months ago - UpvoteDownvoteShare Job
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Responsible for performing formulation and process development activities associated with solid/liquid supplements. The formulation scientist reports directly to the Formulations Development Manager.
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Assigned across Analytical Development QC, Product Development (Formulation) Process Development and its. The Director is responsible for establishing and implementing best practices for generation and integration of product and process knowledge generation across the groups accountable for analytical testing, formulation, process development, process characterization and introduction of products into fill/finish operations.
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Strong scientific, technical interactions with partner organizations such as Process Development, Process Engineering, Supply Chain, Quality Control, Regulatory. Technical understanding of Drug Product (DP) manufacturing operations, such as buffer batching, DP formulation, DP Filling, Inspection.
TemporaryExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Responsible for GMP compliance in formulation and process development. Responsible for all formulation and process development of several ongoing projects including project management and customer contact.
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This role requires a strong technical background in biologic drug formulation, process development, manufacturing and drug delivery. ·Experience in DP development for commercialization including risk assessments, process characterization and validation.
Full-timeExpandApply NowActive JobUpdated 2 days ago
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