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Amgen is currently seeking a Process Development Sr Principal Scientist in our Pivotal Attribute Sciences Department in Cambridge, MA. This team plays a crucial role in pivotal phase analytical development, including method development, validation, transfer, process and product development support, and GMP testing of drug substances and drug products.
$182,988 a yearFull-timeExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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Demonstrable flexibility and adaptable work ethic H&S Level 1 responsibility statement Willingness to embrace change and improve processes a systems develop Practical experience of Extrusion manufacturing process What Orbia Building & Infrastructure offers Do you want to make a difference by working with a purpose.
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This role requires a high level of expertise in stem cell biology, process engineering, and project management, ensuring the successful development and implementation of cell therapy manufacturing processes.
$40 an hourFull-timeExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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Deep expertise and industry experience in cell therapy process development principals including DOE and experience with current technologies in PSC process development and manufacturing, particularly scalable stem cell culture systems such as bioreactors.
$340,000 a yearFull-timeExpandApply NowActive JobUpdated 28 days ago - UpvoteDownvoteShare Job
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Prior hands-on experience with cell therapy process equipment is preferred. Our innovation and value-driven organization seeks to hire a Senior Research Associate with industry experience to join our rapidly growing Process Development team.
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Proficient with software tools and systems used for statistical process control, and reliability and failure analysis, including yield improvement. Join our team at the Draper microfabrication facility as a Microfabrication Process Engineer.
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A core element of Evergreen Health Hospice is our goal of continuous improvement in clinical quality, and we actively encourage staff participation in process improvement projects and, most importantly, allow our staff the time to provide exceptional care for our patients.
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The Process Research (PR) group within Synthetic Molecule Process Development (SMPD) is a global team responsible for interfacing with Takeda’s Discovery functions (e.g. medicinal chemistry, DMPK, Drug Safety) with the goal of route identification and phase appropriate route development to deliver GLP Tox and Ph 1 GMP Drug Substance (DS.
$170,500 a yearFull-timeExpandApply NowActive JobUpdated 8 days ago - UpvoteDownvoteShare Job
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Extensive experience in process chemistry development, scale-up, tech transfer and process characterizations, as well as deep understanding of GMP/GLP regulations. Significant demonstrated expertise in process chemistry and early and late stages API manufacturing and ability to coordinate CDMO activities in the development and commercialization of pharmaceutical products.
Full-timeExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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Lead internal process development, optimization and tech transfer of upstream and downstream process development for clinical development pipeline. Vice President Head of CMC and Process Development (Biologics) 2030201.
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The Senior Director, Chemical Process Development and Manufacturing will design, execute, and lead chemical process development and manufacturing strategy to produce drug substances for GLP toxicology, clinical supplies and potential commercialization.
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This Sustaining Process Engineer/Technician will be working in the Process Engineering Group at Skyworks in Woburn, MA, to support and develop wafer fabrication processes that produce RF and mobile communication devices including HBT, BiFET, pHEMT, BiHEMT, and GaN at various performance nodes.
$111,900 a yearFull-timeExpandApply NowActive JobUpdated 20 days ago - UpvoteDownvoteShare Job
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Experience with process optimization, lean manufacturing, and continuous improvement methodologies. Drive a culture of continuous improvement, encouraging the identification and implementation of process enhancements.
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Lead bench-scale early and late phase process development activities and optimization of AAV purification process steps (chromatography, filtration, UF/DF) Experience authoring technical documents (process development, tech transfer, batch records, IND supporting documents) and supporting drafting of CMC sections of regulatory submissions (IND, IMPD, BLA.
$163,000 a yearFull-timeExpandApply NowActive JobUpdated 8 days ago - UpvoteDownvoteShare Job
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The Industry Process Consulting Intern will collaborate with people in leadership, marketing, sales and product management to support and help promote the future of CAD applications and SOLIDWORKS technology for engineers.
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process job Title: improvement Company: Darling Ingredients in Cambridge, MA
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