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The individual should be a motivated self-starter eager to contribute to building a manufacturing operation unparalleled in its capabilities and expertise, have a willingness and aptitude for adoption of new technology, an ability to build relationships and work effectively in a cross-functional team, and commitment to the highest safety and quality standards.
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Ideally LED lighting and/or electro-mechanical assembly manufacturing experience. Demonstrated expertise in lean manufacturing principles, Six Sigma, and continuous improvement methodologies for LED lighting and complex assemblies.
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As a Specialist, working on the QC Analytics team within Cell Therapy Manufacturing organization is responsible for sample management and testing to support the manufacturing of investigational medicinal products (IMP) utilized in Takeda clinical studies.
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Experience with clinical phase ATMP and Cell Therapy drug product manufacturing and QC testing. Find new, creative paths to solve difficult and important problems. This role will provide QA oversight of the quality control bioassay and flow cytometry laboratories along with raw material, analytical development, and supply chain groups in support of Vertex Clinical Cell and Gene Therapy Programs.
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15+ years of experience in biologics drug development or manufacturing in biotech or biopharma industry, with significant hands-on experience in areas of downstream process development and tech transfer, BLA enabling study and PPQ, commercial manufacturing, commercial supply, and product life cycle management.
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Perioperative RN Training Program - Designed for New Graduate RNs interested in transitioning to the Main Operating Room. Job Description - Nurse, Staff, New Grad TPP OR (3303574) Perioperative RN Training Program - Designed for New Graduate RNs interested in transitioning to the Main Operating Room.
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Direct the planning and implementation of process development, scale-up, technology transfer, and validation efforts in drug substance manufacturing, ensuring strategic alignment and operational excellence.
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Qualified candidates must have a PhD in synthetic/organic chemistry or related scientific field with 15+ years’ experience in drug substance development and manufacturing and a proven track record in developing and scaling up chemical process to kilo lab, pilot plant and commercial plant scales.
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Extensive experience selecting and overseeing CDMO’s for tech transfer of protein manufacturing including both upstream and downstream methods. Tech transfer of methods and processes to CDMO for early stage clinical manufacturing.
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How you will contribute: As a Specialist, working on the QC Analytics team within Cell Therapy Manufacturing organization is responsible for sample management and testing to support the manufacturing of investigational medicinal products (IMP) utilized in Takeda clinical studies.
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The GE Aerospace manufacturing site in Lynn designs, produces, assembles, and tests military and commercial aircraft engines and components. In this role the engineer will be the hardware owner of components, solving problems that arise in the manufacturing or operation of helicopter engine components through design changes, calculations, and investigations.
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You are excited about leading the development of innovative CMC regulatory strategies and the preparation and submission of high-quality CMC sections of INDs and CTAs, in close collaboration with regulatory team members, our in-house CMC and Quality teams, contract manufacturing organizations, external experts, and global health authorities.
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U.S. based employees are also eligible to receive, per calendar year, up to 80 hours of sick time, and new hires are eligible to accrue up to 120 hours of paid vacation. Provide direction for the identification of new targets aligned with the iDAS (integrated disease area strategy) in collaboration with the Oncology Development Therapeutic Area Unit and the Oncology Business Unit. Provide significant input into overall ODDU portfolio and department strategy Provide leadership and strategic support across Research, and/or to external collaborators.
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As a Client Account Manager for our Transportation Practice in New England, you will have the opportunity to impact strategic business relationships with key clients to assure Jacobs has sustained client relationships to achieve client satisfaction, and fully leverage the relationship to benefit the clients and the firm.
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New Hampshire Wetland Scientist certification a plus. Since 1978, Hancock Associates has been providing land surveying, civil engineering and wetland science services throughout Massachusetts, New Hampshire, Connecticut and Rhode Island.
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manufacturing new jobs Company: Jacobs in Boston, MA
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