Takeda
Pursuant to Section 20 C.F.R. 656.10, you are hereby notified that an application for Alien Employment Certification will be filed by Takeda Development Center Americas, Inc. for the following job opportunity:
Job Location:
Cambridge, MA Position:
Scientist, Synthetic Molecule Process Development Position Description:
Takeda Development Center Americas, Inc. is seeking a Scientist, Synthetic Molecule Process Development with the following duties: Provide theoretical/conceptual input to the design, development, and execution of research assignments for a specific project or projects within the functional area (pipeline or non-pipeline); Independently plan and execute complex experiments, searching for novel approaches and methodologies to solve complex technical challenges; Plan and coordinate work with departmental and cross-functional peers (within and outside Pharm Sci) with an understanding of project timelines/deliverables; Maintain and build relationships with existing key vendors; Proactively analyze manufacturing issues and coordinate potential solutions with the CMC (Chemistry, manufacturing, and controls) team; Assist in the technical aspects of negotiation with vendors; Develop and implement novel approaches and tools for data collection, management, engineering, analysis, modeling, and interpretation; Review, interpret data, and communicate results with Pharm Sci functions and CMC team; Plan and implementation of solutions to project problem/issues; Communicate activities from their functional area to project teams (pipeline, non-pipeline, and functional initiatives) and request functional area action from the project teams to senior leaders in their functional area. Requirements:
PhD degree in organic chemistry or related field. Prior experience must include: Utilize lab equipment and operations by using the following techniques: NMR spectroscopy, chromatography (TLC, GC, HPLC), Infrared (IR) Spectroscopy, and Karl Fischer titration. Manage one’s time within individual, departmental, and corporate goals and timelines; coordinate and oversee internal and external resources (vendors) to ensure project milestones are met within designated schedules and budgets. Troubleshoot critical issues or problems in a synthetic route in a lab scale, pilot plant scale, and manufacturing scale, and determine causes and propose possible solutions. Document and communicate technical findings and concerns clearly within a team, utilizing concise language tailored to colleagues and supervisors; prepare documentation detailing identified issues in measurable terms for submission to internal stakeholders; adapt communication styles to effectively relay information to diverse audiences, including supervisors; author internal technical documents, such as Standard Operating Procedures (SOPs) and reports, adhering to organizational and regulatory standards. Full time. $128,800 - $208,600 per year. Competitive compensation and benefits. Takeda is an equal opportunity employer. Any individual may provide documentary evidence bearing on this application, with information on available workers and information on wages and working conditions, to the Certifying Officer, U.S. Department of Labor, Employment and Training Administration, Office of Foreign Labor Certification, 200 Constitution Avenue, NW, Room N-5311, Washington, DC 20210.
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Cambridge, MA Position:
Scientist, Synthetic Molecule Process Development Position Description:
Takeda Development Center Americas, Inc. is seeking a Scientist, Synthetic Molecule Process Development with the following duties: Provide theoretical/conceptual input to the design, development, and execution of research assignments for a specific project or projects within the functional area (pipeline or non-pipeline); Independently plan and execute complex experiments, searching for novel approaches and methodologies to solve complex technical challenges; Plan and coordinate work with departmental and cross-functional peers (within and outside Pharm Sci) with an understanding of project timelines/deliverables; Maintain and build relationships with existing key vendors; Proactively analyze manufacturing issues and coordinate potential solutions with the CMC (Chemistry, manufacturing, and controls) team; Assist in the technical aspects of negotiation with vendors; Develop and implement novel approaches and tools for data collection, management, engineering, analysis, modeling, and interpretation; Review, interpret data, and communicate results with Pharm Sci functions and CMC team; Plan and implementation of solutions to project problem/issues; Communicate activities from their functional area to project teams (pipeline, non-pipeline, and functional initiatives) and request functional area action from the project teams to senior leaders in their functional area. Requirements:
PhD degree in organic chemistry or related field. Prior experience must include: Utilize lab equipment and operations by using the following techniques: NMR spectroscopy, chromatography (TLC, GC, HPLC), Infrared (IR) Spectroscopy, and Karl Fischer titration. Manage one’s time within individual, departmental, and corporate goals and timelines; coordinate and oversee internal and external resources (vendors) to ensure project milestones are met within designated schedules and budgets. Troubleshoot critical issues or problems in a synthetic route in a lab scale, pilot plant scale, and manufacturing scale, and determine causes and propose possible solutions. Document and communicate technical findings and concerns clearly within a team, utilizing concise language tailored to colleagues and supervisors; prepare documentation detailing identified issues in measurable terms for submission to internal stakeholders; adapt communication styles to effectively relay information to diverse audiences, including supervisors; author internal technical documents, such as Standard Operating Procedures (SOPs) and reports, adhering to organizational and regulatory standards. Full time. $128,800 - $208,600 per year. Competitive compensation and benefits. Takeda is an equal opportunity employer. Any individual may provide documentary evidence bearing on this application, with information on available workers and information on wages and working conditions, to the Certifying Officer, U.S. Department of Labor, Employment and Training Administration, Office of Foreign Labor Certification, 200 Constitution Avenue, NW, Room N-5311, Washington, DC 20210.
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