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Author Jobs in Ohio

1 - 15 of 39
1 - 15 of 39
Search Results - Author Jobs in Ohio
Germer International - Pharmaceutical Recruiting-Dayton
on process capability, yield, cycle time, and product quality.  •  Author, review and approve batch records, master manufacturing instructions, SOPs, and technical reports Qualifications:  •  Bachelor’s degree in Engineering, Pharmaceutical Sciences...
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Technifab, Inc.-Avon (OH)
sponsorship. Candidates must be legally author Please note that this position does not provide sponsorship for employment authorization. Candidates must be legally authorized to work in the United States....
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Belcan, LLC-Cincinnati
senior engineers.  •  Requirements & Traceability o Author, refine, and maintain software requirements and low-level design with traceability in DOORS/DNG or CAMEO. o Ensure bi-directional traceability from requirements to design, code, and tests...
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US Tech Solutions-New Albany (OH)
gains. Quality and Document Management Systems:  •  Able to author and manage various documents/protocols/reports  •  Deviation/CAPA/EV Owner  •  Change Control Owner Relationships:  •  Build networks with commercial and clinical operations.  •  Provide...
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Technifab, Inc.-Avon (OH)
be legally author Please note that this position does not provide sponsorship for employment authorization. Candidates must be legally authorized to work in the United States....
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Takeda Pharmaceutical-Cambridge
topics, as applicable.  •  Develop/author and execute global regulatory strategies for complex strategies. May oversee execution.  •  Monitor and anticipate trends that impact both the regulatory and access environments to strengthen product development plan...
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Germer International - Pharmaceutical Recruiting-Dayton
initiatives focused on process capability, yield, cycle time, and product quality.  •  Author, review and approve batch records, master manufacturing instructions, SOPs, and technical reports Qualifications:  •  Bachelor’s degree in Engineering, Pharmaceutical...
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Takeda Pharmaceutical-Cambridge
topics, as applicable.  •  Develop/author and execute global regulatory strategies for complex strategies. May oversee execution.  •  Monitor and anticipate trends that impact both the regulatory and access environments to strengthen product development plan...
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US Tech Solutions-New Albany (OH)
gains. Quality and Document Management Systems:  •  Able to author and manage various documents/protocols/reports  •  Deviation/CAPA/EV Owner  •  Change Control Owner Relationships:  •  Build networks with commercial and clinical operations.  •  Provide...
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Takeda Pharmaceutical-Cambridge
on product specific value evidence topics, as applicable.  •  Develop/author and execute global regulatory strategies for complex strategies. May oversee execution.  •  Monitor and anticipate trends that impact both the regulatory and access environments...
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OSAAVA Services-Columbus
Responsibilities  •  Develop and maintain SysML models using Cameo Systems Modeler  •  Author and maintain BDD, IBD, Activity, Sequence, and Parametric diagrams  •  Support DoDAF / UAF architecture development and modeling activities  •  Maintain model repositories...
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ASM International-Cleveland
support in the acquisition, tracking, and processing of content for publications developed by the Content Development group for the ASM technical journals.  •  Answer queries from ASM staff, member technical editorial staff, reviewers, and authors...
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Bowling Green (OH)
review and assist to author or edit work instructions as is needed.  •  acts as a Learning Systems Administrator to provide/create content, track, and assign trainings with the Vector Leanring Management platform and ADP learning platform.  •  maintain...
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icims.com -
Takeda Pharmaceutical-Cambridge
on product specific value evidence topics, as applicable.  •  Develop/author and execute global regulatory strategies for complex strategies. May oversee execution.  •  Monitor and anticipate trends that impact both the regulatory and access environments...
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Takeda Pharmaceutical-Cambridge
topics, as applicable.  •  Develop/author and execute global regulatory strategies for complex strategies. May oversee execution.  •  Monitor and anticipate trends that impact both the regulatory and access environments to strengthen product development plan...
Read more
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