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Technical Writer

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Company: Techusa

Location: Lancaster, PA

Date Posted: August 4, 2014

Source: TechUSA

•Designs, creates, revises and maintains technical documentation for laboratory related documents (e.g. SOPs, protocols, lab equipment qualification protocols, etc). Utilize SME's, design specifications, users, system manuals etc. for guidance. 
•Interviews subject matter experts and the users of the processes as well as conduct research and have the ability to gather information to produce a clear concise document to the target audience 
•Form a clear understanding of the purpose of the document that needs to be created. 
•Gather information from existing process flow documents, equipment manuals and from subject matter experts. 
•Draft SOPs and explain in simple language scientific and technical ideas that are difficult for the average reader to understand. 
•Write the SOP in a concise, step-by-step, easy to read and follow format ensuring it is easy to follow and not ambiguous. 
•Edit, proofread, perform formatting of technical documents for business and consumers. 
•Determine if a Supplement/Form ...
•Designs, creates, revises and maintains technical documentation for laboratory related documents (e.g. SOPs, protocols, lab equipment qualification protocols, etc). Utilize SME's, design specifications, users, system manuals etc. for guidance. 
•Interviews subject matter experts and the users of the processes as well as conduct research and have the ability to gather information to produce a clear concise document to the target audience 
•Form a clear understanding of the purpose of the document that needs to be created. 
•Gather information from existing process flow documents, equipment manuals and from subject matter experts. 
•Draft SOPs and explain in simple language scientific and technical ideas that are difficult for the average reader to understand. 
•Write the SOP in a concise, step-by-step, easy to read and follow format ensuring it is easy to follow and not ambiguous. 
•Edit, proofread, perform formatting of technical documents for business and consumers. 
•Determine if a Supplement/Form or Work Instruction document is needed. WI contains much more detail than an SOP and is only created if very detailed instructions are needed. 
•Develop work Instructions that contains detailed instructions that specify exactly what steps to follow in order to complete an activity. 
•Communicate activities and results to team leads and site leads/stakeholders 
•Work closely with Site Quality to develop and report appropriate metrics. 
•Minimum of a bachelor's degree in a science and/or engineering related field preferred. 
•Minimum 3-4 years’ experience in a pharmaceutical or related industry. 
•Scientific training and fundamental understanding of quality control laboratories. (microbiological or analytical) , procedures and regulation.
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