Document Control Specialist

A Document Control Specialist job in Redwood City, CA is available through Adecco Medical and Science. We are searching for a Document Control Specialist who is responsible for authoring, revising and processing Standard Operating Procedures (SOPs) and other GMP related documentation in the manufacturing of CRISPR products and services as part of an overall document creation and harmonization project.

Responsibilities:

Support the Document Control Management System
Collaborate with Subject Matter Experts in the lab and amongst cross- functional teams to ensure that their input is obtained as part of the document writing activities
Translates process maps or other process representations and applies them to SOP procedures
Contributes to the maintenance and updates of the SOPs through harmonization tracking spreadsheets and is able to meet aggressive timelines
Ensure all controlled documents are reviewed and released following established procedures.


Requirements:

Excellent technical writing skills, with relevant SOP writing experience
Possess a solid understanding of document standards, criteria and conventions
GMP knowledge
Excellent verbal and written communication skills
Excellent analytical and problem-solving skills
Excellent interpersonal skills
Proficiency working in Microsoft Office applications
Knowledge of quality management systems
Good attention to detail
Able to work with minimal supervision



If you are interested in this Document Control Specialist job in Redwood City, CA then please click APPLY NOW. For other opportunities available at Adecco Medical and Science go to www.adeccousa.com. If you have questions about the position or would like more information, please contact Sindie Rothstein at 858-410-1108 or by email at Sindie.rothstein@adeccona.com

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Reference number US_EN_2_108175_333044