Description: Writes a variety of technical articles, reports, brochures, and/or manuals for documentation for a wide range of uses.May be responsible for coordinating the display of graphics and the production of the document.Familiar with standard concepts, practices, and procedures.Relies on limited experience and judgment to plan and accomplish goals.A certain degree of creativity and latitude is required.May require a bachelor’s degree or 2-4 years of experience. This position is responsible for initiating and managing change control packages, primarily for device master records, to support product end-of-life documentation.The change control process may involve various document types, including Manufacturing Procedures, Quality Control Procedures, Certificates of Analysis, Material Specifications, and Labels/Package Inserts. Key responsibilities include:Creating thorough and well-drafted change impact assessment documents.Ensuring quality documents are properly redlined and in-process revisions are controlled before approval.Conducting detailed reviews of document changes before submission to supervisors or approvers.Ensuring all necessary documents for routing change requests are in place before approval.Ensuring documentation is appropriate, justified, and approved by responsible functional areas according to timelines and established procedures. Note:Onsite8am - 5pmVIVA is an equal opportunity employer. All qualified applicants have an equal opportunity for placement, and all employees have an equal opportunity to develop on the job. This means that VIVA will not discriminate against any employee or qualified applicant on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status
Description:
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Onsite
8am - 5pm
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