Description:Create/Update, issue and distribute product artwork of current versions of QuarkXpress, CS5 including (Adobe Illustrator, Photoshop, InDesign etc.). Support routing and approval processes as required. Attend product launch meetings as required. Ensure artwork schedule adherence and provide communication regarding priorities.Responsible for compliance with applicable Corporate and Divisional Policies and procedures.1. Assess proposed artwork packages and take appropriate actions to create, update to currently indicated standards, proofing, pre-flight, and communicate with production sites to ensure electronic artwork for AMO labeling/packaging components meets AMO's graphic standards and release requirements. And other activities as define by management.2. Participate in project team development meetings and with third party design artwork suppliers to support the initiation of appropriate artwork meeting requirements to minimize rework and delays.3. Responsible to manage computer generated labeling formats and to ensure production validation activities are addressed before authorizing release for production use.4. Monitor actions and escalate issues to department and project team management regarding artwork releases to meet project plan deadlines.Requires a minimum of 2 years Production graphics experience in a quality or operational function, preferably in a medical device environment or similarly regulated environment. Must have capacity for attention to detail with the ability to recognize errors in spelling, punctuation, and grammar. Must be able to work independently as well as within a team. Good oral and written communication and strong organizational skills necessary. Able to manage multiple tasks and prioritize accordingly to meet challenging deadlines. Must exhibit flexibility in meeting constantly changing demands. Must have good customer focus with ability to influence internal and external groups. Must have experience with graphics programs, word processing, and database/spreadsheet programs and bar-code applications as currently utilized at AMO on both the Macintosh and PC platforms. Prior labeling development and proofreading experience is helpful.Production Artwork Tech. Instructions for use creation includes working with styles and formatting text in Adobe InDesign and Microsoft word. Label creation includes placing data and images onto a label template and transferring information into a database. Must have attention to detail. A very specific process must be followed to align with ISO and FDA regulations. Must have the ability to learn various software programs quickly. Applicant with in a quality background is desired. Entry level. Associates Degree or equivalent experience as a label designer in the Medical Device industry. Must be an expert in Adobe InDesign. Knowledge of Word, Excel, and Adobe Acrobat required. Must follow all procedures and regulations.Notes:8am - 5pm VIVA 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:Create/Update, issue and distribute product artwork of current versions of QuarkXpress, CS5 including (Adobe Illustrator, Photoshop, InDesign etc.). Support routing and approval processes as required. Attend product launch meetings as required. Ensure artwork schedule adherence and provide communication regarding priorities.Responsible for compliance with applicable Corporate and Divisional Policies and procedures.1. Assess proposed artwork packages and take appropriate actions to create, update to currently indicated standards, proofing, pre-flight, and communicate with production sites to ensure electronic artwork for AMO labeling/packaging components meets AMO's graphic standards and release requirements. And other activities as define by management.2. Participate in project team development meetings and with third party design artwork suppliers to support the initiation of appropriate artwork meeting requirements to minimize rework and delays.3. Responsible to manage computer generated labeling formats and to ensure production validation activities are addressed before authorizing release for production use.4. Monitor actions and escalate issues to department and project team management regarding artwork releases to meet project plan deadlines.
Requires a minimum of 2 years Production graphics experience in a quality or operational function, preferably in a medical device environment or similarly regulated environment. Must have capacity for attention to detail with the ability to recognize errors in spelling, punctuation, and grammar. Must be able to work independently as well as within a team. Good oral and written communication and strong organizational skills necessary. Able to manage multiple tasks and prioritize accordingly to meet challenging deadlines. Must exhibit flexibility in meeting constantly changing demands. Must have good customer focus with ability to influence internal and external groups. Must have experience with graphics programs, word processing, and database/spreadsheet programs and bar-code applications as currently utilized at AMO on both the Macintosh and PC platforms. Prior labeling development and proofreading experience is helpful.Production Artwork Tech. Instructions for use creation includes working with styles and formatting text in Adobe InDesign and Microsoft word. Label creation includes placing data and images onto a label template and transferring information into a database. Must have attention to detail. A very specific process must be followed to align with ISO and FDA regulations. Must have the ability to learn various software programs quickly. Applicant with in a quality background is desired. Entry level. Associates Degree or equivalent experience as a label designer in the Medical Device industry. Must be an expert in Adobe InDesign. Knowledge of Word, Excel, and Adobe Acrobat required. Must follow all procedures and regulations.
Notes:8am - 5pm
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