Image Designer - Randstad USA

· Develop and maintain Instruction For Use (IFUs) documents, including product illustrations, layout design, and illustrative material and copy.

· Utilize existing templates in programs including, but not limited to, Bartender, Adobe LiveCycle and EnLabel to create or revise labeling artwork and content based on corporate graphic standards, procedures and/or previously established formats.

· Use of PLM (Windchill) for document control process to route all work for approval

· Perform prepress activities necessary to prepare labeling artwork files for accurate output.

· Prepare and route labeling packages for 1st article and approvals.

· Proofread labeling artwork utilizing measurement, inspection tools (e.g. rulers, barcode scanner, etc.) and related documentation. This is a quality role in medical devices which focuses on a first-time right approach. Attention to detail with minimal errors is key.

· Reviews and updates as necessary to ensure proper revision control and storage of all labeling.

· Establishes and cultivates a network of support (manufacturing, engineering, regulatory, legal, product development and marketing) to facilitate completion of labeling and artwork assignments.

· Can successfully work with cross-functional teams to address NCRs and CAPAs. Investigate, analyze, and identify root cause. Evaluate underlying issue and find long-term solutions.

· Maintains and follows proper compliance and quality system requirements. Ensures proper documentation is prepared and corrected to reflect continuous improvement activities that lead to new or improved processes.

 
location: Minneapolis, Minnesota
job type: Contract
salary: $60 - 70 per hour
work hours: 8am to 4pm
education: No Degree Required
 
responsibilities:

· Bachelor's degree or equivalent relevant experience required

· Proficient in Adobe Creative Suite and Microsoft Office

· Experience with Adobe Lifecycle is preferred

· Exposure to Bartender, EnLabel, Windchill and/or SAP is a plus

· Knowledge of Regulatory standards (FDA, EU MDR, Japan, Canada, ISO standards) is preferred

· Excellent written and verbal communication skills

· Ability to exercise independent judgment consistent with company policy

· Ability to organize and prioritize workflow

· Ability to interact with all levels of employees including senior management

· Ability to adapt to changing processes and learn programs/software quickly

· strong attention to detail is critical

• Experience level: Experienced
• Minimum 5 years of experience
• Education: No Degree Required