Coord 1, R&D Document Mgmt
- Expired: over a month ago. Applications are no longer accepted.
Job Title Labeling Associate
Location Warwick, RI
Duration 12+ Months Contract
Client: Medical Device Company
Employment Type: Contract on W2 (Need US Citizens Or GC Holders Only)
-- Location Warwick, RI or Vernon Hills Remote/on-site hybrid: Ability to be on-site as projects require.
This is not a remote role the candidate must be available to commute to the Warwick site when necessary .
A strong focus on someone who has experience with labeling, project management and has a high potential for being converted to FTE.
The Associate works with Labeling team to design, test and manage labeling for BD Surgery products. The associate will work with label software and product labeling documentation within BDI Surgery, for both new and sustaining products. Activities may include but is not limited to project management, labeling design and development, translation service coordination, and implementation of labeling at any of the manufacturing sites.
-- Essential Duties, Position Responsibilities
Develops and modifies labeling for product labels, cartons graphics, inserts and other related material with supervision.
Works with cross functional teams to verify labeling compliance.
Supports labeling team collecting or transferring labeling information between templates or software systems.
Develops and manages labeling changes within the approved document management system.
Design product labeling with guidance from senior labeling team members but is able to troubleshoot such factors as product identification, aesthetic quality, printing, and production needs. Manage multiple concurrent deadlines and prioritizes work as needed.
Complies with the U.S. Food and Drug Administration (FDA) regulations, other regulatory requirements, Company Policies, Standard Operating Procedures (SOP), working instructions, and task assignments.
Performs other related duties and responsibilities, on occasion, as assigned.
-- Education and Experience -- Bachelor's degree in Art/Graphic Design preferred (Associates and/or experience will be considered in place of degree). 1+ year experience working in regulated industry with exposure to manufacturing (e.g., medical device or pharma). Experience with a label software (e.g., EasyLabel, NiceLabel, BarTender or enLabel). Experience designing and maintaining clinical labeling or marketing materials for regulated industry will be considered towards design experience. Experience utilizing design software and graphic tools such as, Adobe Illustrator, Photoshop, InDesign, Adobe Pro and other related software. Should have excellent organization, problem solving / troubleshooting skills, along with the openness to raise questions and ideas. Ability to communicate timely and effectively with team members and supporting services, regardless of location. Customer-service orientated with demonstrated ability to work on cross-functional teams with internal and external personnel. Basic English writing, editing skills along with good verbal communication skills. Flexibility to accommodate and manage changing priorities, deadlines, and project needs.
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