Coord 1, R&D Document Mgmt

  • Sector: MRS Medical
  • Contact: Marie Nellas
  • Client: Medical Recruitment Strategies
  • Location: Warwick, United States of America
  • Salary: Negotiable
  • Expiry Date: 15 August 2022
  • Job Ref: BBBH401929_1660152452
  • Contact Email: mnellas@medicalrecruitmentstrategies.com

Job Title - Coord 1, R&D Document Mgmt

Job Description -

This is not a remote role the candidate must be available to commute to the Warwick site when necessary . 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 - bull Develops and modifies labeling for product labels cartons graphics inserts and other related material with supervision. bull Works with cross functional teams to verify labeling compliance. bull Supports labeling team collecting or transferring labeling information between templates or software systems. bull Develops and manages labeling changes within the approved document management system. bull 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. bull Manage multiple concurrent deadlines and prioritizes work as needed. bull 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. bull 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. -- Location - Warwick RI Remote/on-site hybrid: Ability to be on-site as projects require.