Global Labeling Lead Specialist 
Kelly® Science & Clinical is seeking a Global Labeling Lead for our client based in Bridgewater, NJ. If you’re passionate about bringing the latest scientific discoveries to life and are ready to take the next step in your career, trust The Experts at Hiring Experts.
Length of assignment – 12-14 months  may extend
Day shift- Monday to Friday must be available to work EASTERN time zone hours

Ideally – HYBRID
Locations : Rochester, NY, Bridgewater, NJ, Greenville, SC, Tampa, FL or St Louis, MO 

Remote option possible

The Global Labeling Lead is responsible for leading labeling artwork development/ revisions projects for medical device products, and assessing changes in standards, regulations, and requirements to identify impact to product labels.  Manage and coordinate labeling change requests and content updates for US only artwork, MDD, MDR, new product launches, private label or regional/country specific lens/lens care.

Responsibilities:

• Work with regional/country requestors to initiate projects/changes.
  

• Liaise with cross-functional SME teams to verify and confirm labeling content.
  

• Perform label assessments using labeling processes, forms and checklists.
  

• Works to resolve any conflicts of reviewer feedback on labeling content
  

• Work closely with Label Requirement Specialist (LRS) Coordinator to align & interpret LRS into redline versions of artwork.
  

• Provides continuous feedback to LRS Coordinator on any content changes that would impact LRS updates.
  

• Attend LRS meetings with LRS Coordinator.
  

• Act as LRS Coordinator back-up; Redline and communicate changes with project team and disseminate information to the graphics team for artwork creation.
  

• Perform all assigned ELM project task submission artwork support
  

• Provides RA artwork support for health authority submissions; provides before/after artworks, redlined PDFs, etc.
  

• Monitors timelines and advises project teams of any impacts to timelines during TG1 SOP support/review.
  

• Participate in company audits, as needed

Requirements:

• Knowledge of medical device industry, regulatory affairs, as well as discipline throughout the product lifecycle including Development, Commercialization, and Operations.
  

• Previous experience Adobe Acrobat is required.
  

• Knowledge of standards and regulations relating to submissions and regulatory approval of device products.
  

• Knowledge of product labeling processes for review and obtaining regulatory approvals.
  

• Strong technology skills and abilities, especially with Microsoft Office programs and web-based programs.
  

• Ability to critically and efficiently review detailed information to support a labeling revision.
  

• Demonstrated ability in analytical reasoning and critical thinking skills.
  

• Ability to contribute and lead within a team environment
  

• Ability to understand and apply business drivers outside of Regulatory Affairs.
  

• Strong communication skills; both oral and written.
  

• Strong interpersonal skills with the ability to influence others in a positive and effective manner.
  

• Detail-oriented with the ability to proofread and check documents for accuracy and inconsistencies quickly and efficiently.
  

• Bachelor’s degree or higher preferred. In lieu of degree, 8 years of industry experience with applied knowledge of applicable standards, regulations of medical device labeling requirements.

Requirements What happens next
Once you apply, you’ll proceed to the next steps if your skills and experience look like a good fit. But don’t worry—even if this position doesn’t work out, you’re still in our network. That means all of our recruiters will have access to your profile, expanding your opportunities even more.
Helping you discover what’s next in your career is what we’re all about,
#P1
 

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