Finding the best job has never been easier
Share
Your role:
Work with internal and external customers to gather needs and requirements of labeling changes
Communicate gathered requirements to the design team and keep them informed of any late inputs/changes
Update and maintain all project logs, timeline management, and tracking through project life cycle.
Provide updates and status of design jobs to customers and project team through tracking, meetings, reports, etc. in a timely and detailed manner.
Review and proofread all packaging and labeling draft artwork to ensure accuracy while adhering to established company processes, Philips brand guidelines and labeling compliance standards.
You're the right fit if:
You’ve acquired 2+ years of experience in a medical device, pharmaceutical or regulated industry
Your skills include strong knowledge of global regulations, requirements and standards including 21 CFR Parts 803, 806 and 820; CFR 210/211, Cosmetic Products GMP, ISO 13485 and ISO 9001
You have a bachelor’s degree or equivalent experience
You must be able to successfully perform the following minimum Physical, Cognitive and Environmental job requirements with or without accommodation for this .
You’re a strong communicator with cross-functional partners
How we work together
This role is an office role.
We are a health technology company. We built our entire company around the belief that every human matters, and we won't stop until everybody everywhere has access to the quality healthcare that we all deserve. Do the work of your life to help improve the lives of others.
Learn more about .
Discover
Learn more about
Learn more about our commitment to .
US work authorization is a precondition of employment. The company will not consider candidates who require sponsorship for a work-authorized visa, now or in the future.
These jobs might be a good fit