Regulatory Labeling Specialist
Scientific Search, Plymouth Meeting, PA, United States
Contract Position
Are you ready to take ownership of global medical device labeling strategy in a highly regulated environment? My client is seeking a Contract Regulatory Labeling Specialist to drive compliance, accuracy, and innovation across product labeling, packaging, and documentation. This is a high-impact role where your expertise will directly support patient safety, regulatory excellence, and operational success. Location:
Plymouth Meeting, PA Why You Should Apply
6–12+ month contract with strong potential for extension High-visibility role partnering across Regulatory, Quality, Operations & Manufacturing Opportunity to lead ISO 15223-1:2021 symbol implementation and UDI strategy Work on globally distributed medical devices under FDA & EU MDR What You’ll Be Doing
Develop and execute global labeling strategies (FDA, EU MDR, international markets) Oversee labeling compliance across packaging, IFUs, and SDS Lead UDI and barcode implementation across product lines Review and approve labeling content, artwork, and technical documentation Establish labeling quality control procedures and governance standards Partner with suppliers and cross‑functional teams to ensure consistency and compliance Drive continuous improvement using production data, complaints, and regulatory updates About You
Bachelor’s degree in Regulatory Affairs, Life Sciences, Engineering, or related field Strong knowledge of 21 CFR Part 801, EU MDR, ISO 13485, ISO 15223-1:2021 Experience managing UDI requirements and barcode systems Skilled in reviewing IFUs, packaging artwork, and document control systems RAC certification or audit/inspection support experience preferred How To Apply
We’d love to see your resume, but we can start a conversation. Send an email to tori@scientificsearch.com, tell us why you’re interested, or feel free to email your resume. Please include Job#19756.
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Are you ready to take ownership of global medical device labeling strategy in a highly regulated environment? My client is seeking a Contract Regulatory Labeling Specialist to drive compliance, accuracy, and innovation across product labeling, packaging, and documentation. This is a high-impact role where your expertise will directly support patient safety, regulatory excellence, and operational success. Location:
Plymouth Meeting, PA Why You Should Apply
6–12+ month contract with strong potential for extension High-visibility role partnering across Regulatory, Quality, Operations & Manufacturing Opportunity to lead ISO 15223-1:2021 symbol implementation and UDI strategy Work on globally distributed medical devices under FDA & EU MDR What You’ll Be Doing
Develop and execute global labeling strategies (FDA, EU MDR, international markets) Oversee labeling compliance across packaging, IFUs, and SDS Lead UDI and barcode implementation across product lines Review and approve labeling content, artwork, and technical documentation Establish labeling quality control procedures and governance standards Partner with suppliers and cross‑functional teams to ensure consistency and compliance Drive continuous improvement using production data, complaints, and regulatory updates About You
Bachelor’s degree in Regulatory Affairs, Life Sciences, Engineering, or related field Strong knowledge of 21 CFR Part 801, EU MDR, ISO 13485, ISO 15223-1:2021 Experience managing UDI requirements and barcode systems Skilled in reviewing IFUs, packaging artwork, and document control systems RAC certification or audit/inspection support experience preferred How To Apply
We’d love to see your resume, but we can start a conversation. Send an email to tori@scientificsearch.com, tell us why you’re interested, or feel free to email your resume. Please include Job#19756.
#J-18808-Ljbffr