Precision QA Labeling Specialist - Regulatory Compliance

LGC; Milford (MA); On-site; USD 55,000 - 82,000; Full time

Job summary

LGC is seeking a QA Labeling Specialist to join our engineering team in the United States. You will generate and approve QA labeling documents, review IFUs, and ensure compliance with regulatory standards across products and changes.

Ideal candidates have a bachelor’s degree, 2+ years in regulated medical products, and strong MS Office skills along with labeling software proficiency. The role emphasizes accuracy, collaboration, and adherence to health and safety guidelines.

Qualifications

• Bachelor’s Degree or equivalent experience in a relevant field.
• Minimum of 2+ years of industry experience working in a regulated medical product environment.
• Proficient in Microsoft Word, Excel, Adobe InDesign and/or NiceLabel Pro software.

Responsibilities

• Generate, review, and approve all QA Labeling documentation with outstanding attention to detail.
• Support all QA labeling projects for the introduction of new products, product improvements, and labeling master document changes.
• Review and approve lot-specific production labeling to guarantee perfect adherence.
• Populate, review, and approve instructions for use (IFU) including lot-specific technical data when relevant.
• Complete, examine, and authorize IFU templates containing the revised lot-specific technical information.
• Populate, review, and approve lot-specific technical data and upload it to the relevant technical or resource library.

Skills

Regulated medical product experience

Written communication

Detail-oriented

Education

Bachelor’s Degree or equivalent

Tools

Microsoft Word

Microsoft Excel

Adobe InDesign

NiceLabel Pro

Job description

LGC is seeking a QA Labeling Specialist to join our engineering team in the United States. You will generate and approve QA labeling documents, review IFUs, and ensure compliance with regulatory standards across products and changes.

Ideal candidates have a bachelor’s degree, 2+ years in regulated medical products, and strong MS Office skills along with labeling software proficiency. The role emphasizes accuracy, collaboration, and adherence to health and safety guidelines.