Quality Labeling Specialist — Global Impact

Lgc-Clinical-Diagnostics; Milford (MA); On-site; USD 55,000 - 82,000; Full time

Job summary

LGC Clinical Diagnostics, based in Massachusetts, seeks a QA Labeling Specialist to enforce quality and regulatory standards within the engineering team. You will handle labeling documents, IFUs, and master labeling with strict accuracy and regulatory alignment.

The role requires a bachelor’s degree and 2+ years in a regulated medical-product setting, plus proficiency in Word/Excel and labeling tools such as NiceLabel Pro. This on-site position supports product launches and labeling changes.

Qualifications

• Minimum of 2+ years of industry experience 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.
• Process all updated labeling documents through ETQ with proven accuracy.
• Update, review, and approve changes to the master labeling documents, including labels, packaging specifications, and IFUs.
• Complete verification of master labeling IFU updates on the auto-population electronic IFU software system.
• Upload QA labeling documents and customer communications to the relevant technical or resource library and website.
• Collaborate with applicable functional areas on build control and change control projects related to QA labeling.
• Keep designated areas clean and orderly while adhering closely to all workplace health and safety regulations.
• Perform other related duties as assigned by management.

Education

Bachelor’s Degree or equivalent in relevant field

Tools

MS Word

Excel

Adobe InDesign

NiceLabel Pro

Job description

LGC Clinical Diagnostics, based in Massachusetts, seeks a QA Labeling Specialist to enforce quality and regulatory standards within the engineering team. You will handle labeling documents, IFUs, and master labeling with strict accuracy and regulatory alignment.

The role requires a bachelor’s degree and 2+ years in a regulated medical-product setting, plus proficiency in Word/Excel and labeling tools such as NiceLabel Pro. This on-site position supports product launches and labeling changes.