QA Labeling Specialist

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

Job summary

LGC Clinical Diagnostics in Milford, MA is seeking a QA Labeling Specialist to join our engineering team and contribute to quality and compliance.

You will generate, review, and approve labeling documentation, support labeling projects for new products and changes, and ensure accurate lot-specific labeling and IFU templates. The role demands attention to detail, strong communication, and experience in a regulated medical product environment.

Qualifications

• Bachelor’s Degree or equivalent experience in a relevant field.
• Minimum 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 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.

Skills

Attention to detail

Troubleshooting

Communication

Education

Bachelor’s Degree or equivalent experience in a relevant field

2+ years regulated medical product experience

Tools

Microsoft Word

Excel

Adobe InDesign

NiceLabel Pro

Job description

Job Description

Are you ready to play a key role in ensuring quality and compliance in a world-class organization? At LGC, we are looking for a dedicated QA Labeling Specialist to join our ambitious engineering team. As a part of our growing community, you will contribute to projects that impact global health and safety standards. Join us and help us make a difference!

Duties:

• 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.

Qualifications:

Qualifications

Minimum 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.

Preferred Qualifications:

• Knowledge of FDA 21CFR820, ISO13485, IVDD98/79/EC, IVDR EU/2017/746, and international regulatory requirements.

Behavioural & Interpersonal Proficiencies:

• Resonate and operate in line with LGC’s core value behaviors: Passion, Curiosity, Integrity, Brilliance, and Respect.


• Promote cooperation and dedication within a team to achieve goals and deliverables.


• Strong initiative and troubleshooting skills required.


• Strong interpersonal skills and the ability to communicate well – verbally and in writing.


• Strong attention to detail combined with consistently precise work.


• Ability to multitask and determine priorities is essential.

Additional Information

The customary salary range for this position is:

Minimum pay rate : $55,000 USD

Maximum pay rate : $82,000 USD

The salary range provided covers the minimum and maximum amounts projected for this role. The base salary will be influenced by factors like experience, skills, and location.

All your information will be kept confidential according to EEO guidelines.

Join LGC and become part of a team that values collaboration, integrity, and brilliance in all we do. We are committed to encouraging a workplace where everyone can thrive and contribute to our mission.

Our values:

• PASSION


• CURIOSITY


• INTEGRITY


• BRILLIANCE


• RESPECT

Equal opportunities

LGC strongly believes that every job applicant and employee should be valued for their individual talents regardless of age, disability, race, color, ethnic or national origin, sex, sexual orientation, gender reassignment, marital or civil partnership, parental responsibilities, religion, or belief. Shortlisting, interviewing, and selection will always be carried out without regard to gender, sexual orientation, marital status, color, race, nationality, ethnic or national origins, religion or belief, age, or trade union membership.

This position requires current U.S. work authorization. We are unable to sponsor or assume sponsorship for temporary visas (including H-1B, H-2B, O-1, TN)

For more information about LGC, please visit our website www.lgcgroup.com

\\ #scienceforasaferworld

Compensation:

Compensation:
$55,000-$55,000 per year