Labeling Specialist

Hologic, Inc.

San Diego (CA)

On-site

USD 66,000 - 103,000

Full time

5 days ago
Be an early applicant
Application generator

A complete application in a minute — tailored resume and cover letter, ready to send.

Get past ATS filters

Benefits offered by this job

Annual bonus
Competitive salary

Job summary

Hologic, Inc. is seeking a detail-oriented Labeling Specialist to support labeling for GSS product portfolios.

You will serve as the labeling representative on cross-functional teams with Regulatory, Quality, Marketing, and Engineering to ensure labels, Instructions for Use, and related documents stay accurate, current, and compliant. This role requires experience in medical device labeling or regulated product documentation, ability to manage multiple projects, and coordination of reviews.

Qualifications

  • High school diploma or higher with relevant experience as listed.
  • Knowledge of QSR/GMP requirements is basic but essential.
  • Experience in print publishing, design, or document control.
  • Ability to manage multiple labeling projects and shifting priorities.

Responsibilities

  • Support labeling activities for assigned GSS product portfolios.
  • Represent Labeling on cross-functional product and project teams.
  • Drive labeling requirements for new product development and remediation projects.
  • Develop product labels and Instructions for Use using templates.
  • Prepare redlines and coordinate stakeholder reviews and approvals.
  • Track master labeling documents and update portfolio baselines.
  • Support label verification for accuracy and compliance before release.
  • Coordinate translations with internal teams or vendors.
  • Review translations against English source for accuracy.
  • Manage labeling deliverables through lifecycle systems.
  • Prioritize deliverables and communicate timelines and risks.

Skills

Strong communication
Cross-functional teamwork
Project/document management

Education

Bachelor’s degree with 0–2 years of related experience
Associate’s degree with 2–4 years of related experience
High School diploma with 4–6 years of related experience

Tools

Adobe Illustrator
InDesign
Agile PLM

Job description

Labeling Specialist

Louisville, CO, United States

San Diego, CA, United States

Newark, DE, United States

Marlborough, MA, United States

We are looking for a detail-oriented Labeling Specialist to support labeling activities for assigned GSS product portfolios. In this role, you will serve as the Labeling representative on cross-functional project teams and partner closely with Regulatory, Quality, Marketing, Engineering, and other stakeholders to ensure product labels, Instructions for Use, and related documentation remain accurate, current, and compliant.

This is a great opportunity for someone with experience in medical device labeling, document control, print publishing, or regulated product documentation who enjoys managing multiple projects, coordinating reviews, and improving processes. We are open to the following locations: CO, DE, MA, or SD

Key responsibilities
  • Support labeling activities for assigned GSS product portfolios.

  • Represent Labeling on cross-functional product and project teams.

  • Help drive labeling requirements for new product development, sustaining, and remediation projects.

  • Develop product labels and Instructions for Use using corporate templates and established document structures.

  • Prepare redlines for labeling changes and coordinate stakeholder review and approval cycles.

  • Track master labeling documents and updates to maintain accurate portfolio baselines.

  • Support label verification activities to confirm accuracy, consistency, and compliance before release.

  • Manage labeling deliverables through Agile or other product lifecycle management systems.

  • Coordinate translation activities with internal teams and external translation vendors.

  • Review translations against English source content for formatting and numerical accuracy.

  • Gather supporting documentation inputs from cross-functional teams for change orders.

  • Manage multiple labeling and documentation projects at the same time.

  • Prioritize deliverables, manage urgent requests, and communicate timelines, risks, and status clearly.

  • Contribute to process improvements, work instructions, style guides, templates, knowledge base topics, and department procedures.

  • Follow applicable procedures and quality system requirements.

Required Qualifications
  • High School diploma with 4–6 years of related experience, or

  • Associate’s degree with 2–4 years of related experience, or

  • Bachelor’s degree with 0–2 years of related experience.

  • Basic knowledge of QSR/GMP requirements.

  • Basic experience with print publishing, design, or document control programs.

  • Strong communication skills and ability to work with cross-functional teams.

  • Ability to manage multiple documentation projects and shifting priorities.

Preferred Qualifications
  • 4–6 years of related experience.

  • Proficiency with Adobe Illustrator and InDesign.

  • Familiarity with Agile Product Lifecycle Management.

  • Prior experience with surgical or interventional medical device labeling.

  • Experience supporting a product portfolio end-to-end, from label creation through lifecycle maintenance.

  • Experience coordinating documentation review cycles, change control, and translations.

So why join Hologic?

We are committed to making Hologic the company where top talent comes to grow. For you to succeed, we want to enable you with the tools and knowledge required and so we provide comprehensive training when you join as well as continued development and training throughout your career. We offer a competitive salary and annual bonus scheme, one of our talent partners can discuss this in more detail with you.

The annualized base salary range for this role is $65,900 - $103,000and is bonus eligible. Final compensation packages will ultimately depend on factors including relevant experience, skillset, knowledge, geography, education, business needs and market demand.

As part of our commitment to a fair and accurate evaluation of each candidate's qualifications, we require all applicants to refrain from using AI tools, such as generative AI or automated writing assistance, during any stage of the interview process. Responses influenced by AI may result in disqualification. We appreciate your understanding and cooperation in ensuring a transparent and equitable selection process.

Hologic, Inc. is proud to be an Equal Opportunity Employer inclusive of disability and veterans.

Get your free, confidential resume review.
or drag and drop your file here.
Similar jobs

Similar jobs worth comparing

Labeling Specialist
Labeling Specialist

Hologic, Inc. • Louisville (CO)

On-site
USD 66,000 - 103,000
Annual bonus
Competitive salary
Sr Manager, Regulatory Operations
Sr Manager, Regulatory Operations

Hologic, Inc. • Marlborough (MA)

On-site
USD 145,000 - 242,000
Sr. Design Assurance Engineer
Sr. Design Assurance Engineer

Hologic, Inc. • Town of Newark (WI)

On-site
USD 91,620 - 152,700
Lead Advanced Manufacturing Engineer
Lead Advanced Manufacturing Engineer

Hologic, Inc. • Louisville (CO)

On-site
USD 119,000 - 187,000
QA Labeling Specialist
QA Labeling Specialist

LGC • Milford (MA)

On-site
USD 55,000 - 82,000
Lead Advanced Manufacturing Engineer
Lead Advanced Manufacturing Engineer

Hologic, Inc. • Louisville (KY)

On-site
USD 119,000 - 187,000
Senior Labeling Specialist
Senior Labeling Specialist

Edwards Lifesciences • Irvine (CA)

On-site
USD 92,000 - 130,000
Competitive salaries
Performance-based incentives
Benefits programs
Sr. Design Assurance Engineer - Risk Management
Sr. Design Assurance Engineer - Risk Management

Hologic, Inc. • Marlborough (MA)

On-site
USD 97,000 - 153,000
QA Labeling Specialist
QA Labeling Specialist

LGC Group • Milford (MA)

On-site
USD 55,000 - 82,000
QA Labeling Specialist
QA Labeling Specialist

LGC Clinical Diagnostics • Milford (MA)

On-site
USD 55,000 - 82,000