Labeling Specialist

Job Description

Job Description

Job Title: Labeling Specialist

Job Description

This role focuses on developing, managing, and maintaining medical device labeling using BarTender labeling software within a regulated environment. The Labeling Specialist ensures all labels meet regulatory, quality, and packaging requirements throughout the label lifecycle, while collaborating with cross-functional teams in a fast-paced, growth-oriented medical device organization.

Responsibilities

• Design, develop, and maintain medical device labels using BarTender labeling software in alignment with regulatory and quality requirements.
• Manage the full label lifecycle, including creation, review, revision, approval, and retirement of labeling content and formats.
• Author and update labeling content and related technical documentation to support medical device products and packaging.
• Collaborate with packaging engineering, regulatory affairs, quality assurance, and document control to ensure labels meet all functional, regulatory, and packaging needs.
• Support implementation requirements for new and existing labels, including integration with packaging design and manufacturing processes.
• Ensure labeling activities comply with medical device quality system standards, including ISO 13485 and 21 CFR 820.
• Use PLM and QMS platforms to route, track, and control labeling documents, changes, and approvals.
• Troubleshoot labeling issues and coordinate timely resolution with relevant stakeholders.
• Take ownership of assigned labeling projects and tasks, working independently while ensuring high accuracy and attention to detail.
• Proactively ask questions and seek clarification when encountering obstacles to maintain progress and quality.
• Contribute to continuous improvement of labeling processes, templates, and standards.
• Support audits and inspections by providing labeling documentation and demonstrating compliance with applicable regulations.

Essential Skills

• Hands-on experience with BarTender labeling software, including label design, configuration, and maintenance.
• Experience in medical device labeling, including understanding of regulatory requirements and label lifecycle management.
• Minimum of 4+ years of experience in medical device environments, working under ISO 13485 and 21 CFR 820 quality system requirements.
• Experience in labeling design and technical writing for medical devices, including instructions, warnings, and regulatory content.
• Experience supporting implementation requirements for labeling in coordination with packaging engineering and manufacturing.
• Exposure to packaging engineering, regulatory affairs, packaging design, quality assurance, document control, and labeling software in a regulated context.
• Familiarity with PLM and QMS platforms, with transferable skills from systems such as Agile or Windchill.
• Ability to work independently, take ownership of tasks, and deliver high-quality work with minimal supervision.
• Willingness to ask questions and collaborate with team members when encountering challenges.
• Strong attention to detail and accuracy in documentation and label content.

Additional Skills & Qualifications

• Direct experience with Agile PLM or Windchill systems.
• Experience working in a contract, consulting, or fast-paced project environment.
• Familiarity with FDA labeling regulations, including 21 CFR and Unique Device Identification (UDI) requirements.
• Knowledge of EU Medical Device Regulation (EU MDR) labeling requirements.
• Experience working within a formal document control environment for labeling and technical documentation.
• Strong written communication skills for clear and compliant technical writing.
• Ability to collaborate effectively with cross-functional teams in a medical device setting.

Work Environment

The role is based in a brand-new, modern medical device facility located in the Arber Lakes area, offering a spacious, well-organized environment with significant room for growth and expansion. The workplace emphasizes collaboration across product design, development, manufacturing, regulatory, quality, and packaging functions. The organization focuses on accelerating medical device product development and commercialization, creating a dynamic and fast-paced setting where adaptability and initiative are valued. Work is performed in a professional office and laboratory/manufacturing -adjacent environment that relies heavily on digital tools such as BarTender labeling software and PLM/QMS platforms. The culture encourages ownership, open communication, and proactive problem-solving, with opportunities to contribute meaningfully to new and ongoing medical device projects.

This is a Contract to Hire position based out of Maple Grove, MN.

The pay range for this position is $40.00 - $60.00/hr.

Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life & AD&D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave)

This is a fully onsite position in Maple Grove,MN.

This position is anticipated to close on Aug 10, 2026.

About Actalent

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.

The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email View email address on ziprecruiter.com for other accommodation options.

San Francisco Fair Chance Ordinance: Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records.

Massachusetts Lie Detector: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

Use of Artificial Intelligence (AI): We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.