Labeling Specialist
Moundsview, MN · On-site
Medtronic is a global leader in healthcare technology with a Mission to alleviate pain, restore ... Lead the creation, review, approval, and release of labeling components that support new product ...
Moundsview, MN · On-site
Medtronic is a global leader in healthcare technology with a Mission to alleviate pain, restore ... Lead the creation, review, approval, and release of labeling components that support new product ...
Moundsview, MN · On-site
Medtronic is a global leader in healthcare technology with a Mission to alleviate pain, restore ... Lead the creation, review, approval, and release of labeling components that support new product ...
Durham, NC · On-site
$128K - $358K/yr
... to the Global Regulatory Science Leadership Team, Project Development Teams and senior management, as relevant. * Provide input to the end-to-end labeling process. * Ability to lead and manage ...
Durham, NC · On-site
$128K - $358K/yr
... to the Global Regulatory Science Leadership Team, Project Development Teams and senior management, as relevant. * Provide input to the end-to-end labeling process. * Ability to lead and manage ...
Deerfield, IL · On-site
$220K - $250K/yr
Ability to lead and work in cross-functional, matrixed, hybrid and multinational teams. * Demonstrated team leadership and motivation of staff to successfully execute global labeling regulatory ...
Deerfield, IL · On-site
$220K - $250K/yr
Ability to lead and work in cross-functional, matrixed, hybrid and multinational teams. * Demonstrated team leadership and motivation of staff to successfully execute global labeling regulatory ...
Ability to lead and work in cross-functional, matrixed, hybrid and multinational teams. * Demonstrated team leadership and motivation of staff to successfully execute global labeling regulatory ...
Ability to lead and work in cross-functional, matrixed, hybrid and multinational teams. * Demonstrated team leadership and motivation of staff to successfully execute global labeling regulatory ...
Durham, NC · On-site
$129 - $359/hr
... to the Global Regulatory Science Leadership Team, Project Development Teams and senior management, as relevant. * Provide input to the end-to-end labeling process. * Ability to lead and manage ...
New
Durham, NC · On-site
$129 - $359/hr
... to the Global Regulatory Science Leadership Team, Project Development Teams and senior management, as relevant. * Provide input to the end-to-end labeling process. * Ability to lead and manage ...
New
Irvine, CA · On-site
Our Global Operations & Quality team plays a central part in ensuring our products are delivered to ... Lead solution development for labeling projects by recommending activities and solution ...
Irvine, CA · On-site
Our Global Operations & Quality team plays a central part in ensuring our products are delivered to ... Lead solution development for labeling projects by recommending activities and solution ...
Irvine, CA · On-site
Our Global Operations & Quality team plays a central part in ensuring our products are delivered to ... Lead solution development for labeling projects by recommending activities and solution ...
Irvine, CA · On-site
Our Global Operations & Quality team plays a central part in ensuring our products are delivered to ... Lead solution development for labeling projects by recommending activities and solution ...
Ability to lead and work in cross-functional, matrixed, hybrid and multinational teams. * Demonstrated team leadership and motivation of staff to successfully execute global labeling regulatory ...
Ability to lead and work in cross-functional, matrixed, hybrid and multinational teams. * Demonstrated team leadership and motivation of staff to successfully execute global labeling regulatory ...
Ability to lead and work in cross-functional, matrixed, hybrid and multinational teams. * Demonstrated team leadership and motivation of staff to successfully execute global labeling regulatory ...
Ability to lead and work in cross-functional, matrixed, hybrid and multinational teams. * Demonstrated team leadership and motivation of staff to successfully execute global labeling regulatory ...
Durham, NC · On-site
$128K - $358K/yr
... to the Global Regulatory Science Leadership Team, Project Development Teams and senior management, as relevant. * Provide input to the end-to-end labeling process. * Ability to lead and manage ...
Durham, NC · On-site
$128K - $358K/yr
... to the Global Regulatory Science Leadership Team, Project Development Teams and senior management, as relevant. * Provide input to the end-to-end labeling process. * Ability to lead and manage ...
$128K - $358K/yr
... to the Global Regulatory Science Leadership Team, Project Development Teams and senior management, as relevant. * Provide input to the end-to-end labeling process. * Ability to lead and manage ...
$128K - $358K/yr
... to the Global Regulatory Science Leadership Team, Project Development Teams and senior management, as relevant. * Provide input to the end-to-end labeling process. * Ability to lead and manage ...
Boston, MA · On-site +1
$185K - $278K/yr
The Regulatory Labeling Director will lead the strategic development of global labeling on one or more marketed products. This role will be responsible for the development and maintenance of global ...
Boston, MA · On-site +1
$185K - $278K/yr
The Regulatory Labeling Director will lead the strategic development of global labeling on one or more marketed products. This role will be responsible for the development and maintenance of global ...
... the global labelling and promotional strategy. * Support the GRDRA Therapeutic Areas cross ... Lead the regulatory review of promotional materials related to marketed products disease state ...
... the global labelling and promotional strategy. * Support the GRDRA Therapeutic Areas cross ... Lead the regulatory review of promotional materials related to marketed products disease state ...
Boston, MA · Hybrid
$185K - $278K/yr
The Regulatory Labeling Director will lead the strategic development of global labeling on one or more marketed products. This role will be responsible for the development and maintenance of global ...
Boston, MA · Hybrid
$185K - $278K/yr
The Regulatory Labeling Director will lead the strategic development of global labeling on one or more marketed products. This role will be responsible for the development and maintenance of global ...
... the global labelling and promotional strategy. * Support the GRDRA Therapeutic Areas cross ... Lead the regulatory review of promotional materials related to marketed products disease state ...
... the global labelling and promotional strategy. * Support the GRDRA Therapeutic Areas cross ... Lead the regulatory review of promotional materials related to marketed products disease state ...
New York, NY · On-site
$35/hr
Company Description Global Channel Management is a technology company that specializes in various ... Labeling Team Lead, or to a Senior Manager in International Labeling Group. This position may ...
New York, NY · On-site
$35/hr
Company Description Global Channel Management is a technology company that specializes in various ... Labeling Team Lead, or to a Senior Manager in International Labeling Group. This position may ...
Los Angeles, CA · On-site
$161K - $213K/yr
The Position The Director of Regulatory Affairs is Arrowhead's Labeling lead, who drives cross-functional development and execution of global regulatory labeling strategy. This individual will manage ...
Quick apply
Los Angeles, CA · On-site
$161K - $213K/yr
The Position The Director of Regulatory Affairs is Arrowhead's Labeling lead, who drives cross-functional development and execution of global regulatory labeling strategy. This individual will manage ...
Pasadena, CA · On-site
$163K - $216K/yr
The Position The Director of Regulatory Affairs is Arrowhead's Labeling lead, who drives cross-functional development and execution of global regulatory labeling strategy. This individual will manage ...
Pasadena, CA · On-site
$163K - $216K/yr
The Position The Director of Regulatory Affairs is Arrowhead's Labeling lead, who drives cross-functional development and execution of global regulatory labeling strategy. This individual will manage ...
NJ · On-site
Global Labeling Strategist Work Location - Remote Global Labeling Strategist has overall ... Ability to influence and lead a diverse group of Subject Matter Experts from a variety of ...
Quick apply
NJ · On-site
Global Labeling Strategist Work Location - Remote Global Labeling Strategist has overall ... Ability to influence and lead a diverse group of Subject Matter Experts from a variety of ...
$159K - $210K/yr
The Position The Director of Regulatory Affairs is Arrowhead's Labeling lead, who drives cross-functional development and execution of global regulatory labeling strategy. This individual will manage ...
Quick apply
$159K - $210K/yr
The Position The Director of Regulatory Affairs is Arrowhead's Labeling lead, who drives cross-functional development and execution of global regulatory labeling strategy. This individual will manage ...
| Aspect | Internship Global Labeling Lead | Global Labeling Associate |
|---|---|---|
| Required Credentials | Currently pursuing or recently completed a degree in life sciences or related field | Typically entry-level, with some background in life sciences or related area |
| Work Environment | Internship setting within pharmaceutical or biotech companies, focusing on labeling projects | Support role in labeling teams, assisting with documentation and compliance tasks |
| Employer & Industry Usage | Used in pharmaceutical companies during internship programs for future labeling professionals | Commonly employed as entry-level support staff in labeling departments |
The Internship Global Labeling Lead is an internship position aimed at gaining experience in global labeling processes, often involving project support and learning. In contrast, the Global Labeling Associate is an entry-level role focused on assisting with labeling documentation and compliance tasks. The internship is temporary and educational, while the associate role is a foundational position within the labeling team, often leading to further career development.
Full-time
Medical, Dental, Vision, Life, Retirement, PTO
Posted 23 days ago
7.9
Based on 176 frontline employees who took The Breakroom Quiz
160th of 538 rated manufacturers
Careers that change lives start here. Medtronic is a global leader in healthcare technology with a Mission to alleviate pain, restore health, and extend life. Our 95,000 employees work across more than 150 countries to put patients first - developing innovative medical technologies that improve the lives of 72+ million patients each year. Your unique talents will help shape the future of healthcare while building a career grounded in purpose, growth, and impact.
A Day in the LifeThe Labeling Specialist drives the development, execution, and continuous improvement of product labeling to support successful product launches, regulatory compliance, and operational excellence. This role partners closely with Packaging Engineering, Product Development, Manufacturing, Regulatory Affairs, Quality, and global stakeholders to deliver accurate, compliant, and market-ready labeling solutions.Responsibilities may include the following and other duties may be assigned.
Lead the creation, review, approval, and release of labeling components that support new product development and commercialized products.
Drive development of labeling design inputs, content specifications, and final label artwork to ensure alignment with product, regulatory, and business requirements.
Manage labeling project timelines, proactively identify risks, and ensure on-time delivery of labeling milestones.
Collaborate cross-functionally with Engineering, Regulatory Affairs, Manufacturing, and Quality teams to resolve labeling challenges and accelerate project execution.
Review and approve package labeling to ensure compliance with documented design requirements, applicable regulations, and internal standards.
Identify and implement process, system, and workflow improvements that enhance labeling quality, efficiency, and scalability.
Coordinate and oversee translation activities for global labeling to support international product registrations and market launches.
Maintain and optimize labeling data within enterprise labeling systems and databases, ensuring accuracy, consistency, and traceability.
Create, edit, and validate labeling content for medical devices and related products while maintaining the highest standards of accuracy and compliance.
Ensure labeling artwork, proofs, and production deliverables meet regulatory, legal, quality, and corporate branding requirements.
Monitor evolving domestic and international labeling regulations and proactively incorporate changes into labeling processes.
Evaluate promotional and commercial materials to ensure consistency with approved product claims and supporting data.
Champion continuous improvement initiatives by assessing labeling processes, tools, systems, and policies and driving innovative solutions.
Required Knowledge and Experience:Requires a Bachelor's degree and minimum of 2 years of relevant experience, or advanced degree with 0 years of experience.
Preferred Qualifications
Demonstrated success managing labeling or packaging projects within a regulated industry environment.
Ability to quickly learn, adopt, and optimize new digital tools, labeling systems, and emerging technologies, including AI-enabled solutions.
Strong attention to detail with a proven ability to identify risks and ensure data accuracy and compliance.
Advanced proficiency with Microsoft Office applications, particularly Excel, and experience utilizing business systems to support operational processes.
Experience collaborating with global, cross-functional teams to achieve project objectives and business outcomes.
Proven knowledge of medical device labeling regulations, standards, and global compliance requirements.
Experience developing, reviewing, and approving product labeling within highly regulated environments.
Proficiency with Adobe Illustrator or other graphic design and labeling software tools.
Strong proofreading, editing, and content management skills with exceptional focus on quality and accuracy.
Experience working in Agile environments, contributing to continuous improvement and accelerated project delivery.
Ability to leverage data analytics, automation, and AI tools to improve labeling efficiency, accuracy, and compliance.
For Baccalaureate degrees earned outside of the United States, a degree that satisfies the requirements of 8 C.F.R. 214.2(h)(4)(iii)(A) is required.
Physical Job Requirements
The above statements are intended to describe the general nature and level of work being performed by employees assigned to this position, but they are not an exhaustive list of all the required responsibilities and skills of this position.
The physical demands described within the Responsibilities section of this job description are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. For Office Roles: While performing the duties of this job, the employee is regularly required to be independently mobile. The employee is also required to interact with a computer, and communicate with peers and co-workers. Contact your manager or local HR to understand the Work Conditions and Physical requirements that may be specific to each role.
U.S. Work Authorization & Sponsorship
At Medtronic, we are committed to fostering an environment where employees can thrive and make a meaningful impact. In alignment with our enterprise-wide workforce planning approach, U.S. work authorization sponsorship (H-1B, TN, J, etc.) is offered exclusively for Principal-level roles and above, where specialized expertise aligns with long-term business needs. Roles below the Principal level require candidates to possess unrestricted U.S. work authorization at the time of hire and for the duration of employment.
Recruitment Fraud Alert
We are aware of phishing scams targeting job seekers. Please keep the following in mind:
Apply only through official Medtronic channels. All legitimate Medtronic recruiting communications come from approved Medtronic platforms and official @medtronic.com email addresses.
Medtronic will never ask for payment or sensitive personal information (such as bank account or Social Security details) during early stages of the hiring process. Any such requests are not legitimate.
If you receive a suspicious message claiming to be from Medtronic, do not respond, click links, or open attachments.
If you have any questions, concerns regarding the authenticity of a communication alleged to have been made by or on behalf of Medtronic, please contact us immediately at AskHR@medtronic.com.
Benefits & CompensationMedtronic offers a competitive Salary and flexible Benefits Package
A commitment to our employees lives at the core of our values. We recognize their contributions. They share in the success they help to create. We offer a wide range of benefits, resources, and competitive compensation plans designed to support you at every career and life stage.
The following benefits and additional compensation are available to those regular employees who work 20+ hours per week: Health, Dental and vision insurance,Health Savings Account,Healthcare Flexible Spending Account,Life insurance, Long-term disability leave,Dependent daycare spending account,Tuition assistance/reimbursement, andSimple Steps (global well-being program).
The following benefits and additional compensation are available to all regular employees:Incentive plans, 401(k) plan plus employer contribution and match,Short-term disability,Paid time off,Paid holidays,Employee Stock Purchase Plan,Employee Assistance Program,Non-qualified Retirement Plan Supplement (subject to IRS earning minimums), andCapital Accumulation Plan (available to Vice Presidents and above, or subject to IRS earning minimums).
Regular employees are those who are not temporary, such as interns. Temporary employees are eligible for paid sick time, as required under applicable state law, and the Employee Stock Purchase Plan. Please note some of the above benefits may not apply to workers in Puerto Rico.
Further details are available at the link below:
Medtronic benefits and compensation plans
It is the policy of Medtronic to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by federal, state or local law. In addition, Medtronic will provide reasonable accommodations for qualified individuals with disabilities.
If you are applying to perform work for Medtronic, Inc. ("Medtronic") in any position which will involve performing at least two (2) hours of work on average each week within the unincorporated areas of Los Angeles County, you can findhere a list of all material job duties of the specific job position which Medtronic reasonably believes that criminal history may have a direct, adverse and negative relationship potentially resulting in the withdrawal of a conditional offer of employment. Medtronic will consider for employment qualified job applicants with arrest or conviction records in accordance with the Los Angeles County Fair Chance Ordinance for Employers and the California Fair Chance Act.
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