Ensure adherence to global medical device labeling, packaging, and design control requirements * Execution & Delivery: Ensure on-time, high-quality delivery of labeling and packaging across NPD and ...
Ensure adherence to global medical device labeling, packaging, and design control requirements * Execution & Delivery: Ensure on-time, high-quality delivery of labeling and packaging across NPD and ...
Principal Regulatory Affairs Specialist - Bracco Medical Technologies
Eden Prairie, MN · On-site
$131 - $143/hr
Review device labeling, advertising, and promotional materials for compliance with approved ... Bracco Medical Technologies also offers a comprehensive total rewards package, including health ...
Principal Regulatory Affairs Specialist - Bracco Medical Technologies
Eden Prairie, MN · On-site
$131 - $143/hr
Review device labeling, advertising, and promotional materials for compliance with approved ... Bracco Medical Technologies also offers a comprehensive total rewards package, including health ...
Medical Device Assembler, Operations - Shift 1
Dublin, OH · On-site
$16/hr
Job Title: Medical Device Assembler Duration: 12 Months Location: Dublin OH 43016 * Able to ... Weigh count, package, and label finished product. Education and Experience: * High School Diploma ...
Quick apply
Medical Device Assembler, Operations - Shift 1
Dublin, OH · On-site
$16/hr
Job Title: Medical Device Assembler Duration: 12 Months Location: Dublin OH 43016 * Able to ... Weigh count, package, and label finished product. Education and Experience: * High School Diploma ...
Medical Device Quality Inspector
Madison, WI · On-site
$55 - $85/hr
Ensures storage and handling of product and labeling in a controlled and secure manner. * Supports ... Knowledge of FDA Quality System Regulations and ISO13485 pertaining to medical device manufacturing ...
Medical Device Quality Inspector
Madison, WI · On-site
$55 - $85/hr
Ensures storage and handling of product and labeling in a controlled and secure manner. * Supports ... Knowledge of FDA Quality System Regulations and ISO13485 pertaining to medical device manufacturing ...
... and labeling--to support IDE, PMA, and other international filings. An ideal candidate brings strong writing and analytical skills, a solid understanding of medical device regulations, and the ...
Quick apply
... and labeling--to support IDE, PMA, and other international filings. An ideal candidate brings strong writing and analytical skills, a solid understanding of medical device regulations, and the ...
Medical device labeling experience preferred. * Experience with labeling systems such as Priysm and Loftware/Spectrum preferred. Role Characteristics * Entry-level individual contributor working on a ...
Medical device labeling experience preferred. * Experience with labeling systems such as Priysm and Loftware/Spectrum preferred. Role Characteristics * Entry-level individual contributor working on a ...
Associate Graphic Designer
North Haven, CT · On-site
$28 - $31/hr
Medical device labeling experience preferred. * Experience with labeling systems such as Priysm and Loftware/Spectrum preferred. Role Characteristics * Entry-level individual contributor working on a ...
Quick apply
Associate Graphic Designer
North Haven, CT · On-site
$28 - $31/hr
Medical device labeling experience preferred. * Experience with labeling systems such as Priysm and Loftware/Spectrum preferred. Role Characteristics * Entry-level individual contributor working on a ...
Review device labeling, including all graphic material. Prepare export certificates, medical device listings, annual establishment registrations for submission to the U.S. Food and Drug ...
Quick apply
Review device labeling, including all graphic material. Prepare export certificates, medical device listings, annual establishment registrations for submission to the U.S. Food and Drug ...
Sr. RA Specialist
San Jose, CA · Hybrid
FDA 21 CFR Part 820 and applicable FDA regulations, EU MDR (2017/745), ISO 13485, ISO 14971 Risk Management, MDSAP requirements, Medical device labeling requirements * Regulatory Affairs ...
Sr. RA Specialist
San Jose, CA · Hybrid
FDA 21 CFR Part 820 and applicable FDA regulations, EU MDR (2017/745), ISO 13485, ISO 14971 Risk Management, MDSAP requirements, Medical device labeling requirements * Regulatory Affairs ...
Human Factors Engineer 3, Device Development
Boston, MA · On-site
$101K - $133K/yr
... labeling and secondary packaging) Collaborate with human factors firms (vendors) and manage their ... Experience in human factors engineering and exposure to design and development of medical device ...
Human Factors Engineer 3, Device Development
Boston, MA · On-site
$101K - $133K/yr
... labeling and secondary packaging) Collaborate with human factors firms (vendors) and manage their ... Experience in human factors engineering and exposure to design and development of medical device ...
Human Factors Engineer 3, Device Development
Boston, MA · On-site
$101K - $133K/yr
... device, labeling and secondary packaging) * Collaborate with human factors firms (vendors) and ... Experience in human factors engineering and exposure to design and development of medical device ...
Human Factors Engineer 3, Device Development
Boston, MA · On-site
$101K - $133K/yr
... device, labeling and secondary packaging) * Collaborate with human factors firms (vendors) and ... Experience in human factors engineering and exposure to design and development of medical device ...
Principal Regulatory Affairs Specialist - Bracco Medical Technologies
Eden Prairie, MN · On-site
$131 - $143/hr
Why Join Bracco Medical Technologies? We care as much about our employees as we do our patients ... Review device labeling, advertising, and promotional materials for compliance with approved ...
Principal Regulatory Affairs Specialist - Bracco Medical Technologies
Eden Prairie, MN · On-site
$131 - $143/hr
Why Join Bracco Medical Technologies? We care as much about our employees as we do our patients ... Review device labeling, advertising, and promotional materials for compliance with approved ...
Human Factors Engineer 3, Device Development
Boston, MA · On-site
$101K - $133K/yr
... device, labeling and secondary packaging) * Collaborate with human factors firms (vendors) and ... Experience in human factors engineering and exposure to design and development of medical device ...
Human Factors Engineer 3, Device Development
Boston, MA · On-site
$101K - $133K/yr
... device, labeling and secondary packaging) * Collaborate with human factors firms (vendors) and ... Experience in human factors engineering and exposure to design and development of medical device ...
Human Factors Engineer 3, Device Development
Boston, MA · On-site
$102 - $133/hr
... device, labeling and secondary packaging) * Collaborate with human factors firms (vendors) and ... Experience in human factors engineering and exposure to design and development of medical device ...
Human Factors Engineer 3, Device Development
Boston, MA · On-site
$102 - $133/hr
... device, labeling and secondary packaging) * Collaborate with human factors firms (vendors) and ... Experience in human factors engineering and exposure to design and development of medical device ...
Provides guidance on combination product/drug-device labeling. * Interprets scientific and clinical ... medical affairs, etc.). 5-7 years of direct experience in a global, US, or EU labeling role is ...
Provides guidance on combination product/drug-device labeling. * Interprets scientific and clinical ... medical affairs, etc.). 5-7 years of direct experience in a global, US, or EU labeling role is ...
$102 - $133/hr
... device, labeling and secondary packaging) * Collaborate with human factors firms (vendors) and ... Experience in human factors engineering and exposure to design and development of medical device ...
$102 - $133/hr
... device, labeling and secondary packaging) * Collaborate with human factors firms (vendors) and ... Experience in human factors engineering and exposure to design and development of medical device ...
Human Factors Engineer 3, Device Development
Boston, MA · On-site
$101K - $133K/yr
... device, labeling and secondary packaging) * Collaborate with human factors firms (vendors) and ... Experience in human factors engineering and exposure to design and development of medical device ...
Human Factors Engineer 3, Device Development
Boston, MA · On-site
$101K - $133K/yr
... device, labeling and secondary packaging) * Collaborate with human factors firms (vendors) and ... Experience in human factors engineering and exposure to design and development of medical device ...
Human Factors Engineer 3, Device Development
Boston, MA · On-site
$102 - $133/hr
... device, labeling and secondary packaging) * Collaborate with human factors firms (vendors) and ... Experience in human factors engineering and exposure to design and development of medical device ...
Human Factors Engineer 3, Device Development
Boston, MA · On-site
$102 - $133/hr
... device, labeling and secondary packaging) * Collaborate with human factors firms (vendors) and ... Experience in human factors engineering and exposure to design and development of medical device ...
You will work onsite at our Conroe,Texas campus (Houston area) to design medical device product labels and instructions for use (IFU) documents for our medical device product portfolio. What You'll ...
You will work onsite at our Conroe,Texas campus (Houston area) to design medical device product labels and instructions for use (IFU) documents for our medical device product portfolio. What You'll ...
Principal Regulatory Affairs Specialist - Bracco Medical Technologies
Eden Prairie, MN · On-site
$131K - $143K/yr
Why Join Bracco Medical Technologies? We care as much about our employees as we do our patients ... Review device labeling, advertising, and promotional materials for compliance with approved ...
Principal Regulatory Affairs Specialist - Bracco Medical Technologies
Eden Prairie, MN · On-site
$131K - $143K/yr
Why Join Bracco Medical Technologies? We care as much about our employees as we do our patients ... Review device labeling, advertising, and promotional materials for compliance with approved ...
Medical Device Labeling information
See salary details
$15.82 is the 25th percentile. Wages below this are outliers.
$12.98 - $20.48
66% of jobs
$20.48 - $27.97
6% of jobs
$31.10 is the 75th percentile. Wages above this are outliers.
$27.97 - $35.47
6% of jobs
$35.47 - $42.96
7% of jobs
$42.96 - $50.46
5% of jobs
$50.46 - $57.95
5% of jobs
$57.95 - $65.45
1% of jobs
$65.45 - $72.95
0% of jobs
$72.95 - $80.44
0% of jobs
$80.44 - $87.94
1% of jobs
$87.94 - $95.43
1% of jobs
$12
$30
$95
How much do medical device labeling jobs pay per hour?
What is a medical device labeling?
A Medical Device Labeling job involves creating, reviewing, and managing labeling content for medical devices to ensure compliance with regulatory requirements. This includes instructions for use, packaging labels, and safety information for healthcare professionals and patients. Professionals in this role collaborate with regulatory, quality, and engineering teams to meet industry standards and country-specific regulations. Their work ensures that medical devices are used safely and effectively, reducing risks associated with improper usage.
What does a medical device labeling do?
Professionals in Medical Device Labeling are responsible for creating, reviewing, and updating product labels, instructions for use, and packaging materials to ensure compliance with regulatory standards. They often collaborate closely with regulatory affairs, engineering, and quality assurance teams to gather technical product information and incorporate feedback. Daily activities may also include managing document control processes, implementing labeling changes driven by new regulations or product updates, and preparing submissions for global markets. Attention to detail and the ability to manage multiple projects simultaneously are crucial for success in this role.
What are the key skills and qualifications needed to thrive in medical device labeling?
To thrive in Medical Device Labeling, you need a strong understanding of regulatory requirements (such as FDA and EU MDR), attention to detail, and experience with technical writing or documentation, often supported by a degree in life sciences or a related field. Familiarity with labeling management systems, document control tools, and knowledge of ISO standards are key technical qualifications, and certifications like RAC can be advantageous. Strong communication, collaboration, and organizational skills set candidates apart, as these roles often involve coordinating with cross-functional teams such as regulatory, engineering, and quality assurance. These capabilities ensure labeling materials meet strict compliance standards, avoid costly errors or recalls, and support timely product launch and patient safety.
What cities are hiring for Medical Device Labeling jobs?
Cities with the most Medical Device Labeling job openings:
What are the most commonly searched types of Medical Device Labeling jobs?
The most popular types of Medical Device Labeling jobs are:
What states have the most Medical Device Labeling jobs?
States with the most job openings for Medical Device Labeling jobs include:
What job categories do people searching Medical Device Labeling jobs look for?
The top searched job categories for Medical Device Labeling jobs are:

Full-time
Re-posted yesterday
Key responsibilities
Define and execute the long-term strategy for labeling and packaging aligned with UCC growth objectives
Oversee labeling and packaging deliverables across the full product lifecycle, ensuring alignment with development and commercialization plans
Ensure all labeling and packaging meet global regulatory requirements and maintain compliance within BD's Quality Management System
BD rating
7.3
Based on 143 frontline employees who took The Breakroom Quiz
314th of 499 rated machine equipment manufacturers
Job description
BD is one of the largest global medical technology companies in the world. Advancing the world of health™ is our Purpose, and it's no small feat. It takes the imagination and passion of all of us-from design and engineering to the manufacturing and marketing of our billions of MedTech products per year-to look at the impossible and find transformative solutions that turn dreams into possibilities.
Job Description
Director, Labeling & Packaging, R&D - UCC
Be part of something bigger!
BD is one of the largest global medical technology companies in the world and is advancing the world of health by improving medical discovery, diagnostics, and the delivery of care. With over 70,000 employees worldwide, BD addresses some of the most complex global health challenges through innovation, quality, and operational excellence.
Position Summary
The Director of Labeling & Packaging is a key member of the UCC R&D leadership team, responsible for setting the strategic direction and operational execution of labeling and packaging across innovation, new product development (NPD), and sustaining engineering (SE).
This role brings a consumer-centric mindset to product experience-ensuring that labeling and packaging not only meet regulatory requirements but also enhance usability, clarity, and market competitiveness. The Director will drive process excellence, efficiency, and scalability within the labeling and packaging functions while ensuring compliance with global medical device regulations.
Focus Areas
- Consumer-Centric Design Excellence: Embed consumer product packaging principles to elevate usability, clarity, and shelf/point-of-use impact
- Operational Efficiency & Process Transformation: Drive standardization, automation, and continuous improvement (e.g., AI-enabled workflows, labeling throughput optimization)
- Regulatory Compliance & Quality: Ensure adherence to global medical device labeling, packaging, and design control requirements
- Execution & Delivery: Ensure on-time, high-quality delivery of labeling and packaging across NPD and SE portfolios
- Talent & Organization Development: Build a high-performing, scalable organization with strong technical and operational capabilities
Primary Responsibilities
Strategy & Leadership
- Define and execute the long-term strategy for labeling and packaging aligned with UCC growth objectives
- Serve as the functional leader across labeling and packaging, providing direction across platforms and projects
- Act as a key contributor to functional and business strategy development
Consumer-Centric Packaging & Labeling
- Apply consumer product design principles to improve product differentiation, usability, and customer experience
- Partner with Marketing and Design teams to ensure packaging and labeling meet evolving customer needs and expectations
- Drive innovation in packaging formats, materials, and labeling presentation
Process Excellence & Continuous Improvement
- Lead transformation initiatives to improve labeling and packaging efficiency, throughput, and predictability
- Standardize workflows (e.g., artwork creation, review cycles, release processes) and eliminate waste
- Implement digital and AI-enabled solutions to accelerate labeling and packaging processes
- Develop and track key performance metrics (cycle time, quality, cost, delivery)
Program Execution
- Oversee labeling and packaging deliverables across the full product lifecycle (concept through commercialization and sustaining)
- Ensure alignment with BD's Global Product Development System (GPDS) and design control practices
- Provide governance, risk management, and escalation support for critical programs
Regulatory & Quality Compliance
- Ensure all labeling and packaging meet global regulatory requirements (e.g., FDA, EU MDR, ISO standards)
- Partner with Quality and Regulatory Affairs to ensure compliance within BD's Quality Management System
- Maintain inspection readiness and support audits
Cross-Functional Collaboration
- Partner with R&D, Quality, Regulatory, Operations, Marketing, and Supply Chain
- Ensure seamless integration of labeling and packaging into product development and commercialization plans
- Serve as a key stakeholder in platform and portfolio decision-making
Talent Development & Organization Leadership
- Build and lead a high-performing team of labeling and packaging professionals
- Develop technical depth and leadership capability across the organization
- Drive a culture of accountability, continuous improvement, and BD Excellence mindset
Candidate Profile
BD is seeking a transformational and execution-focused leader who combines consumer product insight with strong operational discipline and regulatory awareness.
Required Qualifications
- Bachelor's degree in engineering, Packaging Science, Industrial Design, or related field (advanced degree preferred)
- 12+ years of experience in packaging, labeling, or product development, including leadership roles
- Proven experience in consumer products packaging and/or industrial design
- Demonstrated success driving process improvements and operational efficiency in a complex organization
- Experience working within regulated industries (medical device preferred)
Preferred Qualifications
- Experience integrating consumer design principles into healthcare or regulated environments
- Knowledge of global labeling and packaging regulations (e.g., FDA, EU MDR, ISO 13485)
- Experience with digital/AI tools for labeling workflows and artwork management
- Background in high-volume consumables or disposable product categories
Critical Skills & Competencies
- Strategic thinking and business acumen
- Strong execution discipline and process mindset
- Consumer mindset and design sensitivity
- Cross-functional leadership and influence
- Data-driven decision making
- Change leadership and organizational transformation
- Talent development and team building
Why Join Us?
Join a leadership team driving a transformation in how UCC delivers innovation-expanding from traditional MedTech into consumer-focused, design-driven solutions at scale.
Here is a BD-style "Key Success Metrics" section you can append to the job description. I've aligned these to your operating model (velocity, capacity, range), labeling/process transformation priorities, and the execution discipline reflected in your internal materials (e.g., focus on delivery, process improvement, and compliance rigor).
Key Success Metrics
Execution & Delivery (Velocity)
- On-Time Labeling & Packaging Delivery: ≥95% of NPD and SE milestones met on time
- Cycle Time Reduction: 20-30% reduction in end-to-end labeling/artwork release cycle time
- Right-First-Time Yield: ≥98% approval rate on first submission for labeling and packaging deliverables
- Launch Readiness: Zero delays to commercialization attributable to labeling or packaging readiness
Operational Efficiency & Capacity
- Throughput Improvement: ≥25% increase in labeling project throughput without proportional headcount increase
- Workload Balance & Utilization: Optimized resource utilization across labeling and packaging teams (measured via load vs. capacity dashboards)
- Automation Adoption: Measurable increase in use of digital/AI-enabled workflows (e.g., artwork comparison, automation of updates)
- Cost Efficiency: Year-over-year reduction in cost per labeling/packaging deliverable
Quality & Compliance
- Audit Performance: Zero major findings related to labeling/packaging in internal/external audits
- Regulatory Compliance: 100% adherence to applicable global regulations (e.g., FDA, EU MDR, ISO 13485)
- Error Rate Reduction: Continuous reduction in labeling errors, deviations, and post-release corrections
- Inspection Readiness: Sustained state of readiness with no compliance-driven business disruption
Consumer-Centric Impact (Range / Market Impact)
- Customer Experience Improvement: Measurable improvements in usability, readability, and product interaction feedback (VOC / HF metrics)
- Design Differentiation: Increased adoption of consumer-driven packaging and labeling innovations across NPD portfolio
- Market Readiness: Packaging and labeling enable clear product positioning and support successful product launches in global markets
Process Excellence & Transformation
- Standardization: Implementation of standardized labeling and packaging workflows across 90%+ of projects
- Continuous Improvement Pipeline: Delivery of targeted Kaizen/CI initiatives with quantified benefits (cycle time, quality, cost)
- Digital Maturity: Advancement of labeling and packaging processes along the digital maturity curve (tools, data, automation)
Talent & Organization
- Team Engagement & Retention: ≥95% retention of key talent and strong engagement scores
- Capability Building: Increased bench strength in consumer packaging, regulatory knowledge, and process excellence
- Leadership Effectiveness: Demonstrated development of high-performing teams and successors
Executive "So What" (optional framing for req justification)
This role is successful when labeling and packaging evolve from a constraint to a competitive advantage-enabling faster launches, improved consumer experience, and scalable global execution without compromising compliance.
Why Join Us?
To find purpose in the possibilities, we need people who can see the bigger picture, who understand the human story that underpins everything we do. We welcome people with the imagination and drive to help us reinvent the future of healthcare. At BD, you'll discover a culture in which you can learn, grow and thrive.
We believe that when people connect in person, we learn faster, collaborate more deeply, and build a stronger culture. Join us and enjoy a culture where face-to-face collaboration supports your learning, your progress, and your success.
To learn more about BD visit https://bd.com/careers.
Becton, Dickinson, and Company is an Equal Opportunity Employer. We evaluate applicants without regard to race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, and other legally protected characteristics.
Required Skills
Optional Skills
Primary Work Location
USA GA - Covington BMD
Additional Locations
Work Shift
About BD
Sourced by ZipRecruiter
BD is one of the largest global medical technology companies in the world and is advancing the world of health by improving medical discovery, diagnostics and the delivery of care. We have over 65,000 employees and a presence in virtually every country around the world to address some of the most challenging global health issues.
Industry
Medical equipment and supplies manufacturing and manufacturing
Company size
10,000+ Employees
Headquarters location
Franklin Lakes, NJ, US