Label Designer
Vernon Hills, IL · On-site
... as a Labeling Designer? *** How much experience in years do you have with technical data entry? *** How much experience in years do you have with medical device labels? *** How much experience in ...
New
Vernon Hills, IL · On-site
... as a Labeling Designer? *** How much experience in years do you have with technical data entry? *** How much experience in years do you have with medical device labels? *** How much experience in ...
New
Vernon Hills, IL · On-site
... as a Labeling Designer? *** How much experience in years do you have with technical data entry? *** How much experience in years do you have with medical device labels? *** How much experience in ...
New
Chicago, IL · On-site
... as a Labeling Designer? *** How much experience in years do you have with technical data entry? *** How much experience in years do you have with medical device labels? *** How much experience in ...
New
Chicago, IL · On-site
... as a Labeling Designer? *** How much experience in years do you have with technical data entry? *** How much experience in years do you have with medical device labels? *** How much experience in ...
New
Carol Stream, IL · On-site
... as a Labeling Designer? *** How much experience in years do you have with technical data entry? *** How much experience in years do you have with medical device labels? *** How much experience in ...
New
Carol Stream, IL · On-site
... as a Labeling Designer? *** How much experience in years do you have with technical data entry? *** How much experience in years do you have with medical device labels? *** How much experience in ...
New
Northfield, IL · On-site
$67K - $101K/yr
Minimum of two (2) years of working experience and current knowledge of medical device labeling/UDI regulations, standards, and guidance Knowledge/Skills/Abilities: Work experience in evaluating ...
Northfield, IL · On-site
$67K - $101K/yr
Minimum of two (2) years of working experience and current knowledge of medical device labeling/UDI regulations, standards, and guidance Knowledge/Skills/Abilities: Work experience in evaluating ...
Northfield, IL · On-site
$67K - $101K/yr
Minimum of two (2) years of working experience and current knowledge of medical device labeling/UDI regulations, standards, and guidance Knowledge/Skills/Abilities: Work experience in evaluating ...
Northfield, IL · On-site
$67K - $101K/yr
Minimum of two (2) years of working experience and current knowledge of medical device labeling/UDI regulations, standards, and guidance Knowledge/Skills/Abilities: Work experience in evaluating ...
Northfield, IL · On-site
$67K - $101K/yr
Minimum of two (2) years of working experience and current knowledge of medical device labeling/UDI regulations, standards, and guidance Knowledge/Skills/Abilities: Work experience in evaluating ...
Northfield, IL · On-site
$67K - $101K/yr
Minimum of two (2) years of working experience and current knowledge of medical device labeling/UDI regulations, standards, and guidance Knowledge/Skills/Abilities: Work experience in evaluating ...
Northfield, IL · On-site
$67K - $101K/yr
Minimum of two (2) years of working experience and current knowledge of medical device labeling/UDI regulations, standards, and guidance Knowledge/Skills/Abilities: Work experience in evaluating ...
Northfield, IL · On-site
$67K - $101K/yr
Minimum of two (2) years of working experience and current knowledge of medical device labeling/UDI regulations, standards, and guidance Knowledge/Skills/Abilities: Work experience in evaluating ...
... Medical Device (SaMD), CE Marking, labeling requirements, adverse event reporting, field corrective actions, Declaration of Conformity, Buy American Act (BAA), Build America Buy America Act (BABAA ...
New
... Medical Device (SaMD), CE Marking, labeling requirements, adverse event reporting, field corrective actions, Declaration of Conformity, Buy American Act (BAA), Build America Buy America Act (BABAA ...
New
... Device Identifier GUDID maintenance, on market labeling and submission impact reviews, labeling reviews and adverse event reporting; Yearly Registration of US FDA Establishment License and updates to ...
... Device Identifier GUDID maintenance, on market labeling and submission impact reviews, labeling reviews and adverse event reporting; Yearly Registration of US FDA Establishment License and updates to ...
Assess incoming documentation, including clinical forms and medical information, for complaint data ... labeling. Evaluate internal and external lab analysis. Coordinate with inter- and intra ...
Assess incoming documentation, including clinical forms and medical information, for complaint data ... labeling. Evaluate internal and external lab analysis. Coordinate with inter- and intra ...
Class I Medical Device regulations * Product labeling and claims compliance * cGMP requirements * Preferred Qualifications: * Advanced degree in scientific discipline, regulatory affairs, or related ...
Class I Medical Device regulations * Product labeling and claims compliance * cGMP requirements * Preferred Qualifications: * Advanced degree in scientific discipline, regulatory affairs, or related ...
Niles, IL · On-site
Class I Medical Device regulations * Product labeling and claims compliance * cGMP requirements * Preferred Qualifications: * Advanced degree in scientific discipline, regulatory affairs, or related ...
Niles, IL · On-site
Class I Medical Device regulations * Product labeling and claims compliance * cGMP requirements * Preferred Qualifications: * Advanced degree in scientific discipline, regulatory affairs, or related ...
North Chicago, IL · On-site
Support quality functions including Document Control, Device QA, Labeling, Validation, Training ... Experience working in pharmaceutical or medical device manufacturing environments. I am actively ...
Quick apply
North Chicago, IL · On-site
Support quality functions including Document Control, Device QA, Labeling, Validation, Training ... Experience working in pharmaceutical or medical device manufacturing environments. I am actively ...
Lake Forest, IL · On-site
Create structured product labeling for FDA submission Qualifications * Adobe Acrobat * MS Word * Medical Device industry Additional Information All your information will be kept confidential ...
Lake Forest, IL · On-site
Create structured product labeling for FDA submission Qualifications * Adobe Acrobat * MS Word * Medical Device industry Additional Information All your information will be kept confidential ...
Medical Device Manufacturing Position: Product Development Engineering Tech Duration: 10+ months ... This would include receiving in, staging, labeling, tracking and prepping test product, trialing ...
Quick apply
Medical Device Manufacturing Position: Product Development Engineering Tech Duration: 10+ months ... This would include receiving in, staging, labeling, tracking and prepping test product, trialing ...
Providing compliance and regulatory advisory services for pharmaceutical, medical device and other ... Regulatory/Medical/Legal promotional review and labeling services leadership and roadmap ...
Providing compliance and regulatory advisory services for pharmaceutical, medical device and other ... Regulatory/Medical/Legal promotional review and labeling services leadership and roadmap ...
Support processes for Medical Device Reporting and Complaints for Avalign as specification ... Advise project teams on subjects such as premarket regulatory requirements, export and labeling ...
Support processes for Medical Device Reporting and Complaints for Avalign as specification ... Advise project teams on subjects such as premarket regulatory requirements, export and labeling ...
Schaumburg, IL · On-site
$75 - $95/hr
Support processes for Medical Device Reporting and Complaints for Avalign as specification ... Advise project teams on subjects such as premarket regulatory requirements, export and labeling ...
Schaumburg, IL · On-site
$75 - $95/hr
Support processes for Medical Device Reporting and Complaints for Avalign as specification ... Advise project teams on subjects such as premarket regulatory requirements, export and labeling ...
Deerfield, IL · On-site
$220K - $250K/yr
Supports Lundbeck Product Labeling Committee activities as LPLC reviewer, coordinating and ... medical device and/or biotech industry, with 7+ years of experience in Regulatory Affairs. * 5+ ...
Deerfield, IL · On-site
$220K - $250K/yr
Supports Lundbeck Product Labeling Committee activities as LPLC reviewer, coordinating and ... medical device and/or biotech industry, with 7+ years of experience in Regulatory Affairs. * 5+ ...
Supports Lundbeck Product Labeling Committee activities as LPLC reviewer, coordinating and ... medical device and/or biotech industry, with 7+ years of experience in Regulatory Affairs. * 5+ ...
Supports Lundbeck Product Labeling Committee activities as LPLC reviewer, coordinating and ... medical device and/or biotech industry, with 7+ years of experience in Regulatory Affairs. * 5+ ...
$16.30 is the 25th percentile. Wages below this are outliers.
$13.37 - $21.09
66% of jobs
$21.09 - $28.82
6% of jobs
$32.03 is the 75th percentile. Wages above this are outliers.
$28.82 - $36.54
6% of jobs
$36.54 - $44.26
7% of jobs
$44.26 - $51.98
5% of jobs
$51.98 - $59.70
5% of jobs
$59.70 - $67.42
1% of jobs
$67.42 - $75.15
0% of jobs
$75.15 - $82.87
0% of jobs
$82.87 - $90.59
1% of jobs
$90.59 - $98.31
1% of jobs
$13
$31
$98
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.
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.
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.
For Medical Device Labeling jobs in Chicago, IL, the most frequently searched job titles are:
The top searched job categories for Medical Device Labeling jobs in Chicago, IL are:

Our client, based in Vernon Hills, IL, is looking to hire a Labeling Designer Consultant.
Project duration: 6 months with the potential to convert over to a full time permanent role
I have listed below a detailed job description for your review.
If you have the required experience and interest, please email me a current resume, along with your responses to the following questions:
*** How much experience in years do you have as a Labeling Designer?
*** How much experience in years do you have with technical data entry?
*** How much experience in years do you have with medical device labels?
*** How much experience in years do you have with Excel, Word, Outlook & PowerPoint?
*** How much experience in years do you have with Adobe Illustrator?
*** How much experience in years do you have with databases?
*** Do you hold a Bachelor s degree? If yes, what was your major?
*** What industry certifications do you hold?
*** What is your desired hourly rate?
*** Where do you currently reside (city, state)?
*** Are you able to work in Vernon Hills, IL?
*** What is your availability to start a new project?
Thank you!
Steven Edelman
Pivotal Solutions, Inc.
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Summary:Responsible for supporting company s finished goods labeling development processes. Assists in all activities necessaryto develop, configure, generate, revise and assure the integrity of product labeling (Global Labeling System generated labels using templates and database for labeling content, label artwork, package artwork, IFUs, image files, etc.), domestic and foreign, for products manufactured at company or products manufactured for company at Contract Manufacturing sites, vendors and suppliers.
These duties include, but are not limited to the following: Parses and loads label content into labeling systems; collaborates with project teams; reviews, corrects and approves content and configurations within the labeling system; makes judgments on designs, controls and maintains global label templates, while seeking consensus from the team to ensure consistent corporate identity; manages the global format database; manages labeling approval workflows (creation, review, approval, and release); performs visual label verification to review labeling manually and within labeling systems to confirm indicated labeling content, elements, formatting and configuration is accurate and indicated per company standards; provides troubleshooting support to manufacturing, distribution and third-party locations.
Responsibilities:Note: This is not an exhaustive list of duties or functions and may not comprise of all 'essential functions' necessary to perform this role. (for ADA purposes)
Essential Functions of the Role:o Adobe Illustrator and ability to use various databases is a plus.