Northfield, IL · Hybrid
$62K - $93K/yr
Job Summary Medline Industries has an immediate opening for an Associate Regulatory Labeling ... Knowledge / Skills / Abilities - Basic knowledge and understanding of FDA product codes and product ...
Northfield, IL · Hybrid
$62K - $93K/yr
Job Summary Medline Industries has an immediate opening for an Associate Regulatory Labeling ... Knowledge / Skills / Abilities - Basic knowledge and understanding of FDA product codes and product ...
Essential Role Functions · Review, verify, and update product labels to ensure compliance with FDA 21 CFR, USDA, U.S. state laws, and applicable requirements for imported foods across a large and ...
Essential Role Functions · Review, verify, and update product labels to ensure compliance with FDA 21 CFR, USDA, U.S. state laws, and applicable requirements for imported foods across a large and ...
$75K - $90K/yr
Working knowledge of food safety and regulatory frameworks (HACCP, FSMA, SQF, USDA/FDA labeling requirements). * ServSafe or equivalent food handler certification required; HACCP certification a plus.
$75K - $90K/yr
Working knowledge of food safety and regulatory frameworks (HACCP, FSMA, SQF, USDA/FDA labeling requirements). * ServSafe or equivalent food handler certification required; HACCP certification a plus.
Berkeley, IL · On-site
$75K - $90K/yr
Working knowledge of food safety and regulatory frameworks (HACCP, FSMA, SQF, USDA/FDA labeling requirements). * ServSafe or equivalent food handler certification required; HACCP certification a plus.
Berkeley, IL · On-site
$75K - $90K/yr
Working knowledge of food safety and regulatory frameworks (HACCP, FSMA, SQF, USDA/FDA labeling requirements). * ServSafe or equivalent food handler certification required; HACCP certification a plus.
$75K - $90K/yr
Working knowledge of food safety and regulatory frameworks (HACCP, FSMA, SQF, USDA/FDA labeling requirements). * ServSafe or equivalent food handler certification required; HACCP certification a plus.
$75K - $90K/yr
Working knowledge of food safety and regulatory frameworks (HACCP, FSMA, SQF, USDA/FDA labeling requirements). * ServSafe or equivalent food handler certification required; HACCP certification a plus.
Romeoville, IL · On-site
$21/hr
Labeling and assist in the preparation and / or assembly of packaging materials including sleeving ... Follow all manufacturing procedures per GMP and FDA requirements. Your Profile / Qualifications
Romeoville, IL · On-site
$21/hr
Labeling and assist in the preparation and / or assembly of packaging materials including sleeving ... Follow all manufacturing procedures per GMP and FDA requirements. Your Profile / Qualifications
Ensure labeling complies with applicable FDA regulations and industry standards. Regulatory Documentation & Submissions * Prepare and maintain regulatory documentation and compliance records.
Ensure labeling complies with applicable FDA regulations and industry standards. Regulatory Documentation & Submissions * Prepare and maintain regulatory documentation and compliance records.
Niles, IL · On-site
Ensure labeling complies with applicable FDA regulations and industry standards. Regulatory Documentation & Submissions * Prepare and maintain regulatory documentation and compliance records.
Niles, IL · On-site
Ensure labeling complies with applicable FDA regulations and industry standards. Regulatory Documentation & Submissions * Prepare and maintain regulatory documentation and compliance records.
Romeoville, IL · On-site
$19 - $21/hr
Labeling and assist in the preparation and / or assembly of packaging materials including sleeving ... Follow all manufacturing procedures per GMP and FDA requirements. Your Profile / Qualifications
Romeoville, IL · On-site
$19 - $21/hr
Labeling and assist in the preparation and / or assembly of packaging materials including sleeving ... Follow all manufacturing procedures per GMP and FDA requirements. Your Profile / Qualifications
Create structured product labeling for FDA submission Qualifications * Adobe Acrobat * MS Word * Medical Device industry Additional Information All your information will be kept confidential ...
Create structured product labeling for FDA submission Qualifications * Adobe Acrobat * MS Word * Medical Device industry Additional Information All your information will be kept confidential ...
... labeling reviews and adverse event reporting; Yearly Registration of US FDA Establishment License and updates to product listings; Export documentation to support shipping. Essential Job Functions:
... labeling reviews and adverse event reporting; Yearly Registration of US FDA Establishment License and updates to product listings; Export documentation to support shipping. Essential Job Functions:
Niles, IL · On-site
S. FDA regulations, leadership skills, and experience bringing regulated consumer health care ... Labeling & Claims Review * Regulatory Documentation and Submissions * Quality & Risk Management
Niles, IL · On-site
S. FDA regulations, leadership skills, and experience bringing regulated consumer health care ... Labeling & Claims Review * Regulatory Documentation and Submissions * Quality & Risk Management
Chicago, IL · On-site
$80K - $112K/yr
FDA formulation and labeling requirements to navigate complexity, manage risk, and support cross-functional teams throughout the product lifecycle. The Senior Regulatory Specialist will also play an ...
Chicago, IL · On-site
$80K - $112K/yr
FDA formulation and labeling requirements to navigate complexity, manage risk, and support cross-functional teams throughout the product lifecycle. The Senior Regulatory Specialist will also play an ...
Chicago, IL · On-site
$80K - $112K/yr
FDA formulation and labeling requirements to navigate complexity, manage risk, and support cross-functional teams throughout the product lifecycle. The Senior Regulatory Specialist will also play an ...
Chicago, IL · On-site
$80K - $112K/yr
FDA formulation and labeling requirements to navigate complexity, manage risk, and support cross-functional teams throughout the product lifecycle. The Senior Regulatory Specialist will also play an ...
Deerfield, IL · On-site
Ensure that discussions regarding off-label use are handled transparently, following FDA guidelines for scientific exchange. Collaboration and Feedback: * Partner with internal teams (e.g., clinical ...
Deerfield, IL · On-site
Ensure that discussions regarding off-label use are handled transparently, following FDA guidelines for scientific exchange. Collaboration and Feedback: * Partner with internal teams (e.g., clinical ...
Ensure that discussions regarding off-label use are handled transparently, following FDA guidelines for scientific exchange. Collaboration and Feedback: * Partner with internal teams (e.g., clinical ...
Ensure that discussions regarding off-label use are handled transparently, following FDA guidelines for scientific exchange. Collaboration and Feedback: * Partner with internal teams (e.g., clinical ...
Lead and support FDA 510(k) submissions and other regulatory filings required to commercialize ... Evaluate product, software, manufacturing, labeling, supplier, and process changes to determine ...
Lead and support FDA 510(k) submissions and other regulatory filings required to commercialize ... Evaluate product, software, manufacturing, labeling, supplier, and process changes to determine ...
Lead and support FDA 510(k) submissions and other regulatory filings required to commercialize ... Evaluate product, software, manufacturing, labeling, supplier, and process changes to determine ...
Lead and support FDA 510(k) submissions and other regulatory filings required to commercialize ... Evaluate product, software, manufacturing, labeling, supplier, and process changes to determine ...
Joliet, IL · On-site
Forms include daily production report, FDA log sheet, Label Verification form, Calibration form and Bulk log sheet. Tests all gases and documents results on compression log report accurately and ...
Joliet, IL · On-site
Forms include daily production report, FDA log sheet, Label Verification form, Calibration form and Bulk log sheet. Tests all gases and documents results on compression log report accurately and ...
Joliet, IL · On-site
Forms include daily production report, FDA log sheet, Label Verification form, Calibration form and Bulk log sheet. Tests all gases and documents results on compression log report accurately and ...
Joliet, IL · On-site
Forms include daily production report, FDA log sheet, Label Verification form, Calibration form and Bulk log sheet. Tests all gases and documents results on compression log report accurately and ...
$10.65 - $11.28
3% of jobs
$11.28 - $11.91
3% of jobs
$11.91 - $12.54
11% of jobs
$12.78 is the 25th percentile. Wages below this are outliers.
$12.54 - $13.17
21% of jobs
The median wage is $13.75 / hr.
$13.17 - $13.80
13% of jobs
$13.80 - $14.43
11% of jobs
$14.43 - $15.06
4% of jobs
$15.51 is the 75th percentile. Wages above this are outliers.
$15.06 - $15.69
13% of jobs
$15.69 - $16.32
14% of jobs
$16.32 - $16.95
3% of jobs
$16.95 - $17.58
4% of jobs
$10
$14
$17
For Fda Labeling jobs in Chicago, IL, the most frequently searched job titles are:
The top searched job categories for Fda Labeling jobs in Chicago, IL are:
$62K - $93K/yr
Full-time
Medical, Life, Retirement, PTO
Posted 19 days ago
7.6
Based on 252 frontline employees who took The Breakroom Quiz
229th of 545 rated manufacturers
Job Summary
Medline Industries has an immediate opening for an Associate Regulatory Labeling Specialist. This role will be based out of our Northfield, IL corporate headquarters and will work a hybrid model.Job Description
JOB SUMMARY Under direct supervision, responsible for support of labeling projects through review and alignment of product artwork content with state and federal regulations. MAJOR RESPONSIBILITIES - Review, verify and complete packaging submission to graphic design team authorizing label related content based on product's regulatory structure and documented product claims support. Evaluate supporting documentation for relevance to desired product claims. - Review, approve and document product labeling, (packaging/collateral) for compliance to product's regulatory structure and QMS requirements. - Interpret and analyze state and federal regulations to ensure product labels are accurate and in compliance. - Periodic audit of historic files, processes, databases, etc. and maintenance of company/department databases, logs, and files. - Using a customer service approach, timely and effective communication and support of internal customers (product divisions). - Support trainingof divisional personnel on regulatory product structure, regulatory labeling requirements, and Medline's labeling procedure(s). MINIMUM JOB REQUIREMENTS Education - Bachelor's Degree or High School Diploma with at least 4 years relevant job experience. Work Experience - Experience providing customer service to internal and external customers, including meeting quality standards for services and evaluation of customer satisfaction. - Experience in processing all relevant details, evaluating and prioritizing their importance, and drawing clear and concise conclusions. Knowledge / Skills / Abilities - Experience using MS Office Suite products (Word, Excel, PowerPoint, Outlook). - Experience using time management skills to prioritize, organize, and track details in order to meet deadlines of multiple projects. PREFERRED JOB REQUIREMENTS Education - Bachelor's Degree in a science related field. Work Experience - 1 year of experience in a Quality or Regulatory role for a regulated industry. Knowledge / Skills / Abilities - Basic knowledge and understanding of FDA product codes and product class structure, Quality Management Systems and Good Manufacturing Practices, or willingness to learn through training and independent research. - Excellent communication and relationship building skills. Project management, critical thinking and problem solving abilities to deliver results and meet deadlines. - Work experience in evaluating information to determine compliance with standards, laws, and regulations.Medline Industries, LP, and its subsidiaries, offer a competitive total rewards package, continuing education & training, and tremendous potential with a growing worldwide organization.
The anticipated salary range for this position:
$62,000.00 - $93,000.00 AnnualThe actual salary will vary based on applicant's location, education, experience, skills, and abilities. This role is bonus and/or incentive eligible. Medline will not pay less than the applicable minimum wage or salary threshold.
Our benefit package includes health insurance, life and disability, 401(k) contributions, paid time off, etc., for employees working 30 or more hours per week on average. For roles where employees work less than 30 hours per week, benefits include 401(k) contributions, paid time off, as well as access to the Employee Assistance Program, Employee Resource Groups and the Employee Service Corp. For a more comprehensive list of our benefits please click here.
We're dedicated to creating a Medline where everyone feels they belong and can grow their career. We strive to do this by seeking diversity in all forms, acting inclusively, and ensuring that people have tools and resources to perform at their best. Explore our Belonging pagehere.
Medline Industries, LP is an equal opportunity employer. Medline evaluates qualified individuals without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, age, disability, neurodivergence, protected veteran status, marital or family status, caregiver responsibilities, genetic information, or any other characteristic protected by applicable federal, state, or local laws.
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Medline Industries, LP is the leading nationwide supplier of medical, surgical and pharmaceutical products to hospitals, nursing homes, HME providers, surgery centers, physician offices and home care/hospice settings.
Medical equipment and supplies manufacturing
10,000+ Employees
Winnetka, IL, US
1966
