This Global Regulatory Affairs (GRA) Labeling Associate position will ensure active adherence to the local and global labeling processes using the appropriate tools and systems to ensure ...
This Global Regulatory Affairs (GRA) Labeling Associate position will ensure active adherence to the local and global labeling processes using the appropriate tools and systems to ensure ...
Regulatory Affairs / Food Labeling
Hicksville, NY · On-site
$70K - $90K/yr
Regulatory Affairs Technician (Food Labeling) Who We Are: Nassau Candy is a leading manufacturer and distributor in the confectionery, gourmet food, and private-label industries. With decades of ...
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Regulatory Affairs / Food Labeling
Hicksville, NY · On-site
$70K - $90K/yr
Regulatory Affairs Technician (Food Labeling) Who We Are: Nassau Candy is a leading manufacturer and distributor in the confectionery, gourmet food, and private-label industries. With decades of ...
Associate Regulatory Affairs Labeling Associate
Lehi, UT · On-site +1
The Associate, Regulatory Affairs Labeling and Artwork (remote position): · Supports all aspects of product labeling and artwork development, review, approval, implementation and maintenance for ...
Associate Regulatory Affairs Labeling Associate
Lehi, UT · On-site +1
The Associate, Regulatory Affairs Labeling and Artwork (remote position): · Supports all aspects of product labeling and artwork development, review, approval, implementation and maintenance for ...
Associate Regulatory Affairs Labeling Associate
Lehi, UT · On-site +1
The Associate, Regulatory Affairs Labeling and Artwork (remote position): • Supports all aspects of product labeling and artwork development, review, approval, implementation and maintenance for ...
Associate Regulatory Affairs Labeling Associate
Lehi, UT · On-site +1
The Associate, Regulatory Affairs Labeling and Artwork (remote position): • Supports all aspects of product labeling and artwork development, review, approval, implementation and maintenance for ...
Director, Regulatory Affairs (Labeling)
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 ...
Director, Regulatory Affairs (Labeling)
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 ...
Director, Regulatory Affairs (Labeling)
$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
Director, Regulatory Affairs (Labeling)
$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 ...
Director, Regulatory Affairs (Labeling)
$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
Director, Regulatory Affairs (Labeling)
$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 ...
Position Description The Associate Labeling Specialist supports regulatory labeling strategy and quality system compliance within the Regulatory Affairs Labeling team at Applied Medical. This role ...
Position Description The Associate Labeling Specialist supports regulatory labeling strategy and quality system compliance within the Regulatory Affairs Labeling team at Applied Medical. This role ...
Position Description The Associate Labeling Specialist supports regulatory labeling strategy and quality system compliance within the Regulatory Affairs Labeling team at Applied Medical. This role ...
Position Description The Associate Labeling Specialist supports regulatory labeling strategy and quality system compliance within the Regulatory Affairs Labeling team at Applied Medical. This role ...
Labeling * Regulatory Authorities Qualifications Additional Information All your information will be kept confidential according to EEO guidelines.
Labeling * Regulatory Authorities Qualifications Additional Information All your information will be kept confidential according to EEO guidelines.
Position Description The Associate Labeling Specialist supports regulatory labeling strategy and quality system compliance within the Regulatory Affairs Labeling team at Applied Medical. This role ...
Position Description The Associate Labeling Specialist supports regulatory labeling strategy and quality system compliance within the Regulatory Affairs Labeling team at Applied Medical. This role ...
The Associate Director, Regulatory Affairs Labeling Product Leader will be responsible for the following: * Drive the global labeling strategy, including demonstrating an understanding of competitors ...
The Associate Director, Regulatory Affairs Labeling Product Leader will be responsible for the following: * Drive the global labeling strategy, including demonstrating an understanding of competitors ...
The Associate Director, Regulatory Affairs Labeling Product Leader will be responsible for the following: * Drive the global labeling strategy, including demonstrating an understanding of competitors ...
The Associate Director, Regulatory Affairs Labeling Product Leader will be responsible for the following: * Drive the global labeling strategy, including demonstrating an understanding of competitors ...
* Labeling * Regulatory Authorities Additional Information All your information will be kept confidential according to EEO guidelines.
* Labeling * Regulatory Authorities Additional Information All your information will be kept confidential according to EEO guidelines.
The Associate Director, Regulatory Affairs Labeling Product Leader will be responsible for the following: * Drive the global labeling strategy, including demonstrating an understanding of competitors ...
The Associate Director, Regulatory Affairs Labeling Product Leader will be responsible for the following: * Drive the global labeling strategy, including demonstrating an understanding of competitors ...
The Associate Director, Regulatory Affairs Labeling Product Leader will be responsible for the following: * Drive the global labeling strategy, including demonstrating an understanding of competitors ...
The Associate Director, Regulatory Affairs Labeling Product Leader will be responsible for the following: * Drive the global labeling strategy, including demonstrating an understanding of competitors ...
The Associate Director, Regulatory Affairs Labeling Product Leader will be responsible for the following: * Drive the global labeling strategy, including demonstrating an understanding of competitors ...
The Associate Director, Regulatory Affairs Labeling Product Leader will be responsible for the following: * Drive the global labeling strategy, including demonstrating an understanding of competitors ...
The Associate Director, Regulatory Affairs Labeling Product Leader will be responsible for the following: * Drive the global labeling strategy, including demonstrating an understanding of competitors ...
The Associate Director, Regulatory Affairs Labeling Product Leader will be responsible for the following: * Drive the global labeling strategy, including demonstrating an understanding of competitors ...
The Associate Director, Regulatory Affairs Labeling Product Leader will be responsible for the following: * Drive the global labeling strategy, including demonstrating an understanding of competitors ...
The Associate Director, Regulatory Affairs Labeling Product Leader will be responsible for the following: * Drive the global labeling strategy, including demonstrating an understanding of competitors ...
The Associate Director, Regulatory Affairs Labeling Product Leader will be responsible for the following: * Drive the global labeling strategy, including demonstrating an understanding of competitors ...
The Associate Director, Regulatory Affairs Labeling Product Leader will be responsible for the following: * Drive the global labeling strategy, including demonstrating an understanding of competitors ...
Regulatory Affairs Labeling information
See salary details
$18.99 - $22.95
3% of jobs
$22.95 - $26.90
6% of jobs
$26.90 - $30.86
13% of jobs
$31.38 is the 25th percentile. Wages below this are outliers.
$30.86 - $34.81
20% of jobs
The median wage is $36.35 / hr.
$34.81 - $38.77
19% of jobs
$38.77 - $42.72
9% of jobs
$44.70 is the 75th percentile. Wages above this are outliers.
$42.72 - $46.68
10% of jobs
$46.68 - $50.63
6% of jobs
$50.63 - $54.59
5% of jobs
$54.59 - $58.54
5% of jobs
$58.54 - $62.50
3% of jobs
$18
$39
$62
How much do regulatory affairs labeling jobs pay per hour?
What are some typical challenges faced in a Regulatory Affairs Labeling role?
Professionals in Regulatory Affairs Labeling often face the challenge of keeping up with frequently changing global regulations and ensuring all product labeling remains fully compliant. Managing tight deadlines while coordinating with cross-functional teams—such as clinical, legal, and marketing departments—can also be demanding. Additionally, interpreting complex regulatory language and translating it into clear, accurate, and user-friendly consumer information requires both technical acumen and attention to detail. Adaptability and proactive problem-solving help professionals excel in overcoming these challenges.
What are the key skills and qualifications needed to thrive in the Regulatory Affairs Labeling position, and why are they important?
To thrive as a Regulatory Affairs Labeling professional, you need thorough knowledge of regulatory guidelines, strong analytical skills, and experience in pharmaceutical or medical device labeling. Familiarity with document management systems, regulatory submission software, and certifications like RAC (Regulatory Affairs Certification) are often advantageous. Attention to detail, excellent communication, and strong organizational skills are key soft skills for success in this position. These abilities are essential to ensure labeling materials are accurate, compliant, and consistently meet evolving regulatory requirements.
What is a Regulatory Affairs Labeling job?
A Regulatory Affairs Labeling job involves ensuring that product labeling complies with regulatory requirements set by health authorities such as the FDA, EMA, or other global agencies. Professionals in this role develop, review, and manage labeling content, including packaging inserts, patient information, and safety warnings. They work closely with cross-functional teams, including regulatory, clinical, and marketing, to ensure accuracy and compliance. Their responsibilities also include tracking regulatory updates and implementing necessary label changes to meet evolving guidelines.
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Contractor
Posted 18 days ago
Job description
Artech Information Systems is the #12 Largest IT Staffing Company in the U.S. and an employer of choice for over 7,000 consultants. We recruit world-class talent for IT, engineering, and other professional jobs at 70+ Fortune and Global 500 companies coast-to-coast across the U.S., India, and China. We are one of the fastest-growing companies in the US and we welcome you to search the thousands of jobs in our cutting-edge GEM system for employment opportunities that fit your qualifications.
At the forefront of the staffing industry, Artech is a minority and women-owned business enterprise (MWBE) committed to maximizing global workforce solutions on behalf of its clients. Artech's deep heritage, proven expertise and insightful market intelligence has secured long-term partnerships with Fortune 500 and government clients seeking world-class professional resources.
This Global Regulatory Affairs (GRA) Labeling Associate position will ensure active adherence to the local and global labeling processes using the appropriate tools and systems to ensure harmonization and compliance with company and GMP standards and specifications. This Global Regulatory Affairs Labeling Associate role will have the specific duty to fully lead and write a United States Package Insert (USPI) for a particular assigned product in preparation for a US BLA submission.
This position will contribute to the Quality Enhancement Plan (QEP) through continuous and vigilant evaluation of labelling compliance via the Labelling Change Control process and the end to end labeling process flow. The position will do this by strictly following both local and global procedures. The Global Regulatory Affairs Labeling Associate will participate in scientific, technical and operational exchanges with Clinical Development, Pharmacovigilance, Medical Affairs, Marketing, Industrial Operations, Legal, Regulatory Affairs Franchise and Global Labeling as necessary to ensure labeling documents and associated change requests are medically and scientifically accurate and that they comply with company standards, and meet company needs.
Key Accountability:
Enhance the scientific contribution of the GRA Labeling group and work in concentration with Clinical Development, Pharmacovigilance and Medical Affairs on-site and/or globally.
Represent GRA Labeling department on product and project teams by interfacing with other functions and leading particular projects and products through completion and/or licensure where appropriate.
Achieve consistency in labeling and Regulatory labeling process through regulatory standards, cross functional collaboration and interactions with health authorities where appropriate.
Contribute to the label control, format and design of packaging for leaflets, cartons and labels of specific products and coordinate implementation of labeling components in collaboration with Industrial Operations where appropriate.
Actively participate in regulatory aspects of internal project plans and ensure timelines are met and milestones are achieved.
Focus will be on the details of the scientific/medical documentation required to ensure accurate and complete label development, evaluations, reviews, and approvals. Need to contribute to productive yet challenging relationships with cross-functional areas to ensure integrity and quality of Regulatory output.
Skills:
4-8 years prior Regulatory Affairs or relevant industry experience.
Demonstrated experience with biopharmaceuticals and management capability
Business Certification and/or experience preferred.
Bachelor's degree in scientific field preferred.
Advanced degree preferred.
For more information, Please contact
Best Regards,
Akriti Gupta
(973) 967-3409
Morristown, NJ 07960
About Artech
Sourced by ZipRecruiter
Artech is a leading IT staffing and consulting company based in Morristown, NJ, US. Since its foundation in 1992, Artech has mastered in complementing human expertise with technology and business acumen to produce world-class staffing solutions. The company caters to diverse industry sectors, including financial services, healthcare, telecommunication, energy and utilities, supply chain, and retail. It provides IT consulting, project management, professional and staff augmentation, and managed staffing services. Artech's mission is to provide exceptional IT staffing services to its clients by comprehending their business needs and then crafting a customized staffing strategy. Its notable achievement includes being recognized as one of the largest IT staffing companies in the U.S, according to Staffing Industry Analysts (SIA).
Industry
Recruiting and staffing services
Company size
10,000+ Employees
Headquarters location
Morristown, NJ, US
Year founded
1992