Technical competency in labeling Required: BS degree (or 3 years of equivalent experience in Regulatory Affairs) Additional Information Regards, _____ Pooja Mishra | Team Recruitment | Mindlance, Inc ...
Technical competency in labeling Required: BS degree (or 3 years of equivalent experience in Regulatory Affairs) Additional Information Regards, _____ Pooja Mishra | Team Recruitment | Mindlance, Inc ...
Summary/Objective The Senior Regulatory Affairs Associate is responsible for preparing submissions in eCTD format, actively participating in client meetings, interacting with the various governmental ...
Quick apply
Summary/Objective The Senior Regulatory Affairs Associate is responsible for preparing submissions in eCTD format, actively participating in client meetings, interacting with the various governmental ...
Summary/Objective The Senior Regulatory Affairs Associate is responsible for preparing submissions in eCTD format, actively participating in client meetings, interacting with the various governmental ...
Summary/Objective The Senior Regulatory Affairs Associate is responsible for preparing submissions in eCTD format, actively participating in client meetings, interacting with the various governmental ...
Summary/Objective The Senior Regulatory Affairs Associate is responsible for preparing submissions in eCTD format, actively participating in client meetings, interacting with the various governmental ...
Summary/Objective The Senior Regulatory Affairs Associate is responsible for preparing submissions in eCTD format, actively participating in client meetings, interacting with the various governmental ...
Regulatory Affairs Associate
Chandler, AZ · On-site
Cross-functional opportunities to multiple different areas in the company Support vendor qualification program and regulatory compliance projects to promote safe, quality products. • Follow all ...
Regulatory Affairs Associate
Chandler, AZ · On-site
Cross-functional opportunities to multiple different areas in the company Support vendor qualification program and regulatory compliance projects to promote safe, quality products. • Follow all ...
Regulatory Affairs Associate
Doral, FL · On-site
Health Care / Regulatory & Clinical Support Position Title: Junior or Assistant, Sales Support Division, Regulatory Team Summary Ability and knowledge to conduct the work listed in at least one of ...
Regulatory Affairs Associate
Doral, FL · On-site
Health Care / Regulatory & Clinical Support Position Title: Junior or Assistant, Sales Support Division, Regulatory Team Summary Ability and knowledge to conduct the work listed in at least one of ...
Regulatory Affairs Associate
Sylmar, CA · On-site
$40 - $45/hr
Bachelor's degree in a scientific or related discipline. * 1+ years of direct regulatory experience in the medical device field. * Recent experience with Class III implantable medical devices is ...
Quick apply
Regulatory Affairs Associate
Sylmar, CA · On-site
$40 - $45/hr
Bachelor's degree in a scientific or related discipline. * 1+ years of direct regulatory experience in the medical device field. * Recent experience with Class III implantable medical devices is ...
Regulatory Affairs Associate
Doral, FL · On-site
Health Care / Regulatory & Clinical Support Position Title: Junior or Assistant, Sales Support Division, Regulatory Team Summary Ability and knowledge to conduct the work listed in at least one of ...
Regulatory Affairs Associate
Doral, FL · On-site
Health Care / Regulatory & Clinical Support Position Title: Junior or Assistant, Sales Support Division, Regulatory Team Summary Ability and knowledge to conduct the work listed in at least one of ...
The Regulatory Affairs Generalist / Senior Associate provides comprehensive support across clinical, submission, and post approval regulatory activities for assigned pharmaceutical products and ...
The Regulatory Affairs Generalist / Senior Associate provides comprehensive support across clinical, submission, and post approval regulatory activities for assigned pharmaceutical products and ...
Regulatory Affairs Associate
Chandler, AZ · On-site
Cross-functional opportunities to multiple different areas in the company Support vendor qualification program and regulatory compliance projects to promote safe, quality products. Follow all company ...
Regulatory Affairs Associate
Chandler, AZ · On-site
Cross-functional opportunities to multiple different areas in the company Support vendor qualification program and regulatory compliance projects to promote safe, quality products. Follow all company ...
The Regulatory Affairs Generalist / Senior Associate provides comprehensive support across clinical, submission, and post approval regulatory activities for assigned pharmaceutical products and ...
The Regulatory Affairs Generalist / Senior Associate provides comprehensive support across clinical, submission, and post approval regulatory activities for assigned pharmaceutical products and ...
The Regulatory Affairs Associate Director, Globalization is responsible for alignment and execution of worldwide regulatory affairs strategies and practices related to their assigned area of focus ...
The Regulatory Affairs Associate Director, Globalization is responsible for alignment and execution of worldwide regulatory affairs strategies and practices related to their assigned area of focus ...
The Regulatory Affairs Associate Director, Globalization is responsible for alignment and execution of worldwide regulatory affairs strategies and practices related to their assigned area of focus ...
The Regulatory Affairs Associate Director, Globalization is responsible for alignment and execution of worldwide regulatory affairs strategies and practices related to their assigned area of focus ...
The Regulatory Affairs Associate Director, Globalization is responsible for alignment and execution of worldwide regulatory affairs strategies and practices related to their assigned area of focus ...
The Regulatory Affairs Associate Director, Globalization is responsible for alignment and execution of worldwide regulatory affairs strategies and practices related to their assigned area of focus ...
The Regulatory Affairs Associate Director, Globalization is responsible for alignment and execution of worldwide regulatory affairs strategies and practices related to their assigned area of focus ...
The Regulatory Affairs Associate Director, Globalization is responsible for alignment and execution of worldwide regulatory affairs strategies and practices related to their assigned area of focus ...
The Regulatory Affairs Associate Director, Globalization is responsible for alignment and execution of worldwide regulatory affairs strategies and practices related to their assigned area of focus ...
The Regulatory Affairs Associate Director, Globalization is responsible for alignment and execution of worldwide regulatory affairs strategies and practices related to their assigned area of focus ...
The Regulatory Affairs Associate Director, Globalization is responsible for alignment and execution of worldwide regulatory affairs strategies and practices related to their assigned area of focus ...
The Regulatory Affairs Associate Director, Globalization is responsible for alignment and execution of worldwide regulatory affairs strategies and practices related to their assigned area of focus ...
The Regulatory Affairs Associate Director, Globalization is responsible for alignment and execution of worldwide regulatory affairs strategies and practices related to their assigned area of focus ...
The Regulatory Affairs Associate Director, Globalization is responsible for alignment and execution of worldwide regulatory affairs strategies and practices related to their assigned area of focus ...
The Regulatory Affairs Associate Director, Globalization is responsible for alignment and execution of worldwide regulatory affairs strategies and practices related to their assigned area of focus ...
The Regulatory Affairs Associate Director, Globalization is responsible for alignment and execution of worldwide regulatory affairs strategies and practices related to their assigned area of focus ...
The Regulatory Affairs Associate Director, Globalization is responsible for alignment and execution of worldwide regulatory affairs strategies and practices related to their assigned area of focus ...
The Regulatory Affairs Associate Director, Globalization is responsible for alignment and execution of worldwide regulatory affairs strategies and practices related to their assigned area of focus ...
Regulatory Affairs Associate 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 associate jobs pay per hour?
As of Sep 14, 2026, the average hourly pay for regulatory affairs associate in the United States is $39.57, according to ZipRecruiter salary data. Most workers in this role earn between $31.73 and $46.88 per hour, depending on experience, location, and employer.
What is a regulatory affairs associate?
A regulatory affairs associate helps medical and pharmaceutical companies navigate regulatory approval processes so that products conform to all local, state, and federal regulations. As a regulatory affairs associate, you work with a team to obtain approval for products, maintain database systems for relevant information, and create reports required by federal or government agencies. You stay abreast of developments in legislation and regulation that may affect your company, and advise others on best practices for product development within a regulated framework.
What are the key skills and qualifications needed to thrive as a regulatory affairs associate, and why are they important?
To thrive as a Regulatory Affairs Associate, you need a solid background in life sciences or related fields, attention to detail, and knowledge of regulatory guidelines and standards. Familiarity with submission management systems, regulatory databases, and certifications such as RAC (Regulatory Affairs Certification) are highly valued. Strong organizational skills, effective communication, and the ability to work collaboratively are important soft skills in this role. These abilities ensure accurate documentation, timely regulatory submissions, and successful navigation of complex compliance requirements.
What are some common challenges regulatory affairs associates face when coordinating with cross-functional teams?
Regulatory Affairs Associates often collaborate closely with departments such as research and development, quality assurance, and marketing. A common challenge is ensuring all stakeholders understand and adhere to regulatory requirements, which may change frequently. Balancing project timelines with the need for accurate and compliant documentation can also be demanding, especially when teams have competing priorities. Effective communication and proactive planning are key to navigating these challenges successfully.
More about Regulatory Affairs Associate jobs
What cities are hiring for Regulatory Affairs Associate jobs?
Cities with the most Regulatory Affairs Associate job openings:
What are the most commonly searched types of Regulatory Affairs jobs?
The most popular types of Regulatory Affairs jobs are:
Who are the top companies hiring for Regulatory Affairs Associate jobs?
The top employers for Regulatory Affairs Associate jobs are:
What states have the most Regulatory Affairs Associate jobs?
States with the most job openings for Regulatory Affairs Associate jobs include:
What are popular job titles related to Regulatory Affairs Associate jobs?
For Regulatory Affairs Associate jobs, the most frequently searched job titles are:
Regulatory Affairs Associate
Huntsville, AL • On-site
Integrated Resources INC
• Recruiting and Staffing Services • 51 - 200 employees51 - 200 employees
Contractor
Re-posted 18 days ago
Job description
Company Description
At Mindlance, we strive to deliver value through the combination of right people, processes, technologies and program management solutions. Our methods include- applying domain expertise in specific industry segments, utilizing a highly-skilled workforce, leveraging a proven global delivery model, implementing structured and scalable quality processes and methodologies and yet, staying cost-effective
All in all, our expertise lies in providing trained and committed minds to help meet your business objectives, irrespective of the stage your business is in.
Job Description
Job Title: Labeling Assistant
Duration: 2 Months+
Location : Huntsville, AL
Summary:
Mark up the labeling (container and insert labels) and communicate the changes to the labeling vendor. Proof read the labeling for accuracy and formatting upon receipt from the vendor. Process the final labeling for approval and transmit the approved labeling to the vendor and internally to other groups like QA etc. File the approved labeling per Qualitest procedures and policies.
Job Description:
Performs routine cleaning and disinfection operations for the production support and process equipment according to Standard Operating Procedures (SOPs).
Prepare the draft labeling and coordinate with the labeling vendors to revise the labeling as directed by the supervisor
Proofs read the labeling upon receipt from the labeling vendor for accuracy, formatting and process the final labeling for review and approval internally within Qualitest and communicate the approvals to vendors.
Responsible to organize and file labeling files/folders (both electronic and paper based) as per Qualitest procedures and policies.
Maintain the log and status reports of labeling activities
Prepare side by side comparison of proposed labeling against current approved labeling for submission to the FDA
Qualifications
Qualifications
Good writing skills, strong organizational skills; detail oriented; proficient in MS Word, Adobe Acrobat and document scanning program, printing; strong interpersonal skills and excellent working relationship for interacting with internal/external customers; skilled at multi-tasking and prioritizing the workload; ability to work well independently or within a group with minimal supervision; ability to work effectively in a deadline-driven environment. Ability to utilize creative abilities and current practices to solve issues within the scope of the responsibilities. Knowledge of FDA requirements and understanding of pharmaceutical labeling
Preferred: Technical competency in labeling
Required: BS degree (or 3 years of equivalent experience in Regulatory Affairs)
Additional Information
Regards,
_________________________________________________________________________
Pooja Mishra | Team Recruitment | Mindlance, Inc. | Office: 732-243-0715
About Integrated Resources
Sourced by ZipRecruiter
Integrated Resources Inc (IRI), based in Edison, NJ, US, is an esteemed player in the staffing solutions industry with a credible presence on their official website irionline.com. Notably, IRI provides a range of professional staffing services including contract, contract-to-hire, and direct hire solutions to a wide spectrum of industries such as healthcare, life sciences, manufacturing, financial, insurance, and others. Since its inception, IRI has been committed to delivering top-talent and optimum solutions to meet its clients' diverse needs.
Industry
Recruiting and staffing services
Company size
51 - 200 Employees
Headquarters location
Edison, NJ, US
Year founded
1996