Regulatory Affairs Specialist III
Position Overview
Job Description
JOB DESCRIPTION:
The Regulatory Affairs Specialist III works with a team of regulatory affairs professionals to ensure the establishment of best practices within the assigned area of responsibility.
Key responsibilities/essential functions:
- Support continuous improvement activities, including such areas as regulatory procedure development and documentation, standards compliance, and metrics development and implementation.
- Support regulatory compliance and optimization of quality system procedures relating to new product registration submissions and post market reporting through the development, maintenance and improvement of documented processes.
- Support regulatory inspections as required
- Work closely with regulatory, engineering, marketing, legal, and other professionals across the company to communicate company-wide programs and processes for regulatory compliance.
- Work with regulatory colleagues to ensure a consistent approach to regulations is adopted throughout the business within areas of responsibility.
- Collect & summarize performance metrics to identify program weaknesses & recommend improvements in procedures or oversight.
REQUIRED QUALIFICATIONS:
- Bachelor’s Degree (or international equivalent) in a related field such as: Regulatory Science, Biomedical Engineering, Biology, Chemistry, English (with a technical writing emphasis), Legal Studies, Law, Nursing, Physician Assistance, Pharmaceutical Science, Pharmacy OR minimum of 8 years progressive regulatory affairs experience in medical device or pharmaceutical industry or medical product regulation agencies, including knowledge and experience applying drug or device laws and regulations
- 5 years of relevant work experience
- Strong analytical skills
- Ability to work in a team environment with minimal supervision on projects and activities
- Ability to prioritize, plan & evaluate deliverables
- Knowledge & experience conducting scientific, regulatory, legal, or business research.
- Excellent verbal and written communication and presentation skills with the ability to communicate in English in an easy to understand manner
- Experience using spreadsheet and presentation software
Thanks
Warm regards
Avleen Kaur
732-318-6945
Perks & Benefits
About This Role
Integrated Resources Inc is seeking a Regulatory Affairs Specialist III to join their Regulatory Compliance team at the Mid level. This is a Contractor, Onsite position based in Phoenix, United States.
Interested candidates are encouraged to review the full job description above and apply through LegalAlphabet to be considered for this opportunity.
Practice Area
Regulatory Compliance
Position
Mid
Applicant Location Requirements
Applicants must be located in: US
Application Contact
Contact: Integrated Resources Inc Hiring Team
Application Deadline
June 26, 2026
Employment Type
Contractor
MEMBERS ONLY
$19/month = $228/year
$99/year
$0.27/day. Cancel anytime.
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