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Open nowPosted 3490 days ago

Regulatory specialist

Integrated Resources INC2,463 open roles

Where
Parsippany-Troy Hills, NJ, United States
Work mode
On site
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Your applicationOpen nowRegulatory specialistIntegrated Resources INC · Parsippany-Troy Hills, NJ, United States

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  3. 25 readersRecruiter, hiring manager, skeptic. Round after round.

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The clock on this job

Early applications get read.

12.3% of postings close within 7 days. Measured by our own scanner across the market. Integrated Resources INC postings stay open a median of 15 days.

Share of postings closed within
  1. 2.1%1 day
  2. 4.5%3 days
  3. 12.3%7 days
  4. 19.3%14 days
  5. 35.6%30 days
  6. 58.1%60 days
This job: posted 3490 days ago

Integrated Resources INC median: 15 days open

The posting

Company Description

IRI believes in commitment, Integrity and strategic workforce solutions.

Integrated Resources, Inc., is led by a seasoned team with combined decades in the industry. We deliver strategic workforce solutions that help you manage your talent and business more efficiently and effectively. Since launching in 1996, IRI has attracted, assembled and retained key employees who are experts in their fields. This has helped us expand into new sectors and steadily grow.

We’ve stayed true to our focus of finding qualified and experienced professionals in our specialty areas. Our partner-employers know that they can rely on us to find the right match between their needs and the abilities of our top-tier candidates. By continually exceeding their expectations, we have built successful ongoing partnerships that help us stay true to our commitments of performance and integrity.

Our team works hard to deliver a tailored approach for each and every client, critical in matching the right employers with the right candidates. We forge partnerships that are meant for the long term and align skills and cultures. At IRI, we know that our success is directly tied to our clients’ success.

Job Description

  • The Regulatory Specialist will be responsible for activities to ensure product registration information is accurate and current.
  • The person will support the compilation, tracking, and processing of regulatory documentation (e.g., affiliate requests, technical documentation, regulatory submissions).
  • This individual will, also, be responsible to monitor and track the activities and expenses performed by vendors for Regulatory Operations ensuring a high-level of quality deliverables.
  • A minimum of 2 years of relevant professional experience in a business environment is required.
  • Experience in compiling regulatory documentation and/or obtaining CFG (Certificates to Foreign Governments) from FDA or CFS (Certificates of Free Sale) in Europe is preferred.
  • Must have ability to work both within a team and independently in a fast paced, changing environment.
  • Must possess clear verbal and written communication skills, attention to detail, strong organizational and project management skills and ability to problem solve, recognize and find solutions for gaps in processes.
  • Must be proficient with MS Office applications.

Additional Information

Regards,

Indu Dubey Clinical Recruiter 732-844-8725

indu @irionline.com

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