Regulatory Associate

Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 1996. Our mission centers on delivering only the best quality talent, the first time and every time. We provide quality resources in four specialty areas: Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing.

Title: Regulatory Associate

Duration: 6 Months (Possibility of Extension)

Location: Parsippany NJ

Job Responsibilities:

• Provide Regulatory Support for Current Products and Development Projects

• Execute strategy and provide regulatory support and input.

• Deliver projects and other initiatives to progress current product portfolio by providing regulatory direction and support to stakeholders:

• Collect and collate data required for registration submissions.

• Prepare submission packages for the appropriate Regulatory Agency.

• Correspond with the appropriate Federal or State Agency regarding registration submissions.

• Review product labeling and supporting materials.

• Implement New Regulations and Guidance’s

• Assess impact of new regulations and guidance’s.

• Work with stakeholders to implement requirements within specified timelines.

• Keep current with all relevant guidance’s and regulations while monitoring any changes that occur which may impact the current business.

• Assess and communicate all requirements to stakeholders in order to maintain compliance without delay to business due to regulatory issues.

• Adjust and monitor timelines to support the business.

• Support Infrastructure and Systems Integration

• Contribute to supporting a high quality and effective infrastructure to meet the regulatory requirements which support the launch of associated products within NA.

• Execute systems integration for optimal functionality and use.

• Contribution to infrastructure (processes, procedures, systems etc.) to be made within agreed upon timelines.

• Deliver project and brand specific activities assuring they are correct, complete and on-time including registrations, submissions, labeling/advertising initiation/reviews, etc.

• Gain Understanding of Legislative and Regulatory Climate

• Understand how the government operates and key touch points can access to influence policy development.

• Monitor trade associations and task forces that support .

• Monitor ongoing legislative and competitive developments.

• Monitor and gain an understanding of new policies and objectives involving federal and local government affairs.

• Review trade association materials (newsletters, meeting minutes, agenda items) to gain an understanding of where influencing opportunities exist.

• BA/BS degree required in the natural sciences.

• A minimum of 3 years of relevant work experience required.

• Experience with either EPA or FDA registered products is required.

• Experience in consumer products industry is highly preferred (a must if only experience is R&D).

• High attention to detail and strong organization skills

• Ability to establish close communications and working relationship with cross functional teams to meet business objectives

• Ability to work with uncertainties and effect innovative solutions to complex regulatory requirements

• Strong veal and written communication skills

• Strong negotiating, influencing and interpersonal skills

• Results oriented, entrepreneurial and self-motivated

• Excellent computer skills (Microsoft Office suite)

Feel free to forward my email to your friends/colleagues who might be available. We do offer referral bonus

Thank you for your time and consideration. I look forward to hearing from you!

Kind Regards

Ruchi Kumari

Clinical Recruiter

Integrated Resources, Inc.

IT Life Sciences Allied Healthcare CRO

Certified MBE |GSA - Schedule 66 I GSA - Schedule 621I

(DIRECT BOARD) # 732-844-8716 (F) 732-549-5549

LinkedIn: https://www.linkedin.com/in/ruchi-kumari

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