Senior Regulatory Affairs Specialist

Integrated Resources Inc.; Cranbury Township (NJ); On-site; USD 60,000 - 80,000; Full time

Job summary

A leading staffing firm seeks a Regulatory Liaison to manage submissions and communicate with regulatory agencies. The candidate will prepare ANDAs and ensure compliance with FDA regulations. A BS or MS in a scientific discipline is required, along with 1-2 years in regulatory affairs.

Qualifications

• 1 - 2 years experience in pharmaceutical regulatory affairs mandatory.
• Experience with eCTD filings preferred.
• Regulatory Affairs Certification (RAC) is a plus.

Responsibilities

• Prepare ANDAs, supplements, and responses to FDA deficiency letters.
• Manage FDA review submissions (eCTD and SPL).
• Coordinate with functional groups for data submission.

Skills

Attention to detail

Excellent oral and written communication skills

Knowledge of US drug regulatory requirements

Education

BS or MS degree in a scientific discipline

Job description

A Few Words About Us
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.

Job Description

JOB SUMMARY

This will person will be a Regulatory liaison between product development and the regulatory agencies. This position will be responsible for regulatory submissions for new ANDAs and any changes being made to existing products. The position will also assist in labeling for new products, changes to labeling for existing prescription and OTC products. This position will also interact with other departments and cross functional teams both in US and India.

DUTIES & ESSENTIAL JOB FUNCTIONS

• Regulatory support of new and existing products including the preparation of ANDAs, supplements, Annual Reports, and responses to FDA deficiency letters/information requests.• Independently manage preparation (in paper or electronic formats (eCTD and SPL)), submission and monitoring progress of FDA review of ANDA's• Communication with functional groups for coordination and preparation of data for submission to FDA• Manage all Regulatory, Federal and State License requirements• Review change controls for regulatory requirements and according to appropriate regulations and guidance’s.• Familiar with Regulatory regulations (e.g. FDA guidance, ICH, 21 CFR etc)• Review labels as per FDA guidance• Regulatory support in drug listing.• Perform other duties as assigned

Qualifications

QUALIFICATIONS

• BS or MS degree in a scientific discipline, preferably Chemistry, Biology or Pharmacy• 1 - 2 years’ experience in pharmaceutical regulatory affairs (mandatory)• Attention to detail• Excellent oral and written communication skills• Knowledge of US drug regulatory requirements (mandatory)

REQUIREDBS or MS in Sciences or Pharmacy

PREFERREDExperience with eCTD filingsRegulatory Affairs Certification (RAC)

Additional Information

For more information contact me at 732-429-1858