What are the responsibilities and job description for the Sr. Manager-Director, Regulatory Affairs (Respiratory) position at Integrated Resources INC?
Company 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
REPORTING RELATIONSHIPS
Will report to President, R&D, USA. May be responsible for managing up to 2 RA staff including U.S. and India.
DUTIES & ESSENTIAL JOB FUNCTIONS
This position is responsible for all Regulatory Strategy and Filing aspects of MDI aerosols development, including CMC and possibly, Clinical strategy.
OTHER FUNCTIONS AND RESPONSIBILITIES
- Keep abreast of new Regulatory and Scientific developments in the Respiratory area.
- Additionally take on Derma & Transdermal RA responsibilities.
QUALIFICATIONS
- Regulatory experience supporting Generic Respiratory MDI aerosols development is a must!
- Good scientific/technical understanding of the MDI aerosols space
- Excellent written and spoken communication skills
- Excellent interpersonal skills
- Attention to details, quality and follow-through
- Project management and excellent time-management and organization skills
- Excellent analytical skills and problem solving ability
DUTIES & ESSENTIAL JOB FUNCTIONS
40% - Develop and provide Strategic Regulatory guidance/advice to Project Teams
30% - Manage all Regulatory aspects of Respiratory ANDA filings
20% - FDA interactions via e-mail, tel., mtgs, conferences
5% - Provide updates to senior & executive management
5% - Recruiting, training, team building
Qualifications
JOB DESCRIPTION
Education:
Master’s/PhD – in Chemistry/Pharm. Sciences
Experience:
- Must have MDI generics filing experience (not Nasal or other dosage forms); interacting with the FDA, developing Regulatory strategy
- 8 years total, and in MDI aerosol generics – 5 years
- Experience with regulatory agency interactions and preparation of documents for regulatory agency interactions
Additional Information
Thanks
Warm regards
Avleen Kaur
732-318-6945
