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Title : ALG- Global Regulatory Affairs - CMC -176
State : Texas   Date : Jan 4, 2021
Experience Level :  
Position Type : Global Regulatory Affairs - CMC      
Description
This position is for a leading pharmaceutical company. Below are the details of the engagement. If you are available and interested please send me your updated word resume & your expected hourly rate on W2 ASAP.
Looking forward to hearing from you soon.

Work Location: Fort Worth, TX

Job Title: Global Regulatory Affairs - CMC

Duration: 4+ months (extendable) contract on W2


Position Overview: 

This position will independently provide tactical and strategic leadership on complex CMC projects within the Global Regulatory Affairs organization by actively contributing to the development and implementation of global CMC regulatory strategies throughout the lifecycle of pharmaceuticals/devices. 

Main Areas Of Responsibilities: 

Independently lead global regulatory strategy development, planning, and implementation for multiple complex programs and platforms. Participate in identification of risk areas and develop alternative courses of action including anticipation of regulators responses through scenario planning and development of contingency plans. 
Guide and influence technical groups in areas of product lifecycle management and enhancement. 
Support the negotiating and decision making with regulators and stakeholders with complex and high-risk projects. 

Skills: 

Requirements: 
Experience in a pharmaceutical manufacturing facility/development laboratory preferred. 
Develop and implement regulatory strategy aligned with business strategy. 
Assess impact of new regulations and implement appropriate changes 
Support the Initiation and maintenance of appropriate communication within the RA function and stakeholders 
Participate in Due Diligence activities 
Interpret, apply and implement global regulations to CMC projects and prepare CMC regulatory submissions. 
Actively participate in project team meetings and provide leadership in meeting submission goals 
Identify and manage resolution to routine and complex issues including regulatory risk and provide risk/benefit strategies 

Preferred Skills/Qualification: 
Global responsibility for regulatory submissions 
Responsible for support of global registrations 
Sound basis of Scientific (Training/Communications) knowledge in multiple areas 
Expert knowledge of regulations, and experience with interpretation and application 
Excellent written and verbal communication, presentation, and facilitation skills 
Strong negotiation skills and significant experience in interacting with regulatory authorities 
Risk identification and problem solving skills.


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Many Thanks,   

Sree Kanth
Recruitment Manager
Sree@newageclinical.com

NewAgeSys, Inc.
Direct: 609-945-1736 Fax: 609-228-4079
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Princeton , NJ 08540 
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