CMC Regulatory Scientist III
Company Name:
NewAgeSys, Inc
job
Title : CMC Regulatory Scientist III
Location : Rahway,NJ
Duration :6 Months with extension possibility
Job Details:
Qualifications:
B.S. degree in Chemistry, Pharmacy or Engineering related field. Minimum 3- 5 years Pharmaceutical regulatory experience with post- approval emphasis. Global experience preferred. Applicant should have experience conducting regulatory assessments, submission authoring and assembly using CTD structure, and eCTD lifecycle management. Proven organizational skills and excellent written/verbal communication are required. Applicant should have demonstrated writing skills, attention to detail and problem solving skills. Proficiency needed in MS Office programs (Word, Excel, Outlook).
Responsibilities:
The major responsibilities include: preparing and updating CMC sections of global Marketing Authorizations; executing regulatory post-approval filing strategies and variations for global products while ensuring that all regulatory documents are prepared accurately, completely and on-time; tracking project status and effectively communicating progress. Applicant will be responsible for multiple project assignments with critical timelines.
Kindly send your updated word format resume along with the following details
Work Authorization Status:
Compensation you expect :
Availability to start new
position
:
Date of birth and month :
End date of your (present or previous) Job :
Reason you to leave (present or previous) Job :
Best time and phone number to be reached
--
Also, please note we pay a referral bonus if we place any candidate you may refer. The referral bonus ranges from $1000 to $2000, depending on the positions.
Many Thanks,
Sujai Gopal
Clinical Resource Specialist
NewAge Clinical, A Division of NewAgeSys, Inc.
231 Clarksville Road, Suite 200, Princeton Junction, NJ 08550
Direct Tel # - 609-945-1722
Email :Estimated Salary: $20 to $28 per hour based on qualifications.
NewAgeSys, Inc
job
Title : CMC Regulatory Scientist III
Location : Rahway,NJ
Duration :6 Months with extension possibility
Job Details:
Qualifications:
B.S. degree in Chemistry, Pharmacy or Engineering related field. Minimum 3- 5 years Pharmaceutical regulatory experience with post- approval emphasis. Global experience preferred. Applicant should have experience conducting regulatory assessments, submission authoring and assembly using CTD structure, and eCTD lifecycle management. Proven organizational skills and excellent written/verbal communication are required. Applicant should have demonstrated writing skills, attention to detail and problem solving skills. Proficiency needed in MS Office programs (Word, Excel, Outlook).
Responsibilities:
The major responsibilities include: preparing and updating CMC sections of global Marketing Authorizations; executing regulatory post-approval filing strategies and variations for global products while ensuring that all regulatory documents are prepared accurately, completely and on-time; tracking project status and effectively communicating progress. Applicant will be responsible for multiple project assignments with critical timelines.
Kindly send your updated word format resume along with the following details
Work Authorization Status:
Compensation you expect :
Availability to start new
position
:
Date of birth and month :
End date of your (present or previous) Job :
Reason you to leave (present or previous) Job :
Best time and phone number to be reached
--
Also, please note we pay a referral bonus if we place any candidate you may refer. The referral bonus ranges from $1000 to $2000, depending on the positions.
Many Thanks,
Sujai Gopal
Clinical Resource Specialist
NewAge Clinical, A Division of NewAgeSys, Inc.
231 Clarksville Road, Suite 200, Princeton Junction, NJ 08550
Direct Tel # - 609-945-1722
Email :Estimated Salary: $20 to $28 per hour based on qualifications.
|
|
 | |
