Job Details

ID #44726016
State New Jersey
City Summit
Job type Contract
Salary USD Depends on Experience Depends on Experience
Source Sunrise Systems, Inc.
Showed 2022-08-09
Date 2022-08-08
Deadline 2022-10-07
Category Et cetera
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Global Regulatory CMC Manager

New Jersey, Summit, 07901 Summit USA

Vacancy expired!

Sunrise System Inc. is currently looking for

Global Regulatory CMC Manager in

SUMMIT, NJ with one of our top clients.

Job Title: Global Regulatory CMC Manager

Job Id: 22-08884

Location: SUMMIT, NJ 07901

Duration: 6 months

Position Type: Hourly contract Position (W2 only)

NOTE: Company policy requires newly hired employees to be fully vaccinated for COVID-19 as of their start date. Company is an equal opportunity employer and will provide reasonable accommodation to the unvaccinated in accordance with federal, state, and local law.

Job Description:
  • PREREQUISITES BS/BA degree in Scientific Discipline (Masters or higher preferred) with
  • 5-7 years in the pharmaceutical industry, preferably with 1-3 years CMC regulatory experience

Responsibilities will include, but are not limited to, the following:
  • Participate in the development of the CMC regulatory strategy for small molecules, biologics and cell therapy submissions. These submissions include health authority briefing packages, IND/CTA, BLA/NDA and MAA regulatory filings.
  • Prepare and review CMC submission documents, registration dossiers, health authority briefing packages and responses to health authorities through collaborations with relevant line functions and with minimal supervision.
  • Responsible for the global regulatory evaluation of CMC change controls with supervision.
  • Responsible for the management of CMC activities related to developmental or commercial compounds, with supervision.
  • Represent Regulatory CMC on cross-functional development/commercial teams and Regulatory Affairs teams.
  • Participate in global regulatory interactions with health authorities, with supervision.
  • Facilitate document review meetings and discussions.
  • Develop and maintain knowledge of regulatory environment, regulations and procedures.

Skills/Knowledge Required:
  • Experience with CMC regulatory documents (IND/CTAs, BLA/NDAs, MAAs, responses, variations and briefing documents)
  • Knowledge of FDA, EMA and/or ICH guidelines and CMC regulations
  • Experience in drug development processes and post-approval requirements
  • Experience in developing CMC regulatory strategy
  • Experience in project management
  • Have a solution-oriented approach to problem solving
  • Ability to plan/prioritize work of group members and guide/develop others.
  • Ability to work on complex projects and within cross-functional teams with supervision
  • Excellent communication skills, both written and oral
  • -Change control (be able to work in CC systems i.e eQRMS, Infinity, Verity)

ContactManoj B| RecruiterDirect: 732 313 0283 | Email: Manoj.b@sunrisesys.comOrSatya | Delivery ManagerDirect: (732) 2720262 |Email: satya@sunrisesys.com

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