Cmc Regulatory Documentation Analyst Remote New

apartmentStage Solutions Inc placeNew Brunswick calendar_month 

CMC Regulatory Documentation Analyst (Remote- New Brunswick, NJ)

We are seeking a CMC Regulatory Documentation Analyst for a global pharmaceutical client. You will be managing the documentation activities for marketing applications and/or post-approval regulatory submissions for cell therapy brands. This role may also require the preparation of some CMC dossier elements of regulatory filings for marketing applications and/or post-approval regulatory submissions for cell therapy brands.

This position regularly interfaces with experts in Manufacturing Sciences & Technology, Analytical Sciences, Quality and Regulatory departments.

This is a 40-hour per-week, 6-month contract (extensions possible), 100% remote role in New Brunswick, NJ.

This is a W2 role as a Stage 4 Solutions employee. Health benefits and 401K are offered.

Responsibilities:

  • Manage document preparation of CMC regulatory submission documents to BMS standards and ensure final document compliance to ensure submission content meets formatting requirements.
  • Manage the logistical process in the authoring system for CMC regulatory submissions.
This process includes coordinating reviews in the review and authoring system, assisting in the triage of comments, scheduling/facilitating consensus meetings, distributing review comments to the matrix teams.
  • Facilitate data verification to ensure the accuracy of submission data following the internal standard operating procedure. Author CMC elements of regulatory filings with supervision.
  • Participate on various cross-functional project teams, interact with technical subject matter experts, regulatory and other key partners both internal and external to the company as necessary.

Requirements:

  • 4 + years of experience in pharmaceutical or biotechnology industry.
  • Must possess working knowledge of regulatory CMC submissions, experience in Cell Therapy and CMC are a plus.
  • Must have a clear understanding of CMC submission structure with respect to the different Modules (1,2,3) and respective section numbering within those modules.
  • Experienced in Word is required. Ability to navigate in electronic systems.
  • Bachelor's degree

Please submit your resume to our network at (please apply to the CMC Regulatory Documentation Analyst (Remote- New Brunswick, NJ) role).

Please feel free to forward this project opening to others who may be interested.

Stage 4 Solutions is an equal-opportunity employer. We celebrate diversity and are committed to providing employees with an inclusive environment that is free of discrimination and harassment. All employment decisions are based on the job requirements and candidates' qualifications, without regard to race, color, religion/belief, national origin, gender identity, age, disability, marital status, genetic information, or other applicable legally protected characteristics.

Compensation: $35/hr. - $39.47hr.

#LI-SW1

placeLakewood (NJ), 30 mi from New Brunswick
Overview: YOUR PASSION, ACTIONS & FOCUS is our Strength Become one of our Contributors Join the KnipperHEALTH Team! The Document Control Specialist will be responsible for ensuring the efficient management and compliance of documentation...
apartmentEnglewood Lab, IncplaceTotowa, 33 mi from New Brunswick
Title: Quality Assurance (QA) Lead- Documentation and Product Release Reports to: Quality Assurance Supervisor or Manager Department: Quality Assurance Responsibilities:  •  Support Annual Drug and Device History Reviews.  •  Oversee and maintain...
apartmentNavitsPartnersplaceNew Brunswick
on clinical trial procedures, risks, and benefits.  •  Monitor patient responses to experimental treatments.  •  Maintain accurate clinical research documentation.  •  Collaborate with oncologists and pharmaceutical sponsors....