CMC Writer Paramus, NJ

ESR Healthcare; Paramus (NJ); On-site; USD 101,920; Full time

Job summary

A leading company in pharmaceuticals is seeking a CMC Writer in Paramus, NJ. This role involves authoring regulatory documents such as NDA and MAA applications, ensuring compliance with FDA and EMA guidelines. The ideal candidate will have a background in chemistry or pharmaceutical sciences, along with experience in regulatory writing, demonstrating strong project management and collaboration skills.

Qualifications

• Experience in pharmaceutical or regulatory writing.
• Prior CMC Writer experience.

Responsibilities

• Author and review CMC sections of regulatory submissions, including IND, NDA, and MAA applications.
• Ensure documents align with FDA, EMA, and ICH requirements.
• Work with scientists and regulatory affairs teams to gather data.

Skills

Regulatory Documentation

Quality Assurance

Project Management

Collaboration

Process Improvement

Education

Bachelor's or advanced degree in chemistry, pharmaceutical sciences, or a related field

Job description

CMC Writer Paramus, NJ

CMC Writer, Chemistry, Manufacturing, and Controls, Regulatory, Drug Development, Manufacturing, and Quality Control, NDA/MAA CTD, EU (IMPD and MAA), US-FDA, FDA, IND, BLA, NDA, eCTD, Project Management, Pharmaceutical

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Experience level: Mid-senior Education level: Bachelor’s degree Job function: Health Care Provider Industry: Pharmaceuticals Pay rate : $49 per hour Total position: 1 Relocation assistance: No Visa sponsorship eligibility: No
SUMMARY:

A Pharmaceutical CMC (Chemistry, Manufacturing, and Controls) Writer plays a crucial role in regulatory submissions by preparing technical documents related to drug development, manufacturing, and quality control.
JOB DESCRIPTION:

Authors a range of clinical documents, including regulatory documents following defined templates, NDA/MAA CTD submission documents, investigator brochures, briefing documents, and responses to regulatory authority questions.
Support the coordination and preparation of timely CMC file for AR/DSUR/RTQ submissions
Authoring and review of CMC submission components and documentation in CTD to support regulatory submissions for mainly EU (IMPD and MAA) and US-FDA (IND, BLA or NDA) submissions
Ensure completion of high-quality submissions, following regulatory guidelines and internal processes within timelines.
Obtain information from other departments regarding regulatory submissions or documentation to support CMC submissions.
Assess and communicate potential regulatory risks and propose mitigation strategies
Understands, interprets and advises teams on regulations, guidelines, procedures and policies relating to manufacture and control of medicinal products, to expedite the submission, and review and approval of applications.
Identify, communicate and escalate potential CMC regulatory issues, as needed
Help establish regulatory CMC submission processes and procedures.
Familiar with eCTD format submission files
Project management skill is plus
KEY RESPONSIBILITIES:

Regulatory Documentation: Author and review CMC sections of regulatory submissions, including IND, NDA, and MAA applications.
Compliance & Guidelines: Ensure documents align with FDA, EMA, and ICH regulatory requirements.
Collaboration: Work closely with scientists, regulatory affairs teams, and manufacturing experts to gather accurate data.
Quality Assurance: Maintain consistency, clarity, and accuracy in technical writing.
Process Improvement: Help establish regulatory CMC submission processes and procedures.
QUALIFICATIONS:

Education: Bachelor's or advanced degree in chemistry, pharmaceutical sciences, or a related field.

Experience:

Prior experience in pharmaceutical or regulatory writing.
CMC (Chemistry, Manufacturing, and Controls) Writer experience.