CMC Writer

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.

Job Type: Full-time

Pay: $30.00 - $45.00 per hour

Application Question(s):

• Prior experience authoring CMC sections for regulatory submissions (IND, NDA, BLA, or MAA)?
• Ability to write and review documents in eCTD format?
• ) Do you have prior experience authoring CMC sections for regulatory submissions (e.g., IND, NDA, BLA, or MAA)? If yes, please specify which submissions you've worked on.
• How many years of experience do you have in pharmaceutical or regulatory writing?

Education:

• Bachelor's (Required)

Work Location: In person