Pharmaceutical CMC Writer (04+Months Contract)
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.
Apply Now
Apply Now
• 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.
Apply Now
Apply Now