Senior Associate/Strategist – Regulatory Affairs (APAC CMC)

Responsibilities

• Authoring regulatory submissions : Writing and reviewing the CMC sections for new e.g. New Drug Applications (NDAs), and Marketing Authorization Applications (MAAs) and lifecycle maintenance regulatory filings including responses to Health Authority’s questions.
• Ensuring regulatory compliance : Making sure that all documents align with the requirements of regulatory bodies as well as International Council for Harmonisation (ICH) guidelines.
• Collaborating with subject matter experts (SMEs) : Working closely with scientists, quality assurance (QA), manufacturing teams, and regulatory affairs colleagues to gather accurate and complete information about a drug's composition, manufacturing process, and quality control.
• Maintaining document quality : Ensuring completion of high-quality documents i.e. clear, concise, scientifically accurate, and consistent in style and format, complying with regulatory guidelines and internal processes within timelines.
• Managing timelines : Adhering to strict project schedules to ensure timely completion of submissions.
• Identify, Assess and Communicate potential CMC Regulatory issues and propose mitigation strategies .
• Understands, interprets and guides teams on regulations and policies related to manufacture and control of medicinal products to expedite the submission, review and obtain approvals.

Essential skills and qualifications

• Educational background : A bachelor's degree or higher in a scientific field, such as Chemistry, Pharmaceutical Sciences, or a related discipline.
• Experience : Minimum of 5 ~ 9 years of relevant work experience working within a Regulatory Affairs Department with direct accountability for deliverables.
• Pharmaceutical experience : Prior experience authoring CMC sections for regulatory submissions is a standard requirement.
• Technical writing expertise : Exceptional technical writing, editing, and communication skills are required to translate complex scientific data into clear regulatory documentation.
• Regulatory knowledge : A strong knowledge of CMC regulatory requirements for multiple global regions (e.g., APAC, U.S., EU) is essential. Experience with the electronic Common Technical Document (eCTD) format is also crucial.
• Industry familiarity : A background in pharmaceutical manufacturing or quality control is often beneficial.
• Collaboration and project management : The ability to work independently, manage projects, and communicate effectively with cross-functional teams is critical.
• Detail-oriented : Meticulous attention to detail is necessary to ensure the accuracy and completeness of submissions.