[Innovative Medicine] R&D, Scientist, CMC Group, CMC Sciences, Regulatory Affairs

<p style="text-align:left"><span>At Johnson &amp; Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com</span></p><p></p><p></p><p style="text-align:left"><b><span><span>Job Function: </span></span></b></p>Discovery &amp; Pre-Clinical/Clinical Development<p style="text-align:inherit"></p><p style="text-align:inherit"></p><p style="text-align:left"><b><span><span>Job Sub </span></span><span><span>Function: </span></span></b></p>Regulatory Science<p style="text-align:inherit"></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Job Category:</b></p>Scientific/Technology<p style="text-align:inherit"></p><p style="text-align:inherit"></p><p style="text-align:left"><b>All Job Posting Locations:</b></p>Chiyoda, Tokyo, Japan<p style="text-align:inherit"></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Job Description:</b></p><p><span style="color:#000000"><b>JOB SUMMARY:</b></span></p><ul><li style="text-align:left"><p><span style="color:#000000">To conduct change control of approved products appropriately as CMC-regulatory affairs (CMC-RA).</span></p></li><li style="text-align:left"><p><span style="color:#000000">To prepare application dossiers for CMC part and to communicate with HA appropriately to contribute in obtaining regulatory approval.</span></p></li></ul><p><span style="color:#000000"> </span></p><p><span style="color:#000000"><b>KEY RESPONSIBILITIES:</b></span></p><ul><li style="text-align:left"><p><span style="color:#000000">Change control activities for approved drug products as CMC-RA Regulatory Affairs (chemical and biological products)</span></p></li><li><ul><li style="text-align:left"><p><span style="color:#000000">Conduct regulatory assessment and develop regulatory strategy</span></p></li><li style="text-align:left"><p><span style="color:#000000">Collaborate with global and local stakeholders related to CMC-RA activity in Japan</span></p></li><li style="text-align:left"><p><span style="color:#000000">Prepare, review and conduct QC of the CMC part of the dossier (e.g. manufacturing process, specifications and test methods, and stability) with logical and scientific quality</span></p></li><li style="text-align:left"><p><span style="color:#000000">Prepare and reply to CMC questions from PMDA, and communicate directly with PMDA officials</span></p></li><li style="text-align:left"><p><span style="color:#000000">Conduct GMP inspection related activities</span></p></li><li style="text-align:left"><p><span style="color:#000000">Conduct regulatory consultations</span></p></li><li style="text-align:left"><p><span style="color:#000000">Conduct CRO management if the above activities are outsourced</span></p></li></ul></li></ul><p><span style="color:#000000">*</span> <span style="color:#000000">May be in charge of new drug application</span></p><p><span style="color:#000000"> </span></p><p><span style="color:#000000"><b>REQUIREMENTS:</b></span></p><p><span style="color:#000000">Experience/Knowledge</span></p><ul><li style="text-align:left"><p><span style="color:#000000">At least 3 – 5 years’ experience in CMC related arena in pharmaceutical industry</span></p></li><li style="text-align:left"><p><span style="color:#000000">Experience in change control operations (partial change applications) for post approved products several times</span></p></li><li style="text-align:left"><p><span style="color:#000000">Experience in preparation of CTD and application form several times</span></p></li><li style="text-align:left"><p><span style="color:#000000">Experience in CMC operations for multiple products including chemical products and biological products is desirable (including continuous manufacturing, antibodies, and cell &amp; gene therapy products)</span></p></li><li style="text-align:left"><p><span style="color:#000000">Experience in new drug application is also desirable</span></p></li></ul><p><span style="color:#000000">Qualification/Certificate</span></p><ul><li style="text-align:left"><p><span style="color:#000000">Practical level English skill (TOEIC ≥ 700)</span></p></li><li style="text-align:left"><p><span style="color:#000000">Bachelor, Master, Doctor</span></p></li></ul><p><span style="color:#000000"> </span></p><p><span style="color:#000000"><b>&#xff1c; For Internal Applicants&#xff1e;</b></span></p><ul><li style="text-align:left"><p><span style="color:#000000">If you are Japan employee, please read “Internal Application Guideline” in Ask GS. Especially if you are less than 18 months in your current role, you are required to obtain application approval from your current manager as well as your respective BUHR. If you are Japan’s employee, you are not able to apply for multiple positions at once.</span></p></li><li style="text-align:left"><p><span style="color:#000000">For Employee Referral Program (ERP), please read and understand the details of the “Employee Referral Program (ERP)” on the AskGS and you have made a compliant referral.</span></p></li></ul><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p> </p><p> </p><p><b>Required Skills: </b></p><p> </p><p> </p><p><b>Preferred Skills:</b></p>Analytical Reasoning, Coaching, Communication, Data Reporting, Drug Discovery Development, Execution Focus, Healthcare Trends, Process Oriented, Public Policies, Regulatory Compliance, Regulatory Development, Regulatory Reporting, Relationship Building, Risk Compliance, Scientific Research, Technical Writing, Technologically Savvy