RA RegCMC Manager

22時間前

Japan Sandoz Full time

Job Description Summary

-Responsible for regulatory activities specifically related to chemistry, manufacturing, and control (CMC). Activities such as the preparation & publication of REG CMC documentation for submissions to Health Authorities. In addition interact with HA's on REG CMC questions to support new product or post marketed launches.

Job Description

Major accountabilities: 

  • Lead CMC regulatory strategy with a focus on maximizing the business benefit balanced with regulatory compliance -Lead and implement all submission activities (planning, authoring, reviewing, coordination, submission) for assigned projects/products.

  • Identify the required documentation and any content, quality and/or timelines issues for submissions and complete submission and obtain approval in a timely manner in accordance with project timelines.

  • Author and/or review high-quality CMC documentation for HA submission, applying agreed CMC global regulatory strategies, current regulatory trends and guidelines.

  •  Ensure technical congruency and regulatory compliance, meeting agreed upon timelines and e-publishing requirements.

  • Prepare and communicate CMC Risk Management Assessments, contingency plans, and lessons learned on major submissions and escalate with management as appropriate.

  • Initiate and lead Health Authority interactions and negotiations as appropriate; setting objectives, preparing briefing books, coordinating and planning rehearsals and risk mitigation plans.

 Key performance indicators:

  • Produces high quality strategic project documentation and presentations; no late changes in strategy due to inadequate prior evaluation.

  • No delays in approvals of clinical studies, global registration dossiers or variations due to late or inadequate submission documentation on matters within RA CMC control.

  • Delivers reliable, timely and accurate information / communication about project specific issues within own department and to key stakeholders -RA CMC regulatory documentation follows Sandoz guidelines and meets regulatory guidelines.

  • Provides high quality regulatory evaluation and strategic advice on time (change control, etc.); regulatory compliance met in all compliance systems.

  • Maintains collaborative partnerships with stakeholders.

Minimum Requirements: 
 

  Work Experience:

  • Cross Cultural Experience.

  • Operations Management and Execution.

  • Collaborating across boundaries.

  • Project Management.

 Skills:

  • Change Control.

  • Cross-Functional Teams.

  • Documentation Management.

  • Negotiation Skills.

  • Project Management.

  • Regulatory Compliance.

  • Risk Assessment.

  • Risk Management.

 Languages :

  • English.

Skills Desired

Change Control, Cross-Functional Teams, Documentation Management, Negotiation Skills, Regulatory Compliance, Risk Assessment, Risk Management, Waterfall Project Management

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