Regulatory Affairs Pharmacist

Job Purpose

Support the Regulatory Affairs function in its pre‑registration and/or post‑registration dossier submission activities by assisting in data gathering, screening, collating and compiling of the dossiers, post‑registration variations and any other documentation in order to submit the same to the Health Authorities for approval within the defined timelines as per overall objective of Cipla Medpro.

• eCDT/New dossier submissions and approvals – perform pre‑launch activities to ensure timely submission and registration of products within the defined timelines.
• Complete dossier audits/due diligences and Regulatory Affairs (RA) strategies as required.
• Complete specific pre‑registration activities including receipt, screening, compilation and timely submission of new dossiers, Quality, Inspectorate, Clinical and Naming & Scheduling responses to the Relevant Health Authority in line with the latest regulatory guidelines and in accordance with specific timelines committed to.
• Abide by the required standards, protocols and processes around obtaining dossiers and gathering supporting data from third party holders after signing of supply / purchase / financial agreements.
• Complete any required internal due diligences and risk reports to determine gaps ahead of time, and ensure that proper steps are taken, to proactively solve challenges in the registration process. This will ensure no delay at launch stage.
• Prepare new dossier submissions in e‑CTD systems, as required.
• Dossier Life Cycle Management – perform the dossier life cycle management activities by supporting the post‑registration variations and other activities to ensure support to the regulatory function and its objectives.
• Receive, prepare and submit all applicable updates, variations, resolutions and any other correspondence required by the SAHPRA or any other applicable regulatory authority to ensure timely delivery and as per the defined standards.
• Ensure compliance with the latest regulatory guidelines and prepares applications within specified timelines in order to support the business and strategic company objectives.
• Prepare variations in e‑CTD systems, as required.
• Conduct dossier due‑diligence in support of New Business Development projects.
• Support all new product launches/re‑launches, which includes (but not limited to): conducting dossier gap analysis to identify changes, artwork development, review and approval of artwork, variation preparations and submissions.
• Conduct any applicable engagement with SAHPRA or any other regulatory authority as part of follow‑up on a timely basis.
• Prepare post‑registration updates to professional information and patient information leaflets.
• Implement any changes in regulations and advise the applicable business units.
• Review and approval of all product artwork, in accordance with current Health Authority regulations and standards.
• Review and approval of change control documents, as and when required.
• Support the business with provision of dossier information, as required, e.g., documents required for tender applications.
• Support and assist the administrative team in the responsibility to effectively manage and maintain dossiers (electronically, ensuring smooth operations and maintaining quality standards).
• Ensure that the Document Database is kept up to date by completing the required administration activities for appropriate maintenance, coordination and accuracy of all dossiers and correspondence.
• Ensure quality check is time‑wise done before final submission to the applicable Health Authority.
• Complete any internal risk reports in line with the above submissions in order to avoid rejections / comebacks from any health authority.
• Develop and manage stakeholder relationships by communicating and interacting on a regular basis in order to achieve the functional objectives.
  • Build and proactively maintain critical relationships with the relevant Health authority to ensure streamlined pre‑registration and post‑registration submissions, evaluations and registrations.
  • Engagement to include; but not limited to face‑to‑face meetings, hard copy letters, telephone calls and emails.
  • Tracking of pre and post registration applications with the relevant Health authority for successful on time and in full approvals or registrations.
  • Align and collaborate with relevant Cipla India‑based stakeholders, local stakeholders and third‑party suppliers to ensure compliant, good quality dossiers are received to submit to the Health Authorities.
  • Build and maintain relationships with all external stakeholders, including 3rd party principals, industry bodies and consultants.
• Keeping abreast of developments and changes in the local regulatory and international environment which directly impacts Cipla products. Effectively communicating these changes to all relevant stakeholders to assess the impact on the business.