Job Opening: Team Member – LCM at Cipla (Vikhroli)

Cipla, a global pharmaceutical company driven by the purpose of ‘Caring For Life,’ is inviting applications for the position of Team Member – LCM (Life Cycle Management) to join its Regulatory Affairs team.

Position and Requirements

Post: Team Member – LCM
Functional Area: Life Cycle Management (LCM)
Location: Vikhroli, Mumbai
End Date for Application: October 20, 2025

Requirement	Details
Qualification (Minimum)	Graduate in Pharmacy or Life Sciences.
Experience (Minimum)	2 years in the field of: Regulatory Affairs, Quality Assurance (QA), Quality Control (QC), Manufacturing, Analytical Development, or Research & Development (R&D).

Job Purpose and Key Accountabilities

The primary purpose of the role is to implement Life Cycle Management activities for Non-respiratory products across multiple global markets (including US, EU, South Africa, ANZ, WHO, PEPFAR & 150+ countries) to ensure business continuity and regulatory compliance.

Key responsibilities include:

Assessing Change Requests: Reviewing, evaluating, and categorizing change requests globally based on regulatory guidelines, and coordinating with various units (QA, R&D, manufacturing, regional teams) to get necessary documentation.
Preparing Variation Packages: Compiling variation packages (Modules 2 to 5) and deficiency responses for global submissions to support commercial launches and regulatory compliance.
Submitting Regulatory Reports: Preparing and compiling the Annual Report (US) and WHO Requalification Dossiers as per schedule to maintain product licenses.
Compiling Re-registration Dossiers: Assessing previous dossiers, coordinating document collection, and compiling re-registration dossiers to maintain product licenses in various countries.
Database Management: Maintaining and updating the product database for easy retrieval and tracking of change control closures, dossier submissions, and report statuses.