Job Description

Job Description

  • Compilation and/or initial review of labeling documents for OSD & Injectable for original ANDA and Additional strength submission.
  • Co-ordinate with CFT for involvement and understanding of priorities and filing timelines.
  • Follow-up with respective department to get documents in timely manner and to ensure that all labeling modules are available for submission on time.
  • To be updated with current labeling practices and regulatory guidelines.
  • Initial review of all deficiency & query responses related to US Labeling for both OSD and Injectable.
  • To ensure that all labeling modules are available for CR, IR and DRL submission on time. Co-ordination with cross-functional teams as needed to collect required documents for deficiency responses.
  • To compile deficiency responses.
  • Must Have knowledge for threshold analysis (labeling part only).
  • To achieve 100% launch readiness for all new products, with zero labeling issues. To ensure most recent and updated labeling has been issued Ok-To-Print. To ensure all printed labeling will be available for launch and on time. To ensure Drug listing of First Launch products after approval.
  • To ensure labeling docs are available on time for successful execution of Site Transfer projects.
  • To ensure labeling docs are available on time for successful execution of Additional Site Transfer activities.
  • Introduction of labeling for Third party.
  • Assist in review of all RLD updates of OSD & Injectable. To ensure that all labeling modules are available of RLD update for submission within time. To co-ordinate with supervisor for involvement and understanding of priorities.
  • Initiation/Facilitate Change Control and LRC for all labeling changes.
  • To approve Softcopy (vendor copy), transparency, shade card, First Print.
  • To create Barcode Grade report.
  • To address all annual reportable changes for labeling.
  • To compile labeling templates for Annual Report, PADER, and APQR.
  • Must have knowledge for Safety labeling change Notification.
  • Good hold on Patent and Exclusivity for labeling carve out.
  • Able to work on labeling SOPs.
  • Must have good English communication skill.

Qualifications

B. Pharm/M. Pharm


Job Details

Role Level: Not Applicable Work Type: Full-Time
Country: India City: Ahmedabad ,Gujarat
Company Website: http://www.amneal.com Job Function: Quality Assurance & Control
Company Industry/
Sector:
Pharmaceutical Manufacturing

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