Welcome Back

Google icon Sign in with Google
OR
I agree to abide by Pharmadaily Terms of Service and its Privacy Policy

Create Account

Google icon Sign up with Google
OR
By signing up, you agree to our Terms of Service and Privacy Policy
Instagram
youtube
Facebook

Lead Executive - Labeling

Apotex
3+ years
Not Disclosed
Mumbai, India
1 June 3, 2026
Job Description
Job Type: Full Time Education: M.Pharm/B.Pharm or M.Sc. Skills: ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding

Lead Executive - Labeling

Company: Apotex
Location: Mumbai, Maharashtra, India
Job Type: Full-Time

About Apotex

Apotex is a Canadian-based global health company committed to improving access to affordable, innovative medicines and health products worldwide. With a diverse portfolio of generic, biosimilar, branded pharmaceuticals, and consumer health products, Apotex serves millions of patients across global markets.

Position: Lead Executive - Labeling

Job Summary

The Lead Executive - Labeling will be responsible for preparing and compiling regulatory labeling submissions for Health Canada, managing submission projects through DocuBridge, creating and maintaining BLUE projects, and ensuring accurate tracking of regulatory activities.

Key Responsibilities

Regulatory Submission Management

  • Prepare all required forms and documents for Health Canada submission projects.

  • Submit regulatory projects through DocuBridge within defined timelines.

  • Coordinate peer review activities and address reviewer comments promptly.

  • Create and maintain regulatory records in RIMS, CCR-QMS, LAMS, and BLUE systems.

  • Compile and upload submission packages for Health Canada.

Labeling and Artwork Review

  • Prepare text comparison reports for package insert verification.

  • Review and verify labels using proof comparison tools in BLUE.

  • Ensure accuracy, consistency, and compliance of packaging artwork and labeling documents.

  • Perform detailed proofreading of technical and regulatory documents.

Documentation and Compliance

  • Maintain regulatory trackers and project tasks.

  • Ensure all assigned training programs are completed on time.

  • Participate in webinars, meetings, and departmental training sessions.

  • Collaborate with Global Team Associates (GTA) and cross-functional teams on project activities.

  • Adhere to company quality standards, regulatory requirements, and compliance programs.

Team Collaboration

  • Communicate effectively with internal stakeholders and regulatory teams.

  • Support a collaborative work environment to achieve departmental goals.

  • Demonstrate Apotex core values: Collaboration, Courage, Perseverance, and Passion.

Qualifications

Education

  • M.Pharm, B.Pharm, or equivalent degree.

Experience

  • Prior labeling experience in any regulated market such as:

    • United States (USFDA)

    • Canada (Health Canada)

    • Europe

    • Rest of World (ROW)

Required Skills

  • Basic understanding of regulatory requirements for labeling submissions.

  • Strong document preparation and compilation skills.

  • Excellent proofreading and attention-to-detail abilities.

  • Good written and verbal communication skills.

  • Ability to review packaging artwork and technical specifications.

  • Self-motivated with strong ownership and initiative.

  • Effective team collaboration and interpersonal skills.

Preferred Competencies

  • Experience with regulatory submission systems and workflows.

  • Knowledge of Health Canada labeling requirements.

  • Familiarity with DocuBridge, RIMS, BLUE, and related regulatory systems.

  • Strong organizational and project management skills.

Location

Mumbai, Maharashtra, India