Executive Regulatory Labeling – Regulatory Affairs | Apotex | Mumbai, Maharashtra, India
Apotex is conducting a walk-in drive for the position of Executive Regulatory Labeling for its pharmaceutical regulatory affairs operations located in Mumbai, Maharashtra, India. This full-time opportunity is suitable for candidates with 3 to 6 years of experience in regulatory labeling, pharmaceutical documentation, labeling compliance, regulatory submissions, artwork coordination, quality review, and compliance management within regulated pharmaceutical environments. The selected candidate will support labeling operations, coordinate regulatory documentation activities, review product labeling content, maintain compliance records, coordinate with internal teams, and ensure adherence to global pharmaceutical regulatory standards. Candidates having expertise in pharmaceutical labeling systems, regulatory affairs operations, compliance documentation, and regulatory coordination activities will be preferred. This role provides valuable exposure to global pharmaceutical regulatory environments, labeling systems, compliance-driven workflows, and quality documentation operations focused on regulatory accuracy, product compliance, documentation management, and operational efficiency.
Location
Mumbai, Maharashtra, IndiaEmployment Type
Full-timeWalk-in Interview
YesWalk-in Date
2026-05-30Experience Required
3 to 6Compensation & Benefits
Competitive salary package with exposure to pharmaceutical regulatory systems, labeling operations, and long-term professional growth opportunities.About Apotex
Apotex operates in the pharmaceutical industry specializing in regulated manufacturing systems, healthcare products, and global regulatory operations.Position Overview
The Executive Regulatory Labeling will support pharmaceutical labeling systems, regulatory documentation, and compliance coordination activities.Key Responsibilities
- Review pharmaceutical product labeling and artwork documentation.
- Support regulatory labeling compliance activities.
- Coordinate regulatory submission and documentation processes.
- Maintain labeling records and compliance systems.
- Coordinate with quality assurance and regulatory teams.
- Ensure adherence to pharmaceutical regulatory standards.
- Participate in compliance reviews and documentation discussions.
- Monitor workflow and documentation accuracy.
- Support process improvement and operational efficiency initiatives.
- Maintain discipline within regulatory documentation systems.
Required Skills & Competencies
- Strong understanding of pharmaceutical regulatory labeling systems.
- Knowledge of regulatory documentation and compliance workflows.
- Communication and coordination capabilities.
- Problem-solving and analytical thinking abilities.
- Awareness of pharmaceutical GMP and regulatory standards.
- Attention to documentation accuracy and compliance quality.
- Time management and multitasking abilities.
- Technical reporting and regulatory coordination skills.
- Ability to work within compliance-driven environments.
- Adaptability to pharmaceutical regulatory operations.