Executive - Strategic Manufacturing Projects

Job Description:

Responsibilities

• Drive execution of Quality & Regulatory Compliance (QRC) initiatives, ensuring alignment with global regulatory requirements and audit readiness.
• Support facility uplift initiatives, including equipment upgrades, system improvements, and compliance enhancement programs across sites.
• Facilitate Gemba Walkthroughs to identify gaps between SOPs and actual practices and drive timely closure of observations.
• Implement Mission-Based Training (MBT) and capability-building initiatives to enhance on-ground execution and sustain compliance behavior.
• Contribute to product robustness and process reliability programs to strengthen quality performance and inspection readiness.
• Collaborate with cross-functional teams and vendors to improve vendor efficiency, supply reliability, and compliance standards.
• Drive cultural and behavioral transformation, promoting a “Quality First” mindset through awareness programs, storytelling, and engagement initiatives.
• Ensure strong understanding and application of SOPs, regulatory guidelines, and process–practice alignment across operations.

Qualification & Experience

• Graduation in Pharmacy or Analytical Chemistry
• Post Graduation in Pharmaceutical Technology or Business Administration
• 2–3 years of experience in quality, regulatory compliance, or audit readiness functions
• Demonstrated exposure to regulatory audits and compliance programs
• Experience working in cross-functional teams and project-based environments