Job Description

Overall Responsibilities

Production Planning

: Develop and implement production plans and schedules, ensuring timely delivery and cost-effective manufacturing.

Process Supervision

: Oversee batch manufacturing, monitor process validation, and maintain adherence to current Good Manufacturing Practices (cGMP), GDP, and regulatory norms.

Quality Assurance

: Perform quality checks, maintain product standards, investigate deviations, and manage audits, including those by agencies like US FDA, MHRA, and TGA.

Resource Coordination

: Ensure availability of raw materials, packaging materials, and machine readiness by liaising with procurement and other departments.

Documentation

: Prepare and maintain SOPs, batch records, and other production documentation in line with regulatory and company requirements.

Team Leadership

: Train, supervise, and motivate production staff; enforce company policies, safety procedures, and good manufacturing practices.

Continuous Improvement

: Analyze production data, recommend workflow optimizations, and lead efforts for process and quality improvement.
Educational Qualification

Minimum requirement

: Bachelor's degree in Pharmaceutical Sciences, Pharmacy, or related disciplines.

Preferred

: Master's degree and additional certifications in GMP, QA, or production management are advantageous. 4-10 years of relevant experience in OSD pharmaceutical manufacturing operations is typically expected.
Key Skills

Production planning and process validation Regulatory compliance and audit handling Documentation and reporting Leadership, teamwork, and training abilities Knowledge of equipment (granulation, compression, coating, etc.) and safety standards
Job Type: Full-time

Pay: ₹25,000.00 - ₹70,000.00 per month

Work Location: In person