Job Description
Purpose
To manage and execute pharmaceutical manufacturing operations efficiently and compliantly, ensuring product quality,
productivity, and adherence to cGMP and regulatory requirements.
Position / Job Title
Sr. Executive Manufacturing
Department
Manufacturing
Reporting To
Asst. Manager/Manager/Sr. Manager
Location
Indore
Years Of Experience
48 years of experience in pharmaceutical manufacturing operations (formulation plant)
Dosage Form
Solid & Semi solid
Job Responsibilities / Deliverables
Manufacturing Operations
Execute and supervise manufacturing activities (dispensing, granulation, compression, coating, blending, filling as applicable).
Ensure manufacturing is carried out as per approved BMR,SOPs, and process parameters.
Achieve production targets with optimum utilization of manpower and equipment.
Monitor and control process parameters, yields, and material usage.
Documentation & Compliance
Review and ensure completion of Batch Manufacturing Records (BMR) and related GMP documents.
Ensure adherence to cGMP, GDP, data integrity, and safety guidelines.
Handle deviations, change controls, incidents, and CAPA related to manufacturing activities.
Support process validation, cleaning validation, and revalidation activities.
Quality & Regulatory Support
Coordinate with QA and QC for in-process checks and batch release activities.
Participate in internal audits, customer audits, and regulatory inspections (USFDA, WHO, EMA, etc.).
Ensure implementation of corrective and preventive actions.
Equipment & Manpower Management
Supervise and guide Executives, Operators, and Helpers.
Perform initial troubleshooting of equipment and coordinate with Engineering/Maintenance for breakdowns.
Ensure execution of preventive maintenance and calibration schedules.
Train team members on GMP, SOPs, and operational practices.
Safety & Continuous Improvement
Ensure compliance with EHS, 5S, and housekeeping standards.
Identify opportunities for process improvement, cost reduction, and efficiency enhancement.
Qualifications: B. Pharm / M. Pharm
Additional Notes Technical Skills & Knowledge
Strong hands-on experience in OSD / semi-solids manufacturing (as applicable).
Sound knowledge of GMP, validation, and regulatory requirements.
Experience Handling Regulated Market Batches Preferred.
Familiarity with QMS systems and documentation practices.
Behavioural & Leadership Skills
Team handling and decision-making skills
Strong communication and coordination abilities
Analytical and problem-solving mindset
Willingness to work in shifts
Preferred / Added Advantages
Exposure to new product introduction (NPI)
Experience in automation and modern manufacturing equipment
Knowledge of Lean manufacturing / Six Sigma
