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

4–8 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

Senior Executive