Production Head

4 - 5 years

0 Lacs

Posted:19 hours ago| Platform: Linkedin logo

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Work Mode

On-site

Job Type

Full Time

Job Description

Description:experience of 4-5 years in the same position preferred in Beta lactum Dry Powder Injectables and Dialysis fluids in Powder and Liquid forms.

Key Responsibilities

Production Operations

Plan, organize, and manage the overall production activities for the

Dry Powder Injectable section

.Ensure production targets are achieved as per monthly and annual schedules.Oversee

batch manufacturing

,

filling

,

lyophilization

, and

packaging

operations.Review and approve

BMRs (Batch Manufacturing Records)

,

SOPs

, and production documents.Coordinate with QA, QC, Engineering, and Stores for smooth plant operations.

Compliance & Quality

Ensure compliance with

cGMP, WHO, USFDA, and other international regulatory standards

.Prepare and face

regulatory audits

and client inspections.Ensure proper documentation, equipment qualification, and process validation.Monitor and maintain

cleanroom standards

and environmental controls.

People & Resource Management

Lead and mentor the

production team

, ensuring training, motivation, and performance management.Plan manpower requirements and ensure optimum utilization of workforce and resources.Promote a culture of

discipline, safety, and continuous improvement

.

Safety & Maintenance

Ensure strict adherence to

EHS (Environment, Health & Safety)

norms and aseptic practices.Coordinate preventive maintenance of machines and utilities with the Engineering department.Implement corrective and preventive actions for deviations and breakdowns.

Process Improvement & Cost Control

Drive

process optimization, yield improvement

, and

waste reduction

initiatives.Monitor production costs and ensure efficient utilization of materials and energy.Implement lean manufacturing and Kaizen practices.

Key Skills & Competencies

Strong technical expertise in

Dry Powder Injectable manufacturing and aseptic operations

.In-depth knowledge of

GMP documentation, validation, and regulatory compliance

.Excellent leadership, communication, and team management skills.Analytical and problem-solving mindset with attention to detail.Proficient in

MS Office, SAP/ERP systems

, and production data analysis.

Preferred Background

Experience in

parenteral formulations

, particularly

Dry Powder Injectables (Cephalosporin / Non-Cephalosporin)

.

Exposure To Regulatory Audits (WHO-GMP, USFDA, EU, MHRA, Etc.).

Hands-on experience with

lyophilization, filling line, and cleanroom management

.

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