*Position:AGM/DGM - Production (Sterile Production – Cartridge)*
*Location: Vizag*
Key Responsibilities:
Manage endtoend sterile cartridge production operations.
Ensure adherence to cGMP regulatory and quality standards.
Plan schedule and monitor production activities to meet organizational targets.
Lead and mentor production teams fostering a culture of safety compliance and accountability.
Collaborate with QA QC Engineering and Supply Chain for seamless operations.
Drive process optimization cost efficiency and yield improvement initiatives.
Ensure proper documentation and batch records as per regulatory requirements.
Handle audits (regulatory customer internal) and implement corrective/preventive actions.
Monitor equipment performance and coordinate preventive maintenance.
Implement training programs for staff on sterile manufacturing practices.
*Requirements*
Education: / / . in relevant discipline.
Experience: 12–20 years in sterile manufacturing with significant exposure to cartridge production.
Strong knowledge of aseptic techniques regulatory guidelines (USFDA EU WHO) and validation practices.
Proven leadership and team management skills.
Excellent communication and problemsolving abilities.
*Position:AGM/DGM - Production (Sterile Production – Cartridge)**Location: Vizag*Key Responsibilities:Manage endtoend sterile cartridge production operations.Ensure adherence to cGMP regulatory and quality standards.Plan schedule and monitor production activities to meet organizational targets.Lead ...
*Position:AGM/DGM - Production (Sterile Production – Cartridge)*
*Location: Vizag*
Key Responsibilities:
Manage endtoend sterile cartridge production operations.
Ensure adherence to cGMP regulatory and quality standards.
Plan schedule and monitor production activities to meet organizational targets.
Lead and mentor production teams fostering a culture of safety compliance and accountability.
Collaborate with QA QC Engineering and Supply Chain for seamless operations.
Drive process optimization cost efficiency and yield improvement initiatives.
Ensure proper documentation and batch records as per regulatory requirements.
Handle audits (regulatory customer internal) and implement corrective/preventive actions.
Monitor equipment performance and coordinate preventive maintenance.
Implement training programs for staff on sterile manufacturing practices.
*Requirements*
Education: / / . in relevant discipline.
Experience: 12–20 years in sterile manufacturing with significant exposure to cartridge production.
Strong knowledge of aseptic techniques regulatory guidelines (USFDA EU WHO) and validation practices.
Proven leadership and team management skills.
Excellent communication and problemsolving abilities.
View more
View less