Full Description
Executive Manufacturing QMS jobs at chennai 2026
JD;
Key Responsibilities:
Responsible for preparation & review of the master documents of sterile manufacturing for parenteral facility.
Responsible for preparation and review of protocols and reports based on the requirements.
Responsible for document management and preparation like BMR s, BPR s, master SOP s etc.
Responsible for the handling of change
control, deviations, CAPA, investigation etc.
Responsible to give training to all the subordinates, technicians and operators of the department.
Responsible for Audit and compliance on manufacturing shopfloor.
Knowledge of kaizen and continuous improvements.
Qualification: BE / Btech
Experience: minimum 3 to 8 years experience in manufacturing QMS/Process review/Compliance.
Regards,
Nedhra -HR
89251 and 14937