Job Description: As a member of the team, you will be responsible for the following 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 BMRs, BPRs, master SOPs 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. Qualifications Required: - [Qualification 1] - [Qualification 2] - [Qualification 3] (Note: No additional details of the company were provided in the job description),

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Executive Manufacturing QMS and compliance Injectable