Manufacturing QMS Head - Manager / Sr. Manager

Greetings from Zydus,

Production QMS Head

Key Responsibilities would be:

Responsible for monitoring of all manufacturing related activity performed in GEN & ONCO OSD facilities subjected to QMS .
To ensure effective implementation of organization vision, mission and goals at site to achieve the expectation. To provide leadership and direction to the QMS team. To participate in monthly Technical Review Meeting, ensure implementation of actions derived against this review and provide recommendations for continuous improvement. To support planning, scheduling and achieving production targets with optimum utilization of resources. Responsible for execution and closure of Quality Management system related activity. Responsible for monitoring and implementation of training programs in production area. Responsible for arranging and imparting technical training to personnel working in production area. Responsible for ensuring adequate training is imparted on a continuous basis and completion of training for all production personnel Responsible for compliance to Quality Management system and delivery schedules. Responsible for management of Internal and Regulatory Audit. Responsible for implementation of innovative ideas on the shop floor to improve productivity, system compliance and cost effectiveness. Responsible for allocation of Job to subordinates and follow-ups for completion of activity. Responsible for compliance with existing SOPs and procedures related to production area activity. Responsible to support for product failures investigations and other departmental deviations. Responsible for investigating and to evaluate quality issues during manufacturing along with quality team. To inform site head for any abnormalities i.e. deviations/events/safety events and other day-to-day activities and to participate in investigation activities. Support for QMS handling Initiation/Closure and closure related to Mfg./ Pkg./ Warehouse/ Engineering (CAPA, Track wise, Deviation, Process Validation, Batch records). Assessment of monitored CPPs and CQA of established products. To Support manufacturing team in course correction of events related to deviation, process challenges, OOS/OOT, Process improvements, etc. Responsible for coordination with Cross-functional team (GDSO /QA /QC /HR /WH /Engineering / EHS / PTC /IRA) for routine activity adherence. Responsible for review and approval of Quality Management system related documents of production area and other concern departments. Responsible for review and approval of various Documents related to GMP.

Interested candidates are requested to share their CVs on vaibhavi.harish2@zyduslife.com or Whatsapp on 6358958368.