Pfizer Senior Executive in Chennai, India

  • The MQA team associate will be responsible for supervising a specific shift to ensure that all manufacturing and packaging operations are operating within a state of cGMP compliance. This individual will supervise and coordinate the quality functions with guided oversight and will be responsible for communicating effectively and for providing direction to employees on such shifts. The MQA team member will be accountable for ensuring that all products manufactured meet the cGMP requirements based upon all regulatory requirements, and for also ensuring that an assigned shift is working within the parameters of quality systems. The MQA team member has the ability to shut down a production line if product is not meeting quality standards. The individual will ensure that when quality-related issues arise, these issues are quickly elevated, so that sufficient resources are applied to correctly investigate, document, and lead corrective actions.

  • Provide line clearance prior to commencement of manufacturing and during changeover.

  • Conduct in-process inspection during various manufacturing and packaging activities.

  • Monitoring of dispatch related activities like placement of data loggers, loading, downloading the data logger details etc...

  • Observe and report non-conformance to group lead-manufacturing quality assurance.

  • Review of master documents related to production.

  • Review of artworks related to printed packing materials.

  • Work in conjunction with management to ensure that all aspects related to site cGMP compliance are followed by employees.

  • Work with the MQ group lead to ensure that all manufacturing and control procedures and specifications are followed as they relate to production, processes and equipment.

  • Assure that the appropriate resources are utilized on a specific shift as they relate to CAPAs, root cause analysis, preventive actions, trending results and corrective actions, in accordance with facility standards and cGMP compliance.

  • Direct manufacturing staff to uphold quality and determine when manufacturing lines need to be shut down to investigate production issues.

Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.