Valeant Pharmaceuticals

Manufacturing Control Specialist

Job ID
Pos. Type
Full Time


The purpose of this position is to perform nonconformance investigations, issue deviations, and complete corrective/preventive actions for the Manufacturing Depts.


Issue, investigate and write nonconformance investigations for the four manufacturing departments.  Recommend, implement and coordinate corrective actions including process changes and training with Quality Assurance.  Analyze material variance.  Support the training program for manufacturing personnel related to nonconformance events.  Provide trending of nonconformance events related to personnel and processes.  Provide feedback to management regarding the activities of the team, the plan for future improvements and identification of obstacles that could prevent or slow down the correction/improvement process.  Effectively work with support functions to assure prompt response is received.


Evaluation of quality issues with the MQA Manager and write investigation reports.  Assumes responsibility for the GMP, ISO, environmental health and safety procedure awareness and compliance within the respective area. Tracks and improves material variance and quality indicators.  Work closely with the area managers for training of operators to understand all aspects of the nonconforming event and serve as a facilitator to create a culture of continuous improvement. Writing and executing protocols as needed to improve process.


BS in related sciences


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