Pharmaceutical MES Program Leader

Drive MES excellence with Amaris Consulting as a Pharmaceutical MES Program Leader in Toronto.

This role offers a hybrid work mode and requires significant experience in program management.
The MES Program Manager will lead large-scale initiatives in a regulated pharmaceutical environment, leveraging 7-10 years of industry experience. Candidates should excel in managing complex stakeholder relationships, ensuring alignment of project objectives, and overseeing technical execution. A strong foundation in validation practices and regulatory compliance is essential.

Key Responsibilities:

• Lead MES projects through all development phases

• Coordinate across manufacturing, IT, and quality assurance teams

• Manage integrations with systems like PLCs and ERP platforms

• Ensure compliance in Computer System Validation processes

• Track program risks, budget, and resource allocations
Requirements:

• 7-10 years managing MES programs in pharma/biotech

• Proven experience in regulated manufacturing

• Strong knowledge of automation systems and GMP regulations

• Effective leadership in multidisciplinary settings

• Excellent communication and organizational skills
Position yourself as a vital part of a team that promotes quality and compliance in MES initiatives within the pharmaceutical domain.
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