Senior Validation Engineer in Pharmaceutical Manufacturing

Elevate your career with Amaris Consulting as a Senior Validation Engineer focused on pharmaceutical manufacturing in Toronto, ON. This hybrid role involves key responsibilities in quality validation and environmental monitoring.

Amaris Consulting seeks a Senior Validation Engineer to support its expansion project in sterile manufacturing. You’ll manage validation processes, ensuring compliance with GMP regulations, while leading strategies for isolator qualifications and aseptic processes. Your technical expertise will aid in maintaining high standards of quality assurance.

Key Responsibilities:

• Develop comprehensive EM validation programs

• Lead isolator and cleanroom qualification activities

• Design and execute aseptic process simulation campaigns

• Monitor validation study outcomes and analyze data

• Collaborate with multidisciplinary teams for project success

Requirements:

• Bachelor’s degree in Science or Engineering

• 7–10 years within GMP-regulated pharmaceutical settings

• Expertise in environmental monitoring and validations

• Knowledge of FDA and EU GMP standards

• Strong documentation and technical skills

Shape the future of pharmaceutical quality at Amaris Consulting in Toronto.
#J-18808-Ljbffr